The present invention generally relates to a drug delivery device adapted to receive a drug filled cartridge and expel a dose therefrom.
In the disclosure of the present invention reference is mostly made to the treatment of diabetes, however, this is only an exemplary use of the present invention.
The most common type of injection devices adapted to receive a drug filled cartridge (also termed reservoir or container) and expel a dose therefrom are generally pen-formed and utilizes a so-called cartridge holder adapted to receive and mount a cartridge in the device. Correspondingly, most pen-formed drug delivery devices comprises a generally cylindrical cartridge holder for receiving and holding a generally cylindrical drug-filled cartridge in a mounted position, the cartridge comprising a proximally facing and axially displaceable piston, and a main body with a housing in which a drug expelling mechanism is arranged, the mechanism comprising an axially displaceable piston rod adapted to engage the piston of a mounted cartridge to thereby expel a dose of drug from the cartridge. Between the cartridge holder and the main body coupling means is provided allowing a user to remove the cartridge holder from the main body and reattach it when a used cartridge has been exchanged with a new cartridge. The cartridge is inserted in the cartridge holder by axial movement through a proximal opening. The coupling means may be in the form of a threaded connection or a bayonet coupling. Depending on the design of the drug delivery device the piston rod in a durable device has to be moved proximally (i.e. “reset”) by rotation when an empty cartridge is exchanged with a full cartridge, or the piston rod can be reset by being pushed axially, e.g. by unlocking the piston rod when the cartridge holder is removed from the main body, this as disclosed in e.g. US 2009/0275914 and WO 2011/051366. WO 2004/020026 discloses a pen device comprising a front loaded cartridge holder in which the cartridge is prevented from moving distally by a pair of user-operated gripping arms.
Whereas the cartridge holder and the interface with the main body can be manufactured with narrow tolerances, the cartridges in most cases comprise a main cylindrical body manufactured from glass and thus inherently have very wide tolerances. Correspondingly, the parts of a drug delivery device adapted to receive and interface with such a cartridge has to allow relatively large tolerances of the glass part, especially lengthwise, yet providing functionality and dosing accuracy which is not influenced by length variations of the cartridge. To provide this most devices are designed to axially fixate a received cartridge.
Some of the reasons for providing a mechanism that safely fixes a user exchangeable cartridge part to a reusable (durable) part are: (1) if the exchangeable part is not safely axially fixed to the reusable part it may rattle which may lead to reduced perceived quality and possibly increases the risk of cracks and breakage of the drug cartridge. (2) If the exchangeable part is not safely axially fixed to the reusable part it may be possible for the user to push the drug cartridge towards the expelling mechanism in the reusable part of the device. Depending on the design of the expelling mechanism such a movement may lead to unintended out-dosing of drug.
This issue has been addressed in a number of ways in the past. For example, the drug delivery device may be provided with mechanical stop surfaces that restrict distal movement of the exchangeable part, and a spring that makes it difficult to push the exchangeable part in the proximal direction, however, this design still makes it possible to move the exchangeable part in the proximal direction if the user exceeds the spring force. This design is utilized in e.g. HumePen® from Lilly. The issue regarding the risk of unintended out-dosing can be reduced by a relatively large spring force, just as when the user (correctly) mounts a needle assembly, the possible proximal movement of the exchangeable part can be restricted due to stop surfaces between the needle assembly hub and the cartridge holder. However if the user only mounts the needle assembly partially, it is still possible to perform an unintended out-dosing due to proximal movement of the drug cartridge. Another method of reducing the user's possibility to move the drug cartridge is by means of mechanical stop surfaces that restrict distal movement of the exchangeable part, and a transparent cartridge holder with no openings that encapsulates the drug cartridge. This design reduces the user's possibility to push the drug cartridge in the proximal direction, however, it does not eliminate the issues about rattling of the cartridge. This design is utilized in e.g. the ClikStar® pen device from Sanofi Aventis.
