Patent Application
20180369377
The present invention relates to a novel anti-PD-L1 antibody formulation. In particular, the invention relates to an aqueous pharmaceutical formulation of the anti-PD-L1 antibody Avelumab.
The programmed death 1 (PD-1) receptor and PD-1 ligands 1 and 2 (PD-L1, PD-L2) play integral roles in immune regulation. Expressed on activated T cells, PD-1 is activated by PD-L1 and PD-L2 expressed by stromal cells, tumor cells, or both, initiating T-cell death and localized immune suppression (Dong H, Zhu G, Tamada K, Chen L. B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion. Nat Med 1999; 5:1365-69; Freeman G J, Long A J, Iwai Y, et al. Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation. J Exp Med 2000; 192:1027-34; Dong H, Strome S E, Salomao D R, et al. Tumor-associated B7-H1 promotes T-cell apoptosis: a potential mechanism of immune evasion. Nat Med 2002; 8:793-800. [Erratum, Nat Med 2002; 8:1039; Topalian SL, Drake CG, Pardoll D M. Targeting the PD-1/B7-H1(PD-L1) pathway to activate anti-tumor immunity. Curr Opin Immunol 2012;24:207-12), potentially providing an immune-tolerant environment for tumor development and growth. Conversely, inhibition of this interaction can enhance local T-cell responses and mediate antitumor activity in nonclinical animal models (Dong H, Strome S E, Salomao D R, et al. Nat Med 2002; 8:793-800. [Erratum, Nat Med 2002; 8:1039; Iwai Y, Ishida M, Tanaka Y, et al. Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade. Proc Nati Acad Sci USA 2002; 99:12293-97). In the clinical setting, treatment with antibodies that block the PD-1-PD-L1 interaction have been reported to produce objective response rates of 7% to 38% in patients with advanced or metastatic solid tumors, with tolerable safety profiles (Hamid O, Robert C, Daud A, et al. Safety and tumor responses with lambrolizumab (Anti-PD-1) in melanoma. N Engl J Med 2013; 369:134-44; Brahmer J R, Tykodi S S, Chow L Q, et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med 2012; 366(26):2455-65; Topalian S L, Hodi F S, Brahmer J R, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med 2012; 366(26):2443-54; Herbst R S, Soria J-C, Kowanetz M, et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients. Nature 2014; 515:563-67). Notably, responses appeared prolonged, with durations of 1 year or more for the majority of patients.
Avelumab (also known as MSB0010718C) is a fully human monoclonal antibody of the immunoglobulin (Ig) G1 isotype. Avelumab selectively binds to PD-L1 and competitively blocks its interaction with PD-1.
Compared with anti-PD-1 antibodies that target T-cells, Avelumab targets tumor cells, and therefore is expected to have fewer side effects, including a lower risk of autoimmune-related safety issues, as blockade of PD-L1 leaves the PD-L2-PD-1 pathway intact to promote peripheral self-tolerance (Latchman Y, Wood C R, Chernova T, et al. PD-L1 is a second ligand for PD-1 and inhibits T cell activation. Nat Immunol 2001; 2(3):261-68).
Avelumab is currently being tested in the clinic in a number of cancer types including non-small cell lung cancer, urothelial carcinoma, mesothelioma, Merkel cell carcinoma, gastric or gastroesophageal junction cancer, ovarian cancer, and breast cancer.
The amino acid sequences of Avelumab and sequence variants and antigen binding fragments thereof, are disclosed in WO2013079174, where the antibody having the amino acid sequence of Avelumab is referred to as A09-246-2. Also disclosed are methods of manufacturing and certain medical uses.
Further medical uses of Avelumab are described in W02016137985, PCT/IB2016/052748, PCT/US2016/037498, PCT/US2016/053939, U.S. patent application Ser. No. 62/341,921.
WO2013079174 also describes in section 2.4 a human aqueous formulation of an antibody having the amino acid sequence of Avelumab. This formulation comprises the antibody in a concentration of 10 mg/ml, methionine as an antioxidant and has a pH of 5.5.
A formulation study for an aglycosylated anti-PD-L1 antibody of the IgG1 type is described in WO2015048520, where a formulation with a pH of 5.8 was selected for clinical studies.
As Avelumab is generally delivered to a patient via intravenous infusion, and is thus provided in an aqueous form, the present invention relates to further aqueous formulations that are suitable to stabilize Avelumab with its post-translational modifications, and at higher concentrations as disclosed in WO2013079174.
It is frequently observed, however, that in the course of antibody production the C-terminal lysine (K) of the heavy chain is cleaved off. Located in the Fc part, this modification has no influence on the antibody-antigen binding. Therefore, in some embodiments the C-terminal lysine (K) of the heavy chain sequence of Avelumab is absent. The heavy chain sequence of Avelumab without the C-terminal lysine is shown in
A post-translational modification of high relevance is glycosylation.
Most of the soluble and membrane-bound proteins that are made in the endoplasmatic reticulum of eukaryotic cells undergo glycosylation, where enzymes called glycosyltransferases attach one or more sugar units to specific glycosylation sites of the proteins. Most frequently, the points of attachment are NH2 or OH groups, leading to N-linked or O-linked glycosylation.
This applies also to proteins, such as antibodies, which are recombinantly produced in eukaryotic host cells. Recombinant IgG antibodies contain a conserved N-linked glycosylation site at a certain asparagine residue of the Fc region in the CH2 domain. There are many known physical functions of N-linked glycosylation in an antibody such as affecting its solubility and stability, protease resistance, binding to Fc receptors, cellular transport and circulatory half-life in vivo (Hamm M. et al., Pharmaceuticals 2013, 6, 393-406). IgG antibody N-glycan structures are predominantly biantennary complex-type structures, comprising b-D-N-acetylglucosamine (GlcNac), mannose (Man) and frequently galactose (Gal) and fucose (Fuc) units.
In Avelumab the single glycosylation site is Asn300, located in the CH2 domain of both heavy chains. Details of the glycosylation are described in Example 1.
Since glycosylation affects the solubility and stability of an antibody, it is prudent to take this parameter into account when a stable, pharmaceutically suitable formulation of the antibody is to be developed.
Surprisingly, it has been found by the inventors of the present patent application that it is possible to stabilize Avelumab, fully characterized by its amino acid sequence and its post-translational modifications, in a number of aqueous formulations without the presence of an antioxidant, at pH values as low as 5.2.
a: Heavy chain sequence of Avelumab (SEQ ID NO:1)
b: Heavy chain sequence of Avelumab, lacking the C-terminal K (SEQ ID NO:2)
Unless otherwise stated, the following terms used in the specification and claims have the following meanings set out below.
