Patent Grant
10711066
The present invention is directed towards the field of immunology and the treatment of cancer. More specifically, the present invention relates to anti-canine platelet derived growth factor receptor alpha (cPDGFRA) antibodies to the cPDGFRA and methods of use to treat certain disorders such as osteosarcoma (OSA) in dogs.
Sarcomas are a diverse and relatively rare type of cancer that usually develop in the connective tissue of the body, which include fat, blood vessels, nerves, bones, muscles, deep skin tissues and cartilage. OSA represents about 5% of all cancers in dogs, but is the most common form of canine bone tumor. OSA most often occurs in large and giant breed dogs, typically in middle aged or elderly animals. It is considered a highly aggressive form of cancer and over 90% of clinically significant cases have already micro-metastasized by the time of diagnosis. In dogs, treatment options include radiation and/or chemotherapy, and amputation of the limb. Median survival time with various chemotherapy regimens is about one year, while survival with amputation alone is about three months. Unfortunately, an effective treatment for canine osteosarcoma still remains elusive and there exists a need for more and different therapies that may prove to be effective in treating them.
PDGFRA is a tyrosine kinase receptor that is overexpressed in 70-80% of human OSAs and it may be a suitable target for anti-PDGFRA monoclonal antibody therapy. Because canine OSA shows histopathological and clinical features similar to human OSA, cPDGFRA may also be a suitable therapeutic target for OSA in dogs. It has been demonstrated in immunohistochemical (IHC) studies that cPDGFRA is expressed in 78% of evaluated cases. Further, its ligand canine PDGFA was shown to be expressed in 42% of cases (Maniscalco, et al. Vet J. 2013. 195:41).
Olaratumab (also referred to as IMC-3G3) is a fully human IgG1 monoclonal antibody directed against human PDGFRA with potential antineoplastic activity. Successful treatment of soft tissue sarcomas by using Olaratumab can be found in International Publication No. WO2016/003789, for example. Olaratumab selectively binds to human PDGFRA, blocking the binding of its ligand, PDGF. Signal transduction downstream of PDGFR through the MAPK and PI3K pathways is inhibited, which may result in inhibition of angiogenesis and tumor cell proliferation.
Given that Olaratumab is a fully human monoclonal antibody, chronic administration of Olaratumab, or any other fully human antibody, in dogs would likely elicit the development of anti-drug antibodies leading to increasingly strong immune responses after each subsequent treatment of the canine patient with Olaratumab.
Accordingly, the present invention provides a monoclonal antibody that binds canine platelet derived growth factor receptor alpha (cPDGFRA) and has a light chain variable region (LCVR) and a heavy chain variable region (HCVR), wherein the LCVR comprises complementarity determining regions (CDRs) LCDR1, LCDR2, and LCDR3 and the HCVR comprises CDRs HCDR1, HCDR2, and HCDR3, wherein the amino acid sequence of LCDR1 is given by SEQ ID NO:16, the amino acid sequence of LCDR2 is given by SEQ ID NO: 18, the amino acid sequence of LCDR3 is given by SEQ ID NO: 20, the amino acid sequence of HCDR1 is given by SEQ ID NO: 6, the amino acid sequence of HCDR2 is given by SEQ ID NO: 8, and the amino acid sequence of HCDR3 is given by SEQ ID NO: 10.
In another aspect, the present invention provides a monoclonal antibody having a light chain variable region (LCVR) and a heavy chain variable region (HCVR), wherein the amino acid sequence of the LCVR is given by SEQ ID NO: 14 and the amino acid sequence of the HCVR is given by SEQ ID NO: 4.
In yet another aspect, the present invention provides a monoclonal antibody having a light chain (LC) and a heavy chain (HC), wherein the amino acid sequence of the LC is given by SEQ ID NO: 12 and the amino acid sequence of the HC is given by SEQ ID NO: 1.
In an aspect the present invention discloses anti-cPDGFRA antibodies for use in therapy.
In another aspect the present invention discloses anti-cPDGFRA antibodies for use in the treatment of osteosarcoma in a canine patient.
In yet another aspect, the present invention further relates to the use of an antibody of the invention in the manufacture of a medicament for the treatment of osteosarcoma in a canine patient.