WO 2011/067269 discloses a further alternative in which axial movement of the drug cartridge is restricted by means of a snap interface between the cartridge and the cartridge holder, which engages the drug cartridge corresponding to its neck portion. For a durable device this solution requires that the user presses the cartridge onto the snap, and that the user can de-snap the cartridge before exchanging it. WO 2011/092326 discloses a cartridge holder comprising a coupling which engages and axially fixes a loaded cartridge when a needle assembly is mounted on the cartridge holder.
WO 2008/062025 discloses a yet further alternative in which axial movement of the drug container is restricted by means of a cartridge assembly in which the cartridge part and the cartridge holder with the coupling means are provided as a single disposable unit. The cartridge assembly may comprise a conventional glass cartridge enclosed in a polymeric enclosure or the cartridge assembly may have a generally integral design formed from a polymeric material. The latter type of design is also disclosed in WO 00/02605. In the OptiClik® pen device from Sanofi a disposable cartridge assembly is used in which also the piston rod is provided as part of the cartridge assembly.
Having regard to the above, it is an object of the present invention to provide a drug delivery device adapted to receive and hold a drug-filled cartridge in a simple and effective way, the arrangement being user-friendly, cost-effective and reliable.
In the disclosure of the present invention, embodiments and aspects will be described which will address one or more of the above objects or which will address objects apparent from the below disclosure as well as from the description of exemplary embodiments.
Thus, in accordance with a first aspect of the invention a drug delivery system is provided comprising a cartridge, a cartridge holder and an expelling assembly, the cartridge comprising a cylindrical body portion having opposed distal and proximal portions, an axially displaceable piston arranged in the body portion, a distal outlet portion, a drug-filled variable volume reservoir being provided by the body portion and the piston, and first coupling means arranged at the distal portion. The cartridge holder is front-loaded and adapted to axially receive and hold the cartridge in a loaded position, and comprises a distal portion with a distal opening adapted to receive the cartridge in a proximal direction (i.e. the proximal portion of the cartridge is inserted through the cartridge holder distal opening in a proximal direction), and second coupling means arranged at the distal portion, wherein the first and second coupling means are configured to engage each other to thereby axially lock the received cartridge in the cartridge holder. The expelling assembly is adapted to engage and axially displace the piston in a loaded cartridge in a distal direction to thereby expel a dose of drug from the cartridge. The expelling assembly may be arranged in a housing providing an outer shell of a drug delivery device or it may be in the form of an assembly formed integrally with a housing. The cartridge holder may be formed integrally with the housing or be attached.
By this arrangement one or more of the following advantages can be achieved: Relatively easy integration of the coupling parts, no rattling of the cartridge in the cartridge holder, no risk of unintended out-dosing due to proximal movement of the cartridge, allows large production tolerances of the drug cartridge (e.g. a glass cartridge may actually be manufactured having larger tolerances than used today, this potentially saving costs), no need for a spring to make automatic adaption to the drug cartridge, possible to make an easy and intuitive solution for the user for attaching and releasing the cartridge, as well as enabling mechanical coding between the reusable part and the exchangeable part.
The coupling means could be designed in various ways. For example, the first and second coupling means could be configured as cooperating rotational coupling means allowing a cartridge to be secured to the cartridge holder by relative rotational movement there between, or the first and second coupling means could be configured as cooperating axial snap coupling means allowing a cartridge to be secured to the cartridge holder by relative axial movement there between. Such a snap coupling could also incorporate a biasing structure being strained when the cartridge is snapped in place, this allowing the cartridge to be pushed out when the coupling is released by the user. Alternatively or in addition, the second coupling means may comprise user operated locking means for securing a cartridge in the mounted position. The rotational coupling may comprise an axial component and the axial snap coupling may comprise a rotational component.
The cartridge may be provided with a needle interface allowing a needle assembly to be mounted in fluid communication with the reservoir. Alternatively the needle interface may be formed as part of the cartridge holder.