References herein to “Avelumab” include the anti-PD-L1 antibody of the IgG1 type as defined in WO2013079174 by its amino acid sequence, and as defined in the present patent application by its amino acid sequence and by its post-translational modifications. References herein to “Avelumab” may include biosimilars which, for instance, may share at least 75%, suitably at least 80%, suitably at least 85%, suitably at least 90%, suitably at least 95%, suitably at least 96%, suitably at least 97%, suitably at least 98% or most suitably at least 99% amino acid sequence identity with the amino acid sequences disclosed in WO2013079174. Alternatively or additionally, references herein to “Avelumab” may include biosimilars which differ in the post-translational modifications, especially in the glycosylation pattern, herein disclosed.
The term “biosimilar” (also known as follow-on biologics) is well known in the art, and the skilled person would readily appreciate when a drug substance would be considered a biosimilar of Avelumab. The term “biosimilar” is generally used to. describe subsequent versions (generally from a different source) of “innovator biopharmaceutical products” (“biologics” whose drug substance is made by a living organism or derived from a living organism or through recombinant DNA or controlled gene expression methodologies) that have been previously officially granted marketing authorisation. Since biologics have a high degree of molecular complexity, and are generally sensitive to changes in manufacturing processes (e.g. if different cell lines are used in their production), and since subsequent follow-on manufacturers generally do not have access to the originator's molecular clone, cell bank, know-how regarding the fermentation and purification process, nor to the active drug substance itself (only the innovator's commercialized drug product), any “biosimilar” is unlikely to be exactly the same as the innovator drug product.
Herein, the term “buffer” or “buffer solution” refers to a generally aqueous solution comprising a mixture of an acid (usually a weak acid, e.g. acetic acid, citric acid, imidazolium form of histidine) and its conjugate base (e.g. an acetate or citrate salt, for example, sodium acetate, sodium citrate, or histidine) or alternatively a mixture of a base (usually a weak base, e.g. histidine) and its conjugate acid (e.g. protonated histidine salt). The pH of a “buffer solution” will change very only slightly upon addition of a small quantity of strong acid or base due to the “buffering effect” imparted by the “buffering agent”.
Herein, a “buffer system” comprises one or more buffering agent(s) and/or an acid/base conjugate(s) thereof, and more suitably comprises one or more buffering agent(s) and an acid/base conjugate(s) thereof, and most suitably comprises one buffering agent only and an acid/base conjugate thereof. Unless stated otherwise, any concentrations stipulated herein in relation to a “buffer system” (i.e. a buffer concentration) suitably refers to the combined concentration of the buffering agent(s) and/or acid/base conjugate(s) thereof. In other words, concentrations stipulated herein in relation to a “buffer system” suitably refer to the combined concentration of all the relevant buffering species (i.e. the species in dynamic equilibrium with one another, e.g. citrate/citric acid). As such, a given concentration of a histidine buffer system generally relates to the combined concentration of histidine and the imidazolium form of histidine. However, in the case of histidine, such concentrations are usually straightforward to calculate by reference to the input quantities of histidine or a salt thereof. The overall pH of the composition comprising the relevant buffer system is generally a reflection of the equilibrium concentration of each of the relevant buffering species (i.e. the balance of buffering agent(s) to acid/base conjugate(s) thereof).
Herein, the term “buffering agent” refers to an acid or base component (usually a weak acid or weak base) of a buffer or buffer solution. A buffering agent helps maintain the pH of a given solution at or near to a pre-determined value, and the buffering agents are generally chosen to complement the pre-determined value. A buffering agent is suitably a single compound which gives rise to a desired buffering effect, especially when said buffering agent is mixed with (and suitably capable of proton exchange with) an appropriate amount (depending on the pre-determined pH desired) of its corresponding “acid/base conjugate”, or if the required amount of its corresponding “acid/base conjugate” is formed in situ—this may be achieved by adding strong acid or base until the required pH is reached. For example in the sodium acetate buffer system, it is possible to start out with a solution of sodium acetate (basic) which is then acidified with, e.g., hydrochloric acid, or to a solution of acetic acid (acidic), sodium hydroxide or sodium acetate is added until the desired pH is reached.
Generally, a “stabiliser” refers to a component which facilitates maintenance of the structural integrity of the biopharmaceutical drug, particularly during freezing and/or lyophilization and/or storage (especially when exposed to stress). This stabilising effect may arise for a variety of reasons, though typically such stabilisers may act as osmolytes which mitigate against protein denaturation. As used herein, stabilisers are amino acids (i.e. free amino acids not part of a peptide or protein—e.g. glycine, arginine, histidine, aspartic acid, lysine) and sugar stabilisers, such as a sugar polyol (e.g. mannitol, sorbitol), and/or a disaccharide (e.g. trehalose, sucrose, maltose, lactose).
Agents used as buffering agents, antioxidants or surfactants according to the invention, are excluded from the meaning of the term “stabilisers” as used herein, even if they may exhibit, i.a. stabilising activity.
Herein, the term “surfactant” refers to a surface-active agent, preferably a nonionic surfactant. Examples of surfactants used herein include polysorbate (for example, polysorbate 20 (polyoxyethylene (20) sorbitan monolaurate) also known under the tradename Tween 20); poloxamer (e.g. poloxamer 188, a non-ionic triblock copolymers composed of a central hydrophobic chain of polyoxypropylene (poly(propylene oxide)) flanked by two hydrophilic chains of polyoxyethylene (poly(ethylene oxide)), also known under the tradename Lutrol F 68). Herein, the term “stable” generally refers to the physical stability and/or chemical stability and/or biological stability of a component, typically an active or composition thereof, during preservation/storage.
Agents used as buffering agents, antioxidants or stabilisers according to the invention, are excluded from the meaning of the term “surfactants” as used herein, even if they may exhibit, i.a. surfactant activity.
Herein, the term “antioxidant” refers to an agent capable of preventing or decreasing oxidation of the biopharmaceutical drug to be stabilized in the formulation. Antioxidants include radical scavengers (e.g. ascorbic acid, BHT, sodium sulfite, p-amino benzoic acid, glutathione or propyl gallate), chelating agents (e.g. EDTA or citric acid) or chain terminators (e.g. methionine or N-acetyl cysteine). Agents used as buffering agents, stabilisers or surfactants according to the invention, are excluded from the meaning of the term “antioxidants” as used herein, even if they may exhibit, i.a. antioxidative activity.
A “diluent” is an agent that constitutes the balance of ingredients in any liquid pharmaceutical composition, for instance so that the weight percentages total 100%. Herein, the liquid pharmaceutical composition is an aqueous pharmaceutical composition, so that a “diluent” as used herein is water, preferably water for injection (WFI).
Herein, the term “particle size” or “pore size” refers respectively to the length of the longest dimension of a given particle or pore. Both sizes may be measured using a laser particle size analyser and/or electron microscopes (e.g. tunneling electron microscope, TEM, or scanning electron microscope, SEM). The particle count (for any given size) can be obtained using the protocols and equipment outlined in the Examples, which relates to the particle count of sub-visible particles.