Unless indicated otherwise, the term “antibody” (Ab) refers to an immunoglobulin molecule comprising two heavy chains (HC) and two light chains (LC) interconnected by disulfide bonds. The amino terminal portion of each chain includes a variable region of about 100 to about 110 amino acids primarily responsible for antigen recognition via the complementarity determining regions (CDRs) contained therein. The carboxy-terminal portion of each chain defines a constant region primarily responsible for effector function.
As used herein, the terms “complementarity determining region” and “CDR”, refer to the non-contiguous antigen combining sites found within the variable region of LC and HC polypeptides of an antibody or an antigen-binding fragment thereof.
As used herein, the term “light chain variable region” (LCVR) refers to a portion of a LC of an antibody molecule that includes amino acid sequences of Complementarity Determining Regions (CDRs; i.e., LCDR1, LCDR2, and LCDR3), and Light Framework Regions (LFRWs).
As used herein, the term “heavy chain variable region (HCVR)” refers to a portion of a HC of an antibody molecule that includes amino acid sequences of Complementarity Determining Regions (CDRs; i.e., HCDR1, HCDR2, and HCDR3), and Heavy Framework Regions (HFRWs).
The CDRs are interspersed with regions that are more conserved, termed framework regions (“FRW”). Each LCVR and HCVR is composed of three CDRs and four FRWs, arranged from amino-terminus to carboxy-terminus in the following order: FRW1, CDR1, FRW2, CDR2, FRW3, CDR3, FRW4. The three CDRs of the light chain are referred to as “LCDR1, LCDR2, and LCDR3” and the three CDRs of the HC are referred to as “HCDR1, HCDR2, and HCDR3.” The CDRs contain most of the residues which form specific interactions with the antigen. The numbering and positioning of CDR amino acid residues within the LCVR and HCVR regions is in accordance with known conventions (e.g., Kabat (1991), Chothia (1987), and/or North (2011)). In different embodiments of the invention, the FRWs of the antibody may be identical to the germline sequences, or may be naturally or artificially modified.
In certain embodiments, the anti-cPDGFRA Ab of the present invention is altered to increase or decrease the extent to which the antibody is glycosylated. Addition or deletion of glycosylation sites to an antibody may be conveniently accomplished by altering the amino acid sequence such that one or more glycosylation sites is created or removed.
As used herein, the term “Olaratumab” refers to a fully human IgG1 monoclonal antibody directed against human PDGFR, human PDGFRA, and/or human PDGRFA/PDGFRB heterodimers. Olaratumab may also be referred to herein as “human Olaratumab”. As used herein, the HC amino acid sequence of Olaratumab is represented by SEQ ID NO. 26, and the LC amino acid sequence of Olaratumab is represented by SEQ ID NO. 28. The nucleotide sequences that encode the HC and LC amino acid sequences of Olaratumab are SEQ ID NO. 27 and SEQ ID NO. 28, respectively.
As used herein, the term “kit” refers to a package comprising at least two separate containers, wherein a first container contains a K9-6N6.2 Ab and a second container contains pharmaceutically acceptable carriers, diluents, or excipients. As used herein, the term “kit” also refers to a package comprising at least two separate containers, wherein a first container contains K9-6N6.2 Ab, and another antibody preferably for the treatment of cancers other than lymphomas. A “kit” may also include instructions to administer all or a portion of the contents of these first and second containers to a cancer patient. Optionally, these kits also include a third container containing a composition comprising a known chemotherapeutic agent.
As used herein, the terms “treating,” “to treat,” or “treatment” refers to restraining, slowing, stopping, reducing, or reversing the progression or severity of an existing symptom, disorder, condition, or disease.
As used herein, the term “effective amount” refers to the amount or dose of an anti-cPDGFRA Ab which, upon single or multiple dose administration to the patient, provides an effective response in the patient under diagnosis or treatment.
An effective amount can be readily determined by the use of known techniques and by observing results obtained under analogous circumstances. In determining the effective amount for a patient, a number of factors are considered, including, but not limited to: the species or breed of patient; its size, age, and general health; the specific disease or disorder involved; the degree of or involvement or the severity of the disease or disorder; the response of the individual patient; the particular compound administered; the mode of administration; the bioavailability characteristics of the preparation administered; the dose regimen selected; the use of concomitant medication; and other relevant circumstances.