The cartridge may comprise a body part forming the cylindrical body portion with the needle interface and the first coupling means being attached at the distal outlet portion, e.g. in the form of an integral coupling part forming the needle interface and the first coupling means. The body part may comprise a distal neck portion with an opening closed by a needle penetreble septum, the integral coupling part being attached corresponding to the neck portion. The septum may be secured to the neck portion by a circumferential member to which the integral coupling part is attached. Alternatively, the cylindrical body portion, the needle interface and the first coupling means may be formed integrally from a polymeric material.
In a shorter wording the present invention provides a drug delivery system comprising a drug-filled cartridge, a drug delivery device with a front-loaded cartridge holder adapted to axially receive and hold the cartridge in a loaded position, the cartridge holder comprising a distal opening adapted to receive the cartridge in a proximal direction, wherein the cartridge and the cartridge holder are provided with coupling means configured to engage each other to thereby axially lock the received cartridge in the cartridge holder. The cartridge and drug delivery device may comprise additional specific features as disclosed above.
In a further aspect of the invention a drug cartridge is provided comprising a cylindrical body portion, an axially displaceable piston, a distal outlet portion, a variable volume reservoir being provided by the body portion and the piston, first coupling means allowing a needle assembly to be mounted in fluid communication with the reservoir, and second coupling means allowing the cartridge to be attached to a cartridge holder of a drug delivery device. The first coupling means may comprise a (first) thread or bayonet coupling, and the second coupling means may comprise a (second) thread or bayonet coupling. The diameter of the thread or bayonet coupling of the first coupling means will typically be smaller than diameter of the thread or bayonet coupling of the second coupling means. Otherwise the cartridge may be formed as describe above.
In a yet further aspect of the invention a system is provided comprising first and second drug delivery devices each configured as disclosed above as well as first and second cartridges each configured as disclosed above, wherein the first device and the first cartridge comprise a pair of corresponding first key structures allowing the first cartridge to be received and held in the cartridge holder of the first device, and the second device and the second cartridge comprise a pair of corresponding second key structures allowing the second cartridge to be received and held in the cartridge holder of the second device, and wherein the key structures prevents that the first cartridge can be received and held in the second cartridge holder and that the second cartridge can be received and held in the first cartridge holder. The cartridge may comprise an integral coupling part forming the needle interface and the first coupling means as well as the cartridge key structures.
By this arrangement drugs can be supplied in different concentrations and in correspondingly coded cartridges adapted to be received in drug delivery devices specifically adapted for a given concentration, the system preventing that a given cartridge is mounted in a device not adapted for the drug formulation of that specific cartridge. For example, insulin may be provided in concentrations of 100 IU/ml and 200 IU/ml and in cartridges coded to ensure that a given insulin can only be used in combination with a correspondingly adapted drug delivery device.
As the piston rod in a front loaded device normally is not directly accessible to the user and thereby cannot easily be rotated or pushed back to an initial position, this type of device is normally designed to allow the piston rod to be pushed proximally when a new cartridge is inserted, e.g. as disclosed in WO 2004/020026. By using the piston in the cartridge to push back the piston rod a potential initial air gap between the piston of a new cartridge and the piston-engaging distal end of the piston rod can ideally be eliminated as the piston and piston rod will be interfaced during the cartridge insertion movement, this eliminating the need for the user to manually forward the piston rod after cartridge change. Indeed, this will only work if the piston in the new cartridge is positioned more proximal than the piston of the cartridge it is replacing and if the piston rod has not accidentally been manipulated. If this is not the case a gap may be formed between a newly loaded used cartridge and the piston rod.