Herein, the term “about” refers to the usual error range for the respective value readily known to the skilled person in this technical field. Reference to “about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se. In case of doubt, or should there be no art recognized common understanding regarding the error range for a certain value or parameter, “about” means ±5% of this value or parameter.
Herein, the term “percent share” in connection with glycan species refers directly to the number of different species. For example the term “said FA2G1 has a share of 25% -41% of all glycan species” means that in 50 antibody molecules analysed, having 100 heavy chains, 25-41 of the heavy chains will exhibit the FA2G1 glycosylation pattern.
It is to be appreciated that references to “treating” or “treatment” include prophylaxis as well as the alleviation of established symptoms of a condition. “Treating” or “treatment” of a state, disorder or condition therefore includes: (1) preventing or delaying the appearance of clinical symptoms of the state, disorder or condition developing in a human that may be afflicted with or predisposed to the state, disorder or condition but does not yet experience or display clinical or subclinical symptoms of the state, disorder or condition, (2) inhibiting the state, disorder or condition, i.e., arresting, reducing or delaying the development of the disease or a relapse thereof (in case of maintenance treatment) or at least one clinical or subclinical symptom thereof, or (3) relieving or attenuating the disease, i.e., causing regression of the state, disorder or condition or at least one of its clinical or subclinical symptoms.
In a first aspect, the invention provides a novel aqueous pharmaceutical antibody formulation, comprising:
In a preferred embodiment the formulation does not comprise any antioxidant.
In an embodiment the concentration of Avelumab in the said formulation is about 10 mg/mL to about 20 mg/mL.
In another embodiment the concentration of acetate or histidine in the said formulation is about 10 mM.
In yet another embodiment the concentration of D-mannitol or trehalose in the said formulation is about 280 mM, or for the combination of arginine HCl and glutamic acid, the concentration of arginine HCl is about 150 mM and the concentration of glutamic acid is about 50 mM.
In yet another embodiment the concentration of Poloxamer 188 or Polysorbate 20 in the said formulation is about 0.5 mg/mL.
In yet another embodiment the pH of the said formulation is 5.2 (±0.1) to 5.5 (±0.1).
In a preferred embodiment the said formulation comprises acetate in a concentration of about 10 mM, and does not comprise any other buffering agent.
In another preferred embodiment the said formulation comprises D-mannitol or trehalose in a concentration of about 280 mM, and does not comprise any other stabiliser.
In yet another preferred embodiment the said formulation comprises Polysorbate 20 or Poloxamer 188 in a concentration of about 0.5 mg/mL, and does not comprise any other surfactant.
In an embodiment the said formulation comprises:
In a preferred embodiment the said formulation comprises:
In a preferred embodiment the said formulation consists of:
In a preferred embodiment the said formulation consists of:
In a more preferred embodiment the said formulation consists of:
In another embodiment the said formulation comprises:
In a preferred embodiment the said formulation comprises:
In a preferred embodiment the said formulation comprises:
In a more preferred embodiment the said formulation consists of:
In a more preferred embodiment the said formulation consists of:
In a more preferred embodiment the said formulation consists of:
In a more preferred embodiment the said formulation consists of:
In a preferred embodiment, the said formulation consists of:
In a preferred embodiment, the latter formulation is made by combining:
In a further embodiment, the invention concerns an aqueous pharmaceutical antibody formulation, whose pH is adjusted with sodium hydroxide. Therefore, the formulation consists of Avelumab in a concentration of 20 mg/mL as the active ingredient; and glacial acetic acid, D-mannitol, Polysorbate 20, sodium hydroxide and water for injection as the excipients; wherein the formulation has a pH of 5.0 to 5.6, preferably 5.2 (±0.1).
In a preferred embodiment, the formulation has a osmolality between 270 and 330 mOsm/kg.
In an embodiment said Avelumab in the formulations as described above has the heavy chain sequence of either
In a preferred embodiment, in the Avelumab glycosylation the said FA2 has a share of 44% -54% and said FA2G1 has a share of 25% -41% of all glycan species.
In a preferred embodiment, in the Avelumab glycosylation the said FA2 has a share of 47% -52% and said FA2G1 has a share of 29% -37% of all glycan species.
In a preferred embodiment, in the Avelumab glycosylation the said FA2 has a share of about 49% and said FA2G1 has a share of about 30%—about 35% of all glycan species.
In a preferred embodiment the Avelumab glycosylation further comprises as minor glycan species A2 with a share of <5%, A2G1 with a share of <5%, A2G2 with a share of <5% and FA2G2 with a share of <7% of all glycan species.
In a preferred embodiment, in the Avelumab glycosylation said A2 has a share of 3%-5%, said A2G1 has a share of <4%, said A2G2 has a share of <3% and said
FA2G2 has a share of 5%-6% of all glycan species.
In a preferred embodiment, in the Avelumab glycosylation said A2 has a share of about 3.5%—about 4.5%, said A2G1 has a share of about 0.5%—about 3.5%, said A2G2 has a share of <2.5% and said FA2G2 has a share of about 5.5% of all glycan species.
In an embodiment the said Avelumab in the formulation as described above has the heavy chain sequence of
In an embodiment the Avelumab formulation as described above is for intravenous (IV) administration.
In a second aspect the present invention provides a drug delivery device comprising a liquid pharmaceutical composition as defined herein. Suitably the drug delivery device comprises a chamber within which the pharmaceutical composition resides. Suitably the drug delivery device is sterile.
The drug delivery device may a vial, ampoule, syringe, injection pen (e.g. essentially incorporating a syringe), or i.v. (intravenous) bag.
The aqueous pharmaceutical formulations are parenterally administered, preferably via sub-cutaneous injection, intramuscular injection, i.v. injection or i.v. infusion. The most preferred way of administration is i.v. infusion.
In a preferred embodiment, the drug delivery device is a vial containing the formulation as described above.
In a more preferred embodiment the said vial contains 200 mg avelumab in 10 mL of solution for a concentration of 20 mg/mL.
In an even more preferred embodiment the vial is a glass vial.
In a third aspect, the invention provides a method of treating cancer comprising administering the formulation as described above to a patient.
In an embodiment the cancer to be treated is selected from non-small cell lung cancer, urothelial carcinoma, bladder cancer, mesothelioma, Merkel cell carcinoma, gastric or gastroesophageal junction cancer, ovarian cancer, breast cancer, thymoma, adenocarcinoma of the stomach, adrenocortical carcinoma, head and neck squamous cell carcinoma, renal cell carcinoma, melanoma, and/or classical Hodgkin's lymphoma.