An anti-cPDGFRA antibody designated K9-6N6.1 was created by cloning the entire HCVR of Olaratumab (SEQ ID NO: 31) in frame to the canine IgB heavy chain constant region (GENBANK: AAL35302) to generate a single cDNA sequence (SEQ ID NO: 23). Additionally, the entire LCVR (SEQ ID NO: 33) of Olaratumab was cloned in frame to the canine Kappa light chain constant region (GENBANK: E02906.1) to generate a single cDNA sequence (SEQ ID NO: 25).
K9-6N6.1 contains variable regions identical to those of the fully human Olaratumab. As depicted in Table 1, Olaratumab and K9-6N6.1 binds to cPDGFRA with an affinity that is about 10 fold lower than that of Olaratumab binding to human PDGFRA.
High Throughput Mutagenesis
Mutagenesis experiments were performed to generate antibodies derived from K9-6N6.1. Mutagenic oligonucleotides were generated using an Excel design template (5′ truncation) in a 96-well format and ordered from Integrated DNA Technologies. Mutagenesis was performed using an optimized Quick Change reaction protocol. Briefly, each well (mutagenesis reaction) of a 96-well plate contained enzymatically digested vector DNA for the expression of HC or LC of K9-6N6.1, KOD Hotstart Polymerase, MgSO4, dNTP and different primers for the generation of single mutations. The plate was placed into a PCR machine with the following program: 95° C. for 2 minutes, followed by 20 cycles at 95° C., 20 sec; 60° C., 10 sec; 68° C., 4 min, and then a final extension at 68° C. for 5 minutes. After PCR, 2 μl of DpnI restriction enzyme and reaction buffer were added to the PCR reaction and incubated at 37° C. for 16 hours, followed by incubation at 70° C. for 30 min to inactivate the DpnI. One μl of DNA was then transformed into 10G chemically competent bacterial cells (Lucigen). DNA from the 96-well plate was prepared using a Qiagen 96-well DNA preparation kit, and subjected to DNA sequence analysis.
A total of 210 single point mutations were generated. The efficiency of mutagenesis was monitored by DNA sequence analysis on randomly selected wells. Among 23 wells selected, 3 wells (13%) had a rate of incorporation of the desired mutation below 75% (37-65%). The rest of wells showed incorporation rates of the desired mutations from 75 to 100%.
Deep-Well Expression of Single Mutants and Pools
DNA was prepared from bacteria transformed with either pooled mutagenesis reactions or DNA from single clones confirmed by sequence analysis. Bacterial cells were inoculated and propagated overnight. DNA was prepared using DirectPrep 96 MiniPrep Kit (Qiagen, cat#27361) following the manufacturer's instructions. Following sequence confirmation, DNA from pools or single clones was used to co-transfect Expi293 cells with the HC or LC from the parental K9-6N6.1. Expression of the resulting IgG molecules was conducted in deep-well plates.
PhyNexus Tip Enrichment
Six days after the transfection and subsequent cell growth, supernatants of the cell cultures were collected. Antibodies in culture supernatants were enriched with PhyNexus ProA Phytip columns using a BioMek automated liquid handling system. Antibody supernatants were loaded in the columns and captured on Protein A resin. After washing twice with PBS, antibodies were eluted from the column with 90 μl of 0.1M Glycine-HCl (pH 2.7), and neutralized with 10 μl of Tris-HCl buffer (pH8.0). Antibody concentrations were determined by Octet on a ProA sensor using an antibody standard of known concentration.
Preliminary Screening
All 210 mutants from the pooled transfection and the parental K9-6N6.1 were assessed for binding and blocking using single point ELISAs. Some of the enriched variants from the pooled mutagenesis demonstrated increased binding and blocking activity, while others showed reduced binding to cPDGFRA compared to the parental K9-6N6.1. From the variants showing improved interaction with the dog receptor, 54 clones were selected for further evaluation using titration assays for binding and blocking.
Confirmation of Binding and Blocking Activity
In the assessment of binding, serially diluted K9-6N6.1 variants (enriched or purified) and the parental antibody were added to plates coated with cPDGFRA-Fc (100 μl at 0.5 μg/ml), and incubated at room temperature for 1 hour. To evaluate blockade of the interaction with ligand, serially diluted variants of K9-6N6.1 (enriched and purified) and the parental K9-6N6.1 antibody were mixed with a fixed amount of biotinylated-cPDGFRA (0.0625 μg/ml) and incubated at room temperature for 1 hour. The mixture was transferred to 96-well plates pre-coated with canine PDGFAA (0.125 μg/ml) and incubated at room temperature for 2 hours. The plates were then washed, detection antibodies were added, and the amount of binding determined as described above.