Thus, in accordance with a yet further aspect of the invention a drug device is provided comprising a housing and a holder for receiving and holding a cartridge (e.g. a replaceable drug-filled reservoir) in a loaded position, the holder having a generally tubular configuration with a distal opening adapted to axially receive the cartridge, the cartridge comprising an axially displaceable piston having an initial proximal position, a fully-forwarded distal position, and an intermediate position there between (i.e. any position between the two other defined positions). The device is further provided with drug expelling means comprising an axially displaceable piston rod adapted to engage the piston of a loaded reservoir, the piston rod being moveable between a proximal loaded position and a distal-most position, wherein a loading position is defined distally of the proximal position. In such an arrangement the piston rod, when positioned proximally of the loading position, is adapted to be moved to its loading position when a cartridge is removed from a loaded position, the piston rod being further adapted to engage a piston and to be moved proximally towards its loaded position when a cartridge is arranged in a loaded position. The cartridge for which the device is designed may be a conventional drug-filled glass cartridge comprising a cylindrical main portion in which the piston is arranged, and a distal neck portion having an outlet closed by a needle penetrable septum. The distal end may be provided with coupling means for a needle assembly. Alternatively the cartridge may be made from a polymeric material.
By this arrangement the number of actions in connection with a cartridge change can be reduced as it can be ensured (depending on the actual design of the device as discussed below) that the piston rod in all (or most) cases will be in contact with the piston when a new full or partly full cartridge has been loaded (or inserted) into a drug delivery device, this without the user having to manipulate the piston rod which in a front loaded device may be difficult.
Although it can be argued that in most cases when an empty cartridge is replaced with a full cartridge in a device in which the piston rod can be pushed proximally during cartridge change, the piston rod will be positioned in an extended distal position which is then pushed back proximally during cartridge exchange, this ensuring contact between the piston rod and the piston, this is not always the case. Such situations are addressed by the present invention.
For example, if a 75% full cartridge is replaced with a 50% full cartridge the piston rod will not automatically engage the piston of the new cartridge, this resulting in an air gap which could be considerable and would result in severe under-dosing if it was not specified in the device user manual that the user always at cartridge change has to ensure that there is no gap between the piston rod and the piston of a newly inserted cartridge. By providing a drug delivery device in which the piston rod is moved to a loading position corresponding to its distal-most position (or close thereto) when a cartridge is removed, it is assured that the piston rod will engage the piston in virtually any cartridge, even when almost empty. In contrast, if the piston rod was not forwarded automatically, this would either have to be done prior to the insection of a new cartridge or after the insertion. If done prior to insertion the user would have to either use the dose expelling mechanism to forward the piston, or, in case the piston rod is released from the rest of the dose expelling mechanism when a cartridge is removed from the cartridge holder, manually pull forward the piston rod. The latter may be difficult in a front loaded device in which the piston rod is positioned inside the cartridge holder. In this context it should be mentioned that the pistons fully-forwarded distal position is determined by the design of the drug delivery device. More specifically, in a drug delivery device with no end-of-content feature (e.g. NovoPen® 3) the pistons fully-forwarded distal position is determined by the piston being forced into contact with the distal portion of the cartridge, whereas in a drug delivery device with an end-of-content feature (e.g. NovoPen® 4) the pistons fully-forwarded distal position is determined by the piston rod being moved to its distal-most position determined by an end-of-content mechanism.
Alternatively, the present invention could be focused on the intended “normal” use of the drug delivery device, i.e. a given cartridge is replaced with a new cartridge (or a new cartridge is loaded in the device for the first time). As the dimensions of a typical glass cartridge as well as the initial position of the piston are suspect to some production tolerances, the resulting position of the piston relative to the distal end of the piston rod will vary slightly. Thus, by providing a drug delivery device in which the piston rod is moved to a loading position corresponding to a position just slightly proximally of its loaded position, it can be assured that the piston rod will engage the piston in virtually any new cartridge. Such a design could also be used in the manufacturing process of a pre-filled drug delivery device, see below.