ANOVA Analysis of variance
CD Cicular Dichroism
CE Capillary Electrophoresis
DoE Design of Experiments
DP Drug Product
DS Drug Substance
DSF Differential Scanning Fluorimetry
DTT Dithiothreitol
ESI Electrospray Ionization
HILIC Hydrophilic Interaction Liquid Chromatography
HMWs Higher Molecular Weights
HPLC High Performance Liquid Chromatography
iCE Capillary Isoelectric Focusing
LC Liquid Chromatography
LMWs Lower Molecular Weights
MALDI Matrix-Assisted Laser Desorption Ionization
MS Mass Spectromety
NTU Nephelometry Turbidity Units
OD Optical density
PBS Poly Buffer Saline
PES Polyethersulfone
PVDF Polyvinylidene Fluoride
SDS-PAGE Sodium Dodecyl Sulphate-PolyAcrylamide Gel Electrophoresis
SE Size Exclusion
TOF Time of Flight
UPLC Ultra Performance Liquid Chromatography
RH Residual Humidity
UV Ultraviolet
In order to assess the stability of the antibody formulations tested, and select the best candidates, thermal stress, mechanical stress, light exposure, osmolality, turbidity, protein content, total aggregates, fragmentation, pH, isoforms, circular dichroism, sub-visible particles and biological activity were determined as stability parameters according to the following protocols:
At 40° C.: the samples in the original vial container were incubated in a thermostatic cabinet at a temperature of 40° C.±2° C. (RH 75%±5%) and withdrawn at pre- determined time points.
At 25° C.: the samples in the original vial container were incubated in a thermostatic cabinet at a temperature of 25° C.±2° C. (RH 60%±5%) and withdrawn at pre-determined time points.
The samples in the original vial container were placed on an orbital shaker maintained at 300 rpm for up to 24 hours (room temperature).
The samples in the original vial container were exposed to a light source for 7 hours adjusting the irradiance level in the Suntest machine to 765 W/m2 (radiation wavelength between 320 nm and 800 nm).
Normal human plasma has an osmolality of about 280 mOSm/kg (Medical. Physiology—Principles for Clinical Medicine. Edited by by Rodney A. Rhoades PhD, David R. Bell PhD). In general, solutions with osmolality close to 300 mOsm/kg are to be targeted when developing parenteral formulations. Acceptable ranges (as per product specifications) are 250-400 mOsm/kg.
Here, osmolality was determined by a cryoscopic method determining the freezing point depression of water solutions after addition of solutes. Amount of solutes, and hence the observed osmolality value is proportional to the observed freezing point depression of the compounded solution.
The turbidity of the solutions were determined with a nephelometer with the capability to measure scattered or attenuated light (Hach Lange Model 2100AN). About 3 mL of solution in reduced volume cuvettes were illuminated by an 870±30 nm light emitting diode (LED) assembly. A detector monitors the scattered light and provided the turbidity (NTU) of the solution by comparison with a series of standards of known turbidity.
Protein content was determined via the optical density of solutions (diluted to ˜0.5 mg/mL protein concentration with relevant buffer) at 280 nm and 320 nm in 1 cm path length quartz cuvettes. Assuming a molar extinction coefficient of 1.46 cm2/mg, protein concentration was obtained by applying the formula: (A280-A320)/(1.46 cm2/mg×1 cm).
The amount of aggregates was determined by the SE-HPLC method. A sample volume of 20 μL (sample diluted to about 0.5 mL with PBS) was injected in a TSK gel Super SW3000 4.6 mm×30 cm (cod. 18675) kept at a temperature of 22±5° C. at a flow rate of 0.35 mL/min (mobile phase was 50 mM sodium phosphate +0.4 sodium perchlorate at pH 6.3±0.1). UV detection at 214 nm.
Low molecular species (or fragments) were determined by Bioanalyzer. Samples are analyzed at a concentration ranging between 1.25-3.75 mg/mL (dilutions made with purified water). 34 of each diluted sample were merged with 2 μL of the corresponding sample buffer (with the addition of DTT when tests were conducted under reducing conditions) and 1 μL of a 60 mM maleimide solution. The samples were heated for 5 minutes at 70° C., then 84 μL of purified water were added and the solutions vortexed and spun down. 6 μL were loaded onto the chip (0.25-0.75 μg of protein). The chip was placed into the Agilent 2100 Bioanalyzer and the analysis started within the following five minutes.
Isoforms distribution was determined by iCE. An Fc coated capillary cartridge (100 mm internal diameter and 50 mm length) was used. The separation is conducted using a 100 mM NaOH solution in 0.1% methylcellulose as a cathodic solution and a 80 mM o-phosphoric acid in 0.1% methylcellulose as an anodic solution. The samples were prepared starting from 80 μL of master mix solution (obtained mixing 700 μL of 0.1% methylcellulose, 10 μL of Pharmalyte 5-8, 70 μL of Pharmalyte 8-10.5, 10 μL of a 7.65 pl marker and 10 μL of a 9.77 pl marker), to which the suitable volume of washed Avelumab sample (corresponding to 200 μg of protein after washing to remove formulation components) was added. An amount of purified water corresponding to (120 μL—volume of washed Avelumab sample added at the previous step) is added. The separation is conducted at a detection wavelength of 280 nm setting pre-focusing and focusing times of 1 and 15 minutes respectively and pre-focusing and focusing voltages of 1500 V and 3000 V respectively. Samples were injected at a pressure of 1000 mBar.
pH: was determined by conventional potentiometry.
Investigations on tertiary structure of Avelumab were carried out using a CD spectropolarimeter by Jasco (mod. J810) in the near UV range (320-250 nm). Samples were diluted to 1.5 mg/mL protein concentration with purified water and, once filled in 1 cm-path length quartz cuvettes, analyzed at room temperature, at a scanning speed of 20 nm/min, with a data pitch of 0.5 nm, integration time of 8 s and standard sensitivity.
Sub-visible particles were counted through the technique of light obscuration method using a Pamas SVSS-C particle counter. Samples were diluted 5-fold with purified water to obtain a final volume of at least 25 mL to be tested.
For the long term stability studies described in Example 5 biological activity was measured as an additional stability parameter.
The method used is based on the ability of Avelumab, absorbed on an ELISA plate, to bind in a dose-dependent manner its antigen PD-L1 present on the cell line HEK-293 (hPDL1, permanently transfected with PD-L1). Dosages used were 400, 200, 100, 50, 25, 12.5, 6.25 and 3.12 ng/mL. From the data obtained EC50 values were calculated. The biological activity (potency) of the samples is expressed as the percentage of bioactivity of the sample against the standard and is calculated as follows: Potency (sample) [%]=(EC50 (sample)/EC50 (standard))*100.7.
The present invention also provides a method of manufacturing an aqueous pharmaceutical formulation as defined herein. The method suitably comprises mixing together, in any particular order deemed appropriate, any relevant components required to form the aqueous pharmaceutical formulation. The skilled person may refer to the examples or techniques well known in the art for forming aqueous pharmaceutical formulations (especially those for injection via syringe, or i.v. infusion).