For assessment of binding and blocking using Olaratumab, the above methods were modified. In the binding ELISA, plates were coated with 100 μl of human PDGFRA at 1 μg/ml, and HRP-Protein L (GenScript) was used for detection. In the blocking assay, 0.5 μg/ml human PDGFRA and 0.5 μg/ml of PDGFAA were used. Plate bound human PDGFRA was detected with a biotinylated anti-human PDGFRA antibody (R&D).
Screening of Mutants Using Binding and Blocking Assays (Single Point ELISA)
Variants from the mutagenesis were initially screened using a single-point ELISA. In the binding assay, 0.5 μg/ml of enriched antibody, either variants of K9-6N6.1 or the parental K9-6N6.1 antibody were added to plates coated with cPDGFRA (100 μl at 0.5 μg/ml) and incubated at room temperature for 1 hour. The plates were washed three times with phosphate buffered saline with Tween® (PBST), and then incubated at room temperature for an additional hour with a goat anti-canine-Fab antibody/horse radish peroxidase (HRP) conjugate (Sigma). After washing three times with PBST, tetramethylbenzidine (TMB) peroxidase substrate was added to the plate. The absorbance at 450 nm was read using a microplate reader.
In the blocking assay, 15 μg/ml of the enriched variants or the parental antibody were first mixed with a fixed amount of biotinylated-cPDGFRA (0.0625 μg/ml) and incubated at room temperature for 1 hour. The mixture was transferred to 96-well plates pre-coated with canine PDGFAA (0.125 μg/ml) and incubated at room temperature for 2 hours. After washing three times with PBST, the plates were incubated with HRP-conjugated streptavidin for 1 hour. The plates were then washed and developed as described above.
Identification of Beneficial Mutations
Results of binding and blocking were analyzed and EC50 (binding) and IC50 (blocking) values were calculated. To estimate improvement of each mutant variant over the parental K9-6N6.1 molecule, fold improvement was calculated as parental EC50 or IC50 divided by variant EC50 or IC50.
As depicted in Table 2, among the variants, HC-Y100D (clone 1F12) showed an almost 17-fold improvement in blocking the binding of canine PDGF-AA to cPDGFRA, but binding was not detected to human PDGFRA. However, a mutation in the LC, S28A (2A2), showed 13-fold improvement in blocking activity compared with the parental antibody, while retaining binding to both human PDGFRA and cPDGFRA. LC-S28A (clone 2A2) is a mutation that improves binding to PDGFRA. The unexpected improvement in binding and blocking activities of HC-Y100D (1F12) and LC-S28A (2A2) were confirmed by using single clones.
Combination of HC-Y100D and LC-S28A
Heavy and light chains of the K9-6N6.1 variants HC-Y100D and LC-S28A were co-expressed to determine the impact on binding and blocking of combining the two mutations. Briefly, the HC expression vector with HC-Y100D (1F12) was co-transfected into HEK293 cells with the LC expression vector containing the S28A (2A2) mutation. Protein was purified with using a ProA column and evaluated in binding and blocking assays. The IC50 of the HC-Y100D and LC-S28A (clone 1F12-2A2) combination antibody indicated an additional two fold improvement over 1F12.
Evaluation of Affinity
The binding kinetics of selected K9-6N6.1 variants to cPDGFRA were measured using a BIAcore T200 instrument (BIAcore, Inc., Piscataway, N.J.). Briefly, a cPDGFRA extracellular domain (ECD)-Fc fusion protein was immobilized on a sensor chip and antibody was injected at various concentrations. Sensograms were obtained at each concentration and evaluated using the BIA Evaluation 3.0 program to determine rate constants. The affinity constant (KD) was calculated from the ratio of rate constants Koff/Kon. The evaluation was performed at 25° C. As depicted in Table 3, kinetic evaluation showed that overall affinities are improved over parent K9-6N6.1, 5-fold for 1F12 (Y100D) and 12-fold for 1F12-2A2 (Y100D and S28A).