By the above arrangement in which the piston rod is moved to its loading position when a cartridge is removed from a loaded position, it can also be prevented that a spring-driven drive mechanism is left in a condition in which a dose can be set and the piston rod moved forward by the spring against essentially no resistance, this resulting in a very fast movement of the piston rod and further components of the expelling mechanism which then would engage mechanical stop means of the dosing mechanism at much higher speeds than under normal use conditions, which then may result in damage or excess wear of the mechanism. Depending on the design, the piston rod may also be moved to the loading position when no cartridge is loaded, this allowing the piston rod to be positioned in the loading position also when the device is loaded with a cartridge for the first time.
In exemplary embodiments the means for moving the piston rod to its loading position when a cartridge is removed from the device is in the form of biasing means, e.g. a spring acting directly or indirectly on the piston rod. The spring could e.g. be a helical spring or a gas spring. In this way the force for moving the piston rod is provided by the biasing means, this allowing the piston rod to be positioned in the loading position also when the device is supplied to the user and no cartridge has yet been removed from the cartridge holding means.
In alternative embodiments the means for moving the piston rod to its loading position when a cartridge is removed from the device is in the form of releasable coupling means providing a coupling, directly or indirectly, between the cartridge and the piston rod, whereby the piston rod is moved to its distal loading position when a cartridge is removed from the device, the coupling means allowing the cartridge to disengage from the piston rod when the piston rod has been moved to its distal loading position. As appears, in this way the force for moving the piston rod is provided by the user removing a cartridge from the cartridge holding means.
In exemplary embodiments the drug delivery device comprises drug expelling means which can be arranged in an operational state and a cartridge loading state, wherein the operational state allows the piston rod to be moved distally relative to the housing during expelling action (e.g. by rotation), and wherein the cartridge loading state allows the piston rod to move axially relative to the housing, this allowing the piston rod to be moved to its distal loading position when a cartridge is removed from a loaded position, and to be moved proximally towards its loaded position when a cartridge is arranged in a loaded position.
The two states could be controlled by means, e.g. a coupling, controlled by the position of the cartridge, e.g. with the cartridge in a loaded position the expelling means would be set in the operational state and with no cartridge positioned in the loaded position the expelling means would be set in the cartridge loading state. The expelling means could be in the form of a mechanical user-settable or fixed dose mechanism which may be either manually actuated or spring-driven, or an electronically controlled motor driven mechanism. The mechanisms may be in the form of an assembly arranged in the device housing or in the form of an assembly formed integrally with the housing.
In a further aspect of the invention a drug delivery system comprising a drug delivery device and a cartridge is provided, the cartridge comprising an axially displaceable piston having an initial proximal position, a continuously-variable intermediate position, and a fully-forwarded distal position. The cartridge may be a conventional drug-filled glass cartridge comprising a cylindrical main portion in which the piston is arranged, and a distal neck portion having an outlet closed by a needle penetrable septum. The distal end may be provided with coupling means for a needle assembly. Alternatively the cartridge may be made from a polymeric material. The drug delivery device comprises a housing, a holder for receiving and holding a cartridge in a loaded position, the holder having a generally tubular configuration with a distal opening adapted to axially receive the cartridge, and drug expelling means comprising an axially displaceable piston rod adapted to engage the piston of a loaded cartridge, the piston rod being moveable between a proximal loaded position and a distal-most position, a loading position being defined distally of the proximal position, wherein the piston rod, when positioned proximally of the loading position, is moved to its loading position when a cartridge is removed from a loaded position, and wherein the piston rod is adapted to engage a piston and to be moved proximally towards its loaded position when a cartridge is arranged in a loaded position.
As also described above for embodiments of the invention, the device part of the system may be provided with biasing means for moving the piston rod to its loading position when a cartridge is removed from the system or when no cartridge is loaded, or, alternatively, releasable coupling means providing a coupling, directly or indirectly, between the cartridge and the piston rod, whereby the piston rod is moved to its loading position when a cartridge is removed from the system, the coupling means allowing the cartridge to disengage from the piston rod when the piston rod has been moved to its loading position. The drug expelling means may be adapted to be arranged in an operational state and a cartridge loading state, the operational state allowing the piston rod to rotate relative to the housing during expelling action, the cartridge loading state allowing the piston rod to move axially relative to the housing, this allowing the piston rod to be moved to its distal loading position when a cartridge is removed from a loaded position, and to be moved proximally towards its loaded position when a cartridge is arranged in a loaded position. As described above, the states may be controlled by the cartridge.