The method may involve first preparing a pre-mixture (or pre-solution) of some or all components (optionally with some or all of the diluent) excluding Avelumab, and Avelumab may then itself (optionally with or pre-dissolved in some of the diluent) be mixed with the pre-mixture (or pre-solution) to afford the aqueous pharmaceutical formulation, or a composition to which final components are then added to furnish the final aqueous pharmaceutical formulation. Preferably, the method involves forming a buffer system, suitably a buffer system comprising a buffering agent as defined herein. The buffer system is suitably formed in a pre-mixture prior to the addition of Avelumab. The buffer system may be formed through simply mixing the buffering agent (supplied ready-made) with its acid/base conjugate (suitably in appropriate relative quantities to provide the desired pH—this can be determined by the skilled person either theoretically or experimentally). In the case of an acetate buffer system, this means e.g. mixing sodium acetate with HCl, or mixing acetic acid with NaOH or acetate. The pH of either the pre-mixture of final aqueous pharmaceutical formulation may be judiciously adjusted by adding the required quantity of base or acid, or a quantity of buffering agent or acid/base conjugate.
In certain embodiments, the buffering agent and/or buffer system is pre-formed as a separate mixture, and the buffer system is transferred to a precursor of the aqueous pharmaceutical formulation (comprising some or all components save for the buffering agent and/or buffer system, suitably comprising Avelumab and potentially only Avelumab) via buffer exchange (e.g. using diafiltration until the relevant concentrations or osmolality is reached). Additional excipients may be added thereafter if necessary in order to produce the final liquid pharmaceutical composition. The pH may be adjusted once or before all the components are present.
Any, some, or all components may be pre-dissolved or pre-mixed with a diluent prior to mixing with other components.
The final aqueous pharmaceutical formulation may be filtered, suitably to remove particulate matter. Suitably filtration is through filters sized at or below 1 μm, suitably at 0.22 μm. Suitably, filtration is through either PES filters or PVDF filters, suitably with 0.22 μm PES filters.
The person of skill in the art is well aware how an aqueous pharmaceutical formulation can be used to prepare an IV solution, so that the antibody drug substance can be administered intravenously.
The preparation of the IV solution typically consists of a certain amount of solution being withdrawn from saline bags (e.g. 0.9% or 0.45% saline) with a plastic syringe (PP) and a needle and replaced with aqueous pharmaceutical formulation. The amount of solution replaced will depend on the body weight of the patients.
Avelumab is an IgG with two heavy and two light chain molecules. The amino acid sequences of the two chains are shown in
LC-MS and MS/MS methods were used to confirm the intact chains of the molecule and the presence of post-translational modifications to the proteins. The secondary structure of the Avelumab molecule subunits are shown in
As confirmed by UPLC-Q-TOF mass spectrometry of peptides obtained by trypsin digestion, the disulfide bonds Cys21-Cys96,Cys21-Cys90, Cys147-Cys203, Cys138-Cys197, Cys215-Cys223, Cys229-Cys229, Cys232-Cys232, Cys264-Cys324 and Cys370-Cys428 are forming the nine typical IgG bonding pattern.
The molecule contains one N-glycosylation site on Asn300 of the heavy chain. As determined by peptide mapping, the main structure identified by MALDI-TOF was a complex, biantennary type core fucosylated oligosaccaride with zero (GOF), one
(G1F), or two galactose (G2F) residues.The main species are GOF and G1F. Avelumab glycans fluorescence labeled by 2-aminobenzamide have been analysed by HILIC-UPLC-ESI-Q-TOF.
The glycan nomenclature used follows the Oxford Notation as proposed by Harvey et al. (Proteomics 2009, 9, 3796-3801). In species containing fucose (FA2, FA2G1, FA2G2), the Fuc-GlcNAc connectivity is a1-6. In species having a terminal GlcNAc, the GlcNAc-Man connectivity is 81-2. In species containing galactose, the Gal-GlcNAc connectivity is β1-4.
The reported chromatographic profile has been integrated and yielded the Glycan Species Distribution of Avelumab as shown in Table 2a.
The glycan mapping analysis confirmed the identification carried out by peptide mapping (that allowed to identify the two main glycan species), in addition secondary and minor species were also characterized by this method, specific for glycan analysis.
In another measurement the following Glycan Species Distribution was observed.
A first Design of Experiment screening DoE1 at 10 mg/mL Avelumab assessed the impact of several factors such as varying buffer type/pH, excipients, surfactant type and relevant concentration. The study led to the selection of the optimal conditions which can maximize protein stability.
In DoE1 the following factors were taken into account for investigation:
Table 3 illustrates the selection of DoE1 formulas investigated.
DoE1 allowed a selection of suitable buffer/pH, excipient type and surfactant type to be made, that were used for the subsequent DoE2 study described in Example 3.
1Corresponds to 280 mM
2Corresponds to 150 mM
3Corresponds to 50 mM
4 Formulation disclosed in WO2013079174
The pre-formulated drug substance (DS) (10 (±1) mg/mL Avelumab, 1.36 mg/mL Sodium acetate trihydrate, 51 mg/mL D-Mannitol, 0.21 mg/mL L-Methionine, hydrochloric acid q.b. to pH 5.5) was buffer exchanged by tangential flow filtration (using Pellicon XL Biomax Cassettes with a 10 kDa cut-off) in the three buffers: 10 mM sodium acetate pH 5.0, 10 mM sodium citrate pH 5.0 and 10 mM histidine pH 5.75 until a three-fold volume exchange was achieved. At each step the DS solution was diluted 5-fold with relevant buffer. Final target protein concentration in the exchanged DS material was >10 mg/mL. The required excipients were then added to the relevant buffer-exchanged DS material, pH and final solution weight adjusted to the target so as to obtain the DP compositions listed in Table 3.
The sequence of addition of ingredients to the exchanged DS solutions was as follows:
Add D-Mannitol or Trehalose dihydrate or Arginine HCl+Glutamic acid to the exchanged DS solution, stir until complete dissolution, add L-Methionine and stir until complete dissolution (only for Reference), add Poloxamer 188 or Polysorbate 20 (50 mg/mL stock solution), stir until complete dissolution, check pH and adjust to target with sodium hydroxide.
Drug product (DP) solutions were filled (8 mL) in DINER vials (Schott). Visual inspection during the DS diafiltration process revealed that sodium citrate buffer caused generally higher opalescence, whilst remarkably clearer solutions were obtained when exchanges were made in sodium acetate and in histidine buffers.
In Table 4, the results of the experiments carried out to determine protein recovery, osmolality (Osmomat 030/D, Gonotec) and turbidity of the three DS materials upon buffer exchange are shown. Satisfactory protein recoveries (>89%) and final osmolality values (<61 mOsm/kg) were obtained. Turbidity analyses confirmed the higher opalescence of the DS exchanged in sodium citrate.
The osmolality values of the DP formulations relevant to the DoE1 screening were comprised in the range 299-396 mOsm/kg, with most formulations having osmolalities below around 360 mOsm/kg.