Removal of Deamidation Site in K9-6N6.1
The amino acid sequence of the IgG-B portion of K9-6N6.1 contains an asparagine residue at position 232 is followed by glycine, a small, flexible residue (G233). The NG pairing in exposed regions of proteins often yields high levels of deamidation. Biophysical evaluation of K9-6N6.1 revealed that about twenty percent of the generated antibody was undergoing deamidation of N232 (asparagine 232) in the hinge region of the antibody.
To eliminate the occurrence of deamidation of K9-6N6.1, site-directed mutagenesis was used to replace N232 with aspartic acid (D), serine (S), or glutamine (Q). The substitutions were based on similarity of the side chain to that of asparagine and included consideration of size, polarity, and type. A standard mutagenesis protocol was used. Mutations were confirmed by DNA sequencing. Mutated antibodies were expressed using transiently transfected HEK293 cells and purified with protein A columns. Purified proteins were then evaluated using binding and blocking assays (ELISA) and the results were compared to the parental K9-6N6.1 as a control.
Selection of N232S
As depicted in Table 4, all three N232 variants retained the binding and blocking activity of the parental K9-6N6.1, with EC50 values ranging from 0.19 to 0.21 nM and IC50 values from 27 to 36 nM. In addition, qPCR (quantitative polymerase chain reaction) was used to assess the thermostability of the mutated antibodies. The results showed that the thermostability of all three variants was unchanged relative to the parental K9-6N6.1. Serine is less likely to undergo post-translational modification than aspartic acid and glutamine. Serine was selected as the replacement for asparagine at position 232.
Removal of N-Linked Glycosylation Site in K9-6N6.1
Mammalian cells are capable of generating post-translational modifications to antibodies, this includes glycosylation, typically at N or O-linked sites. The sequence N-x-S/T is often a site at which glycosylation occurs through post-translational modification. For monoclonal antibodies, there is typically only a single N-linked site within the CH2 region of the heavy chain constant region (typically at N297 for human IgGs). For monoclonal antibodies the presence and content of this N-linked glycosylation may contribute to its ability to bind to Fc receptors and mediate immune effector function. As a result of the production process in cultured cells, the extent and content of glycans added to N-linked sites can vary, and contribute to the heterogeneity, and potential activity (if effector function is important) of the product.
Depending on its location within a CDR sequence and the extent of glycosylation, the presence of additional N-linked sites within variable regions of monoclonal antibodies may impact its potency and can also contribute to product heterogeneity during manufacture. Depending on the host cell used for production (e.g. mouse NSO cells), these “Fab” or V-region glycosylation sites may be preferentially glycosylated with atypical glycans which can elicit an immune hypersensitivity response.
For replacement of N-linked sites, Q (glutamine) is typically used as a conservative amino acid substitution that removes the consensus sequence for glycosylation. Thus, using standard mutagenesis techniques, a N30Q residue substitution was made within the HCDR1 of K9-6N6.1. The N30Q substitution did not substantially affect the binding to receptor as compared to the parental K9-6N6.1.
K9-6N6.2 Sequence
K9-6N6.2 is derived from K9-6N6.1. K9-6N6.2 contains two substitutions to the K9-6N6.1 parent molecule, VH-Y100D and VL-S28A, that improve affinity, as well as two substitutions, N30Q and N232S, that add stability and result in fewer post translational modifications than in the K9-6N6.1 parent antibody.
SEQ ID NO: 1 is the amino acid sequence of the HC of K9-6N6.2.
SEQ ID NO: 2 corresponds to the nucleotide sequence that encodes for the amino acid sequence corresponding to SEQ ID NO: 1 and also contains a DNA coding sequence for a murine heavy chain leader, as well as DNA coding sequences for restriction enzymes HindIII and EcoRI.
SEQ ID NO: 3 is the translated amino acid sequence of SEQ ID NO: 2 and contains the HC of K9-6N6.2.
SEQ ID NO: 4 is the amino acid sequence of the HCVR of K9-6N6.2.
SEQ ID NO: 5 is the nucleotide sequence encoding the HCVR of K9-6N6.2.
SEQ ID NO: 6 is the heavy chain CDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 7 is the nucleotide sequence encoding the HCDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 8 is the HCDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 9 is the nucleotide sequence encoding the HCDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 10 is the HCDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 11 is the nucleotide sequence encoding the HCDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 12 is the LC amino acid sequence of K9-6N6.2.
SEQ ID NO: 13 is the nucleotide sequence encoding the LC of K9-6N6.2.