In a yet further aspect of the invention a drug delivery system comprising a drug delivery device and a cartridge is provided, the cartridge comprising an axially displaceable piston having an initial proximal position. The drug delivery device comprises a housing, a holder for receiving and holding a cartridge in a loaded position, the holder having a generally tubular configuration with a distal opening adapted to axially receive the cartridge, drug expelling means comprising an axially displaceable piston rod adapted to engage the piston of a loaded cartridge, the piston rod being moveable between a proximal loaded position and a distal-most position, a loading position being defined distally of the proximal position. The device further comprises biasing means for moving the piston rod to its loading position, whereby the piston rod can engage the piston and be moved from its loading to its loaded position when a cartridge is loaded. The drug expelling means may be configured to be arranged in a cartridge loading state and an operational state, the operational state allowing the piston rod to be moved distally relative to the housing during expelling action, e.g. by rotation, and the cartridge loading state allowing the piston rod to move axially relative to the housing, this allowing the piston rod to be moved proximally towards its loaded position by the piston when a cartridge is arranged in a loaded position. The states may be controlled by the cartridge when inserted. The cartridge and/or the means for receiving and holding the cartridge in a loaded position may be provided with non-releasable coupling means, this allowing the system to be used for the manufacture of a pre-filled drug delivery device. An advantage of such a system would be that a drug-filled cartridge, which is normally the most expensive part of a pre-filled drug delivery device, could be inserted as the final step of the manufacturing process. Further, as the system is designed to eliminate any air gap between the piston and the piston rod when the cartridge is inserted, less cost-effective methods of adjusting the gap can be dispensed with, e.g. positioning a piston rod washer in contact with the piston and then fuse the washer with the piston rod, e.g. by laser welding.
In a further aspect of the invention a method for attaching a cartridge to a drug delivery system is provided, the method comprising the steps of (i) providing a drug-filled cartridge, (ii) providing a front-loaded cartridge holder adapted to axially receive and hold the cartridge in a loaded position, the cartridge holder comprising a distal opening adapted to receive the cartridge in a proximal direction, (iii) inserting the cartridge in the cartridge holder, and (iv) axially locking the received cartridge in the cartridge holder. Depending on the actual design of the locking means the locking step may take place during the final portion of the insertion step. The method steps may include providing a cartridge and a drug delivery device as disclosed above.
As used herein, the term “drug” is meant to encompass any flowable medicine formulation capable of being passed through a delivery means such as a cannula or hollow needle in a controlled manner, such as a liquid, solution, gel or fine suspension, and containing one or more drug agents. The drug may be a single drug compound or a premixed or co-formulated multiple drug compounds drug agent from a single reservoir. Representative drugs include pharmaceuticals such as peptides (e.g. insulins, insulin containing drugs, GLP-1 containing drugs as well as derivatives thereof), proteins, and hormones, biologically derived or active agents, hormonal and gene based agents, nutritional formulas and other substances in both solid (dispensed) or liquid form. In the description of the exemplary embodiments reference will be made to the use of insulin and GLP-1 containing drugs, this including analogues thereof as well as combinations with one or more other drugs.
In the following the invention will be further described with reference to the drawings, wherein
In the figures like structures are mainly identified by like reference numerals.
When in the following terms such as “upper” and “lower”, “right” and “left”, “horizontal” and “vertical” or similar relative expressions are used, these only refer to the appended figures and not to an actual situation of use. The shown figures are schematic representations for which reason the configuration of the different structures as well as their relative dimensions are intended to serve illustrative purposes only.