The measurements were carried out at time 0, upon manufacturing completion.
The values obtained were in line with target (acceptable range 250-400 mOsm/Kg). Solutions containing Trehalose dihydrate showing higher values (close to 400 mOsm/kg) due to effect of this ingredient on freezing point and subsequent (apparent) increase in osmolality.
As determined by OD measurements, the time 0 content values were in line with theoretical values (10 mg/mL). No significant changes were observed after 1 month at 40° C.
Total aggregates DoE1 formulations were determined yb SE-HPLC at time 0 and after 2 and 4 weeks of storage at 40° C.
No statistically significant variations in terms of aggregates upon thermal stress at 40° C. could be highlighted, thus indicating that the different matrices tested led to invariant/negligible changes in the aggregation pattern.
Fragmentation by Bioanalyzer (2100 Bioanalyzer, Agilent) in DoE1 formulations was determined at time 0 and after 2 and 4 weeks of storage at 40° C.
The data indicated that:
Turbidity by nephelometry in DoE1 formulations was determined at time 0 and after 2 and 4 weeks of storage at 40° C.
Opalescence/strong opalescence consistently observed in all DP formulations containing citrate as a pH buffering agent.
All formulations in sodium acetate and histidine were found to be clear/slightly opalescent with no significant changes observed over 1 month of storage at 40° C.
No pH changes were observed.
The DoE1 formulations were subjected to 24-hour orbital shaking in vials at 300 rpm (room temperature). Upon stress termination the samples were tested for aggregates and opalescence.
Total aggregates were determined by SE-HPLC after mechanical stress and compared to time 0 results. Negligible changes were observed.
Turbidity of DoE1 formulations was determined by nephelometry (2100AN IS, Hach Lange) after mechanical stress and compared to time 0 results. The data were evaluated by ANOVA and a moderately significant impact deriving from surfactant presence (0.01<p-value<0.05) was observed. Either Tween 20 or Poloxamer 188 can help minimize turbidity changes after mechanical stress.
The DoE1 formulations were subjected to 7-hour irradiation at 765 W/m2 (Suntest CPS, Atlas). Upon light stress termination the samples were tested for aggregates, opalescence, pH and isoforms profile.
Using SE-HPLC (Alliance, Waters) slight variations were observed, most frequently when sodium citrate buffer is used (p-value<0.01).
Sodium acetate and histidine are the buffers to be preferred in order to minimize aggregation changes.
As determined by nephelometry the most evident turbidity increases were typically found in citrate buffer at pH values >5.75 (DoE1-13 and DoE1-16 and DoE1-17).
No changes were observed.
The data obtained in the frame of the thermal, mechanical and light stress were evaluated in order to determine conditions that provide maximal protein resistance against stresses.
The results of the analysis are reported in Table 5.
The extrapolated formulation is highlighted in green (ID#=Extrapolated), whilst the most similar formula in the set of those tested is the DoE1-4, also reported. These data demonstrate that acetate buffer pH 5.0-5.5 provides improved protein stability, and that surfactant presence, such as either Tween 20 or Poloxamer 188, at concentrations higher than 0.2 mg/mL, is also important for improved protein stability in the formulation.
A second DoE screening “DoE2” aimed at fine-tuning the formulations selected upon DoE1 completion and concurrently increasing protein concentration to 20 mg/mL.
With this second formulation screening, six formulations at 20 mg/mL protein concentration varying in excipients (D-Mannitol, Trehalose dihydrate) and surfactant (no surfactant, Poloxamer 188 or Polysorbate 20 at 0.5 mg/mL) in presence of 10 mM sodium acetate buffer pH 5.2 were tested after thermal stress (1 month at 40° C., 8 weeks at 25° C. and 2-8° C.) and mechanical shaking (24 hours at 300 rpm, room temperature). The relevant compositions are listed in Table 6.
The DoE2 study was conducted to comparatively evaluate the effect of D-Mannitol vs. Trehalose dihydrate, and the impact of surfactant (either Tween 20 or Poloxamer 188, or no surfactant) in sodium acetate buffer at pH 5.2, at the increased protein concentration of 20 mg/mL. Two pH 5.5 reference samples have been included in the design: “Reference” with L-Methionine, and a reference formulation without L-Methionine, corresponding to DoE1-8.
The pre-formulated drug substance (DS) (27.1 mg/mL Avelumab in 10 mM sodium acetate pH 5.5) was used. The required excipients were then added to the DS material.
The sequence of addition of ingredients to the DS solution was as follows:
The solutions were weight adjusted to the target with relevant buffer so as to obtain the DP compositions listed in Table 7.
DP solutions were filled (8 mL) in DIN6R vials.
No protein content (OD, Lambda 35, Perkin Elmer) changes observed over 4 weeks at 40° C. (Table 7) and 8 weeks at 25° C. (Table 8).
Total aggregates determined by SE-HPLC over stability at 40° C. and 25° C. are represented in
Fragments were evaluated over 1 month at 40° C. and after 2 months at 25° C. The relevant results are shown in
At 40° C., aside from formulation DoE2-1, which presented an amount of fragments higher than 7% after 1 month, the other formulas were observed to have similar behavior (4-6% in fragments after 1 month) with slightly better performances of formulations DoE2-4, DoE2-5 and DoE2-6 (4.0-4.5% in fragments after 1 month at 40° C.).
At 25° C., similar fragmentation percentages were found after 2 months (4.6-6.1%)
The isoforms profile by iCE280 (Fast IEF Analyzer, Convergent Bioscience) in DoE2 formulations was determined at time 0 and after 4 weeks of storage at 40° C. Upon storage at 40° C. typically increases in the acidic cluster can be determined, while a concurrent decrease in the basic isoforms is observed.
The isoforms profiles were evaluated over 1 month at 40° C. (Table 9) and after 8 weeks at 25° C. (
Comparable variations were observed in all samples at both stressing conditions.
No variations observed after 1 month at 40° C. (Table 8) and 2 months at 25° C. (Table 9).
No variations observed after 1 month at 40° C. (Table 12) and 2 months at 25° C. (Table 13).
CD spectra (J-810 Spectropolarimeter, Jasco) of DoE2 formulations were collected at time 0 and after 4 weeks at 40° C. and 8 weeks at 25° C. in the near UV range. Protein in all formulation generally retains its tertiary structure after 4 weeks at 40° C. and 8 weeks at 25° C.
The sub-visible particles of the DoE2 formulations after 8 weeks of storage at 2-8° C. were determined. The results are shown in Table 14. The values were found within European Pharmacopoeia limits (for solutions supplied in containers with a nominal content of less than 100 mL).
After 24 hours at 300 rpm, slight variations in fragments (Table 15) were observed in all samples (up to 5.0-6.5%) with no specific relation to the specific compositions tested.
No changes were observed after mechanical shaking (Table 16).