SEQ ID NO: 14 is the amino acid sequence of the LCVR of K9-6N6.2.
SEQ ID NO: 15 is the nucleotide sequence encoding the LCVR of K9-6N6.2.
SEQ ID NO: 16 is the LCDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 17 is the nucleotide sequence encoding the LCDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 18 is the LCDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 19 is the nucleotide sequence encoding the LCDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 20 is the LCDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 21 is the nucleotide sequence encoding the LCDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 22 is the HC amino acid sequence of K9-6N6.1.
SEQ ID NO: 23 is the nucleotide sequence encoding the HC amino acid sequence of K9-6N6.1.
SEQ ID NO: 24 is the LC amino acid sequence of K9-6N6.1.
SEQ ID NO: 25 is the nucleotide sequence encoding the LC amino acid sequence of K9-6N6.1.
SEQ ID NO: 26 is the HC amino acid sequence of Olaratumab.
SEQ ID NO: 27 is the nucleotide sequence encoding the HC amino acid sequence of Olaratumab.
SEQ ID NO: 28 is the LC amino acid sequence of Olaratumab.
SEQ ID NO: 29 is the nucleotide sequence encoding the LC amino acid sequence of Olaratumab.
SEQ ID NO: 30 is the HCVR amino acid sequence of Olaratumab.
SEQ ID NO: 31 is the nucleotide sequence encoding the HCVR amino acid sequence of Olaratumab.
SEQ ID NO: 32 is the LCVR amino acid sequence of Olaratumab.
SEQ ID NO: 33 is the nucleotide sequence encoding the LCVR amino acid sequence of Olaratumab.
SEQ ID NO: 34 is the HCDR1 amino acid sequence of Olaratumab.
SEQ ID NO: 35 is the HCDR2 amino acid sequence of Olaratumab.
SEQ ID NO: 36 is the HCDR3 amino acid sequence of Olaratumab.
SEQ ID NO: 37 is the LCDR1 amino acid sequence of Olaratumab.
SEQ ID NO: 38 is the LCDR2 amino acid sequence of Olaratumab.
SEQ ID NO: 39 is the LCDR3 amino acid sequence of Olaratumab.
Method for Making K9-6N6.2
K9-6N6.2 was engineered for expression utilizing glutamine synthetase (GS) expression plasmids for use in mammalian cells. The cDNAs encoding the heavy and the light chains were cloned into expression cassettes regulated by the viral CMV promoter and SV40 transcriptional terminator and polyadenylation 3′ UTR. Both cassettes were contained on a single plasmid, along with an expression cassette for the selectable GS marker. For K9-6N6.2, the expression plasmid was first evaluated in transient expression in CHO cells utilizing a lipid-based transfection process (ExpiCHO; ThermoFisher). For cell line generation, CHO cells were electroporated with the K9-6N6.v2 expression vector and clones selected in media lacking glutamine in the presence of the inhibitor methionine sulfoximine. Following clone selection, cell lines were evaluated for production titer, with clones reaching 1 g/L or higher selected for production. The selected production line was expanded and a frozen cell bank established for production of the monoclonal antibody K9-6N6.2. For material produced from transient or stable transfection, K9-6N6.2 was purified by Pro-A affinity chromatography.
SEQ ID NO: 1 is the amino acid sequence of the heavy chain of K9-6N6.2.
SEQ ID NO: 2 is the nucleotide sequence that encodes for the amino acid sequence corresponding to SEQ ID NO: 1 and also contains a DNA coding sequence for a murine heavy chain leader, as well as DNA coding sequences for restriction enzymes HindIII and EcoRI.
SEQ ID NO: 3 is the translated amino acid sequence of SEQ ID NO: 2 and contains the heavy chain of K9-6N6.2.
SEQ ID NO: 4 is the amino acid sequence of the heavy chain variable region of K9-6N6.2.
SEQ ID NO: 5 is the nucleotide sequence encoding the heavy chain variable region of K9-6N6.2.
SEQ ID NO: 6 is the heavy chain CDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 7 is the nucleotide sequence encoding the heavy chain CDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 8 is the heavy chain CDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 9 is the nucleotide sequence encoding the heavy chain CDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 10 is the heavy chain CDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 11 is the nucleotide sequence encoding the heavy chain CDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 12 is the light chain amino acid sequence of K9-6N6.2.
SEQ ID NO: 13 is the nucleotide sequence encoding the light chain of K9-6N6.2.