No changes were observed after mechanical shaking (Table 17).
No changes were observed after mechanical shaking (Table 18).
These results demonstrate that pH 5.2 (extrapolated from DoE1) does not impact fragmentation and therefore is suitable for use in a stable formulation. Optimal pH for preserving protein stability was demonstrated to be in the range 5.0-5.5 (DoE1). In contrast, pH values of 5.6-5.7 could result in higher fragmentation.
Mannitol and Trehalose dihydrate resulted in similar behavior.
No superiority of Poloxamer 188 over Tween 20 was found.
These results also demonstrate that higher protein concentration (20 mg/mL) in the DoE2 formulation is feasible with no observed or anticipated stability issues.
DoE2: Formulation 3 (the formula most preferred and finally selected for further use at 20 mg/mL) was compared in terms of isoforms profiles to the reference formula at time 0, after 4 weeks at 40° C. and 8 weeks at 25° C. in order to evaluate whether different behavior between the two formulas are present over stability time at different conditions. The results are presented in Table 19.
Also the additional timepoint (8 weeks) at 25° C. highlighted no major issues deriving from the reduced pH with respect to the reference formulation.
As methionine was used in the formulation disclosed in WO2013079174, the present Avelumab formulation development aimed to also clarify the impact of this compound as an antioxidant.
The 10 mg/mL samples (from the DoE1 set) were 2-fold diluted with 200 μL of 6% H2O2, obtaining a final protein concentration of about 5 mg/mL and 3% H2O2, and then incubated 3 h at 5° C. At the end of the incubation the sample was washed versus water by ultracentrifugation using an Amicon Ultra (Millipore) 4 mL 10 kDa (4 washes 1 mL each step). The final protein concentration after Amicon treatment was about 10 mg/mL.
DoE1: Formulation 8 is identical to Reference formula of DoE2, except for the presence of L-Methionine: the forced oxidation with H2O2 (3 hours at 2-8° C.) of the two formulas and following testing by iCE280 (oxidation generally leads to increase in more acidic species in electropherograms) and Bioanalyzer aimed to determine whether any differences arise in the two formulations due to the presence of the antioxidant agent. The results are presented in Tables 20 and 21.
Comparable acidic clusters abundances were observed for the two formulations (with or w/o methionine).
Fragments by Bioanalyzer were also tested for these samples (Table 21): comparable levels of fragmentation were observed for the two formulations (with or w/o methionine).
These results suggest that an antioxidant is not needed to stabilize Avelumab and can, therefore, be omitted from the formulation.
The Avelumab formulations 1, 2, 3, 4 and 5 listed in Table 22 were manufactured and used for a long term stability study. The manufacturing process included a compounding followed by a sterilizing double-filtration step through a 0.22 μm membrane (PES and PVDF filters were tested) before the final filling in vials. Formulation 5 corresponds to the Reference used also in the DoE-1 and -2 studies as described in Example 2 and 3.
Upon manufacturing (time 0), the osmolality was determined and found in line with expected value (range: 320-350 mOsm/kg).
Concerning the stability of the formulations, the study schedule, the storage conditions and the tests to be applied are summarized in Table 23. For each time point the table indicates the storage condition to be tested.
The storage of the samples has been carried out with the vials in the upright position. The study is to be conducted over 1 month at 40° C., 6 months at accelerated conditions (at 25° C.) and 12 months at long term conditions (2-8° C.).
Data were collected at 40° C. (up to 1 month), 25° C. (up to 6 months) and 2-8° C. (up to 12 months).
No changes observed over stability. All solutions remain clearer than clearest standard solution (<Y7). Values within specifications.
All solutions show turbidity comprised in the range of clear solutions (1-3 NTU). Values within specifications.
No changes observed over stability. All solutions show pH values in line with target (5.2±0.1 for formulations 1 to 4 and 5.5±0.1 for Reference DP). Values within specifications.
Concentration of formulations 1 and 2 (target concentration=20 mg/mL) was found in the range 18.7-19.8 mg/mL (within ±10% limits with respect to target) during the study, with no significant changes over time.
Concentration of formulations 3 and 4 and Reference DP (target concentration=10 mg/mL) was found in the range 9.3-10.2 mg/mL during the study; no significant changes found.
Protein content remains therefore unaltered over 12 month stability at 2-8° C. (Values within specifications).
No changes in aggregation over 12 months at 2-8° C. with respect to time 0. Values within specifications.
As shown in
As for sub-visible particles per container, the counts were below the limits set by United States, European and Japanese Pharmacopoeia for solutions for infusion or injection with nominal content of less than 100 mL (6000 per container equal to or greater than 10 μm and 600 per container equal to or greater than 25 μm). The relevant bar charts for the two particle size ranges are shown in
No changes in sub-visible particles upon storage were highlighted.
Bioactivity values were typically in the range 89-110% for all time points tested in the course of the stability study. No decrease observed upon storage.
The results from iCE280 experiments are reported in
None of the physico-chemical properties of the five formulations tested was found to undergo significant changes over the 12 month stability at 2-8° C. This is surprising especially for the isoforms patterns, as in formulations 1 to 4 no methionine is present.
No changes observed over stability. All solutions remain clearer than clearest standard solution (<Y7). Values within specifications.
All solutions show turbidity comprised between 1-3 NTU (clear solutions range). Values within specifications.
No changes observed over stability. All solutions show pH values in line with target (5.2±0.1 for formulations 1-2-3-4 and 5.5±0.1 for Reference DP). Values within specifications.
Concentration of formulations 1 and 2 (target concentration=20 mg/mL) was found in the range 18.5-20.0 mg/mL (within ±10% limits with respect to target) during the study, with no significant changes over time.
Concentration of formulations 3 and 4 and Reference DP (target concentration=10 mg/mL) was found in the range 9.5-10.0 mg/mL during the study; no significant changes found.
Protein content remains therefore unaltered over six-month stability at 25° C. Values within specifications.
No changes in aggregation over six months at 25° C. with respect to time 0. Aggregation lower than specification limit (not more than 5%) was found throughout the study.
The samples showed a time 0 value of LMWs by SDS-PAGE N-RED in the range 11.9-16.2%, followed by step-wise increase at the next point (4 weeks) followed by minor changes over the rest of stability, up to six months (
As for sub-visible particles per container, the counts were below the limits set by United States, European and Japanese Pharmacopoeia for solutions for infusion or injection with nominal content of less than 100 mL (6000 per container equal to or greater than 10 μm and 600 per container equal to or greater than 25 μm). The relevant bar—charts are shown in
No changes in sub-visible particles upon stability at 25° C. were highlighted.
Bioactivity values were typically in the range 90-110% for all time points tested in the course of the stability study. No decreases observed upon stability at 25° C.
The results from iCE280 experiments are reported in
Acidic cluster tends to increase over storage at 25° C. All samples show acidic cluster increase of about +10% after six months at 25° C. and concurrent decrease in main peak (−5% after 6 months) and basic cluster (−5% after 6 months).
Over 6-month stability at 25° C., the five formulations tested showed no changes in terms of protein content, appearance, clarity, pH, aggregates, sub-visible particles and bioactivity with respect to time 0.
Fragments were found to increase by +5 percentage points according to SDS-PAGE N-RED after six-months at 25° C., while no statistically significant changes were highlighted by Bioanalyzer.
Similar behavior in isoforms profile by iCE280: acidic cluster of all formulations tend to increase by +10% over the six month-study, with concurrent decreases in main peak and basic cluster.
No changes observed over stability. All solutions remain clearer than clearest standard solution (<Y7).
No changes observed over stability. All solutions show turbidity comprised of 2 NTU (clear solutions range). Values within specifications.
No changes observed over stability. All solutions show pH values in line with target (5.2±0.1 for formulations 1-2-3-4 and 5.5±0.1 for Reference DP). Values within specifications.
Concentration of formulations 1 and 2 (target concentration=20 mg/mL) was found in the range 18.0-19.0 mg/mL (within ±10% limits with respect to target) during the study, with no tendency towards loss in protein over time. Concentration of formulations 3 and 4 and Reference DP (target concentration=10 mg/mL) was found in the range 9.5-10.0 mg/mL during the study, with no tendency towards loss in protein over time. Values within specifications.
Heat stress is, in conclusion, not detrimental to protein content at the conditions tested (up to 1 month at 40° C.).
No major changes in aggregation were highlighted after 1 month. All values below 1% total aggregates after 1 month (lower than specification limits, that is not more than 5%).
Given the variability of the SDS-PAGE N-RED method (for instance, time 0 values of 11.9 and 14.5 were determined for DP 01-190214 and DP 02-190214 respectively) it can be concluded that no major changes occur during the study at 40° C. (
As for sub-visible particles per container, the counts were abundantly below the limits set by United States, European and JP Pharmacopoeia for solutions for infusion or injection with nominal content of less than 100 mL (6000 per container equal to or greater than 10 μm and 600 per container equal to or greater than 25 μm). Relevant bar charts shown in
No changes in sub-visible particles upon thermal stress were highlighted.
Bioactivity values were typically in the range 99-120% for all time points tested in the course of the stability study. No decrease observed upon thermal stress in the samples.
The results from iCE280 experiments are reported in
Acidic cluster tends to increase over storage at 40° C.
Main peak variations (Fehler! Verweisquelle konnte nicht gefunden werden.) confirmed a slightly better stability of new formulas at 10 mg/mL and identical behavior of the remaining compositions.
Results obtained with basic cluster determination confirmed the above described results.
Up to two weeks, similar behavior was observed in the five compositions. At higher stability times, slight differentiation arises between the 20 mg/mL and the 10 mg/mL Avelumab DP (slightly better resistance in formulas at 10 mg/mL).
At 40° C. (1 month), the five formulations tested showed no changes in terms of protein content, appearance, clarity, pH, aggregates, sub-visible particles and bioactivity with respect to time 0.
Small differences between 10 mg/mL and 20 mg/mL DP formulations highlighted by iCE280 (acidic cluster tends to undergo some increase upon storage, slightly more evident in 20 mg/mL than in 10 mg/mL DP formulations).
All formulations were found to be stable: no significant changes observed in terms of appearance, turbidity (by nephelometry), sub-visible particles, pH, protein content (by OD), aggregation (by SE-HPLC), fragments (by SDS-PAGE N-RED and Bioanalyzer), isoforms profile (by iCE280) and biological activity (by bioassay) with respect to time 0.
No changes in terms of protein content, appearance, clarity, pH, aggregates, sub-visible particles and bioactivity with respect to time 0.
Fragments were found to increase by +5% according to SDS-PAGE N-RED after six-months at 25° C., while no statistically significant changes were highlighted by
Bioanalyzer (a method used as an additional tool to add robustness to conclusions on fragmentation occurrence).
A similar behavior was observed in isoforms profile by iCE280: acidic cluster of all formulations tend to increase by +10% over the six month-study, with concurrent decreases in main peak and basic cluster.
No changes in terms of protein content, appearance, clarity, pH, aggregates, sub-visible particles and bioactivity with respect to time 0,
Small differences between 10 mg/mL and 20 mg/mL DP formulations highlighted by iCE280 (acidic cluster tends to undergo some increase upon storage, slightly more evident in 20 mg/mL than in 10 mg/mL DP formulations)
The following DP compositions were manufactured and their stability studied over a period of 24 months:
Both formulations correspond to formulation DP 01-190214 as shown in Table 22. The only difference is that a fixed amount of 0.3 mg/mL (7.5 mM) of sodium hydroxide was used to yield a pH of 5.2 when combined with 0.6 mg/mL glacial acetic acid. The sole difference between formulations DP 01-160414 and DP 02-160414 is that the latter formulation has a volume of 30 mL per vial, while the former has 10 mL per vial.
Both formulations were double-filtered through a 0.22 μm PVDF membrane, followed by the manual filling in vials. Protein content was tested before and after filtration; the relevant results indicate that no loss of protein occurs upon double aseptic filtration
Stability data up to 24 months (at +5±3° C.) and up to 6 months at +25° C.±2° C. (RH 60%±5%) have been collected on the two formulations in the respective final containers (vials).
At +5±3° C., up to 24 months, no changes in protein content (by OD), HMWs (by SE-HPLC), turbidity (by nephelometry), particles formation (by light obscuration), degree of coloration (by visual inspection), and biopotency were observed. Slight increase in acidic isoforms (+5% observed for all compositions after 2 years). No statistically significant changes were observed in terms of fragmentation by SDS-PAGE N-RED, Bioanalyzer and CE-SDS N-RED.
At +25° C.±2° C. (RH 60%±5%), up to 6 months, no changes in protein content (by OD), HMWs (by SE-HPLC), turbidity (by nephelometry), particles formation (by light obscuration), isoforms profile (by iCE280), degree of coloration (by visual inspection), electrophoretic purity (by SDS/-PAGE RED) and biopotency were observed. Similarly to stability at 5° C., no statistically significant increase in fragmentation was observed at +25° C.±2° C. (RH 60%±5%) (results confirmed by Bioanalyzer).
Holding time before filtration (in bags, up to 24 hours at room temperatures), holding time after filtration (in bags, up to 72 hours at room temperature) and shaking (up to 24 hours at 200 rpm at room temperature) showed no significant changes in protein content, particles formation, aggregates and turbidity, thus indicating no major issues that may arise during standard times of operations typically considered during manufacturing process.
A freeze/thaw study evidenced that the tested formulations can safely be frozen at −80° C. and then allowed to warm up to +5±3° C., or +25° C., with no major changes occurring to the protein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15198233.7 | Dec 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/002040 | 12/5/2016 | WO | 00 |