SEQ ID NO: 14 is the amino acid sequence of the light chain variable region of K9-6N6.2.
SEQ ID NO: 15 is the nucleotide sequence encoding the light chain variable region of K9-6N6.2.
SEQ ID NO: 16 is the light chain CDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 17 is the nucleotide sequence encoding the light chain CDR1 amino acid sequence of K9-6N6.2.
SEQ ID NO: 18 is the light chain CDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 19 is the nucleotide sequence encoding the light chain CDR2 amino acid sequence of K9-6N6.2.
SEQ ID NO: 20 is the light chain CDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 21 is the nucleotide sequence encoding the light chain CDR3 amino acid sequence of K9-6N6.2.
SEQ ID NO: 22 is the heavy chain amino acid sequence of K9-6N6.1.
SEQ ID NO: 23 is the nucleotide sequence encoding the heavy chain amino acid sequence of K9-6N6.1.
SEQ ID NO: 24 is the light chain amino acid sequence of K9-6N6.1.
SEQ ID NO: 25 is the nucleotide sequence encoding the light chain amino acid sequence of K9-6N6.1.
SEQ ID NO: 26 is the heavy chain amino acid sequence of Olaratumab.
SEQ ID NO: 27 is the nucleotide sequence encoding the heavy chain amino acid sequence of Olaratumab.
SEQ ID NO: 28 is the light chain amino acid sequence of Olaratumab.
SEQ ID NO: 29 is the nucleotide sequence encoding the light chain amino acid sequence of Olaratumab.
SEQ ID NO: 30 is the heavy chain variable region amino acid sequence of Olaratumab.
SEQ ID NO: 31 is the nucleotide sequence encoding the heavy chain variable region amino acid sequence of Olaratumab.
SEQ ID NO: 32 is the light chain variable region amino acid sequence of Olaratumab.
SEQ ID NO: 33 is the nucleotide sequence encoding the light chain variable region amino acid sequence of Olaratumab.
SEQ ID NO: 34 is the heavy chain CDR1 amino acid sequence of Olaratumab.
SEQ ID NO: 35 is the heavy chain CDR2 amino acid sequence of Olaratumab.
SEQ ID NO: 36 is the heavy chain CDR3 amino acid sequence of Olaratumab.
SEQ ID NO: 37 is the light chain CDR1 amino acid sequence of Olaratumab.
SEQ ID NO: 38 is the light chain CDR2 amino acid sequence of Olaratumab.
SEQ ID NO: 39 is the light chain CDR3 amino acid sequence of Olaratumab.
The present application is a national phase entry under 35 U.S.C. § 371 of International Patent Application PCT/US2017/042996, filed on Jul. 20, 2017 and published in English as International Patent Publication WO2018/022407A1 on Feb. 1, 2018, which claims benefit of priority to U.S. Pat. App. Ser. No. 62/367,808 filed Jul. 28, 2016; all of which are incorporated by reference in their entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2017/042996 | 7/20/2017 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2018/022407 | 2/1/2018 | WO | A |
| Number | Date | Country |
|---|---|---|
| 2006138729 | Dec 2006 | WO |
| 2016003789 | Jan 2016 | WO |
| Entry |
|---|
| Arico et al. J. Comp. Path. 151: 322-328, 2014. |
| Patent Cooperation Treaty International Search Report and the Written Opinion of the International Searching Authority pertaining to International Application No. PCT/2017/042996; dated Sep. 29, 2017. |
| Maniscalco, Lorella, et al. “PDGFs and PDGFRs in canine osteosarcoma: new targets for innovative therapeutic strategies in comparative oncology.” The Veterinary Journal 195, No. 1 (2013): 41-47. |
| Kabat et al., Sequences 20 of Proteins of Immunological Interest, Fifth Edition, U.S. Department of Health and Human Services, NIH Publication No. 91-3242 (1991). |
| Chothia, Cyrus, and Arthur M. Lesk. “Canonical structures for the hypervariable regions of immunoglobulins.” Journal of molecular biology 196, No. 4 (1987): 901-917. |
| North et al., A New Clustering of Antibody CDR Loop Conformations, Journal of Molecular Biology, 406:228-256 (2011). |
| Number | Date | Country | |
|---|---|---|---|
| 20190300612 A1 | Oct 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62367808 | Jul 2016 | US |