Referring to
When using a drug delivery device of the above general type (which may have other form-factors and also be provided with a motorized expelling mechanism), the user is typically recommended to take a subcutaneous injection by performing the following steps: remove the cap to uncover the needle mount, mount a new needle assembly, set a dose amount to be expelled by rotating the dose setting member, when the needle has been inserted subcutaneously actuate the release means for driving or releasing the drug expelling means to expel the set dose, after having withdrawn the needle from the skin remove the needle assembly from the needle mount, and re-attach the cap to cover the needle mount.
Referring to
Different alternatives to provide the desired coupling functionality between the cartridge and the cartridge holder will be described with reference to embodiments of a cartridge holder in combination with a drug-filled cartridge, the figures not showing details in respect of the remaining drug delivery device.
The cartridge holder 650 comprises a body portion on which a rotatable sleeve 651 is arranged. The body portion comprises on the inner distal surface coupling means in the form of a plurality of projections 653 providing a plurality of spaces 655 in which the cartridge projections can seat when the cartridge is inserted axially in the cartridge holder with the sleeve in its “open” rotational position. When the sleeve is rotated to its “closed” position the cartridge projections are locked both axially and rotationally in their seated position.
The above-described embodiments of
To prevent that a given cartridge is mounted in a cartridge holder of a drug delivery device not specifically adapted for the contained drug formulation, a cartridge and a corresponding cartridge holder may be provided with corresponding key structures allowing the cartridge to be mounted in the cartridge holder, but preventing a cartridge with a different key structure to be mounted, the latter being adapted to be mounted in a correspondingly adapted other drug delivery device. The key structures may e.g. be a system of projections and receiving slots or grooves and be adapted to be received by relative axial or rotational movement or a combination thereof. The cartridge key structures may be formed integrally with the coupling member.
In the figures only the piston rod is shown. The expelling mechanism may e.g. be driven manually, by a spring energized during dose setting, by a pre-loaded spring or by electrically driven means. The expelling mechanism is provided with coupling means (not shown) acting directly or indirectly on the piston rod and being actuatable between an operational state in which the piston rod can be moved distally to expel a dose of drug from the cartridge, and a loading state in which the piston rod can be moved proximally by e.g. axial movement when a new cartridge is inserted, the piston of the cartridge engaging and pushing the piston rod proximally. The piston rod coupling means may be operated between its loading and operational state (and vice versa) when e.g. a cartridge is inserted (see e.g. US 2004/0210199 which discloses an example of a coupling in which a driving member rotating the piston rod during expelling of a dose can be de-coupled from the expelling mechanism), when the cartridge locking means is operated or by separate additional user operateable means.
In order to ensure that there is no gap between the piston rod and the piston when a new cartridge has been fully inserted and locked in place, the drug delivery device is provided with additional spring means such that the piston rod automatically is moved to its distal loading position when a cartridge is removed from a loaded position and the piston rod thereby un-locked. More specifically, a helical spring 740 is provided providing a distally directed biasing force on the piston rod, the spring being in a (fully or partly) compressed state when the piston rod as shown in
The embodiment of a drug delivery device 800 shown in
The embodiment of a drug delivery device 900 shown in
The embodiment of a drug delivery device 1000 shown in
The embodiment of a drug delivery device 1100 shown in
The embodiment of a drug delivery device 1200 shown in
The above-described embodiments of a pen-formed drug delivery device are all adapted to receive a cartridge through a distal opening, i.e. they are of a front loaded design. However, the different designs for biasing or moving a piston rod to a distal loading position could also be utilized in combination with a rear-loaded cartridge holder. As an alternative the cartridge could be loaded sideways into a cartridge holder, e.g. as in some drug delivery devices having a “dozer” form factor such as Innovo® from Novo Nordisk.
In the above description of exemplary embodiments, the different structures and means providing the described functionality for the different components have been described to a degree to which the concept of the present invention will be apparent to the skilled reader. The detailed construction and specification for the different components are considered the object of a normal design procedure performed by the skilled person along the lines set out in the present specification.
Number | Date | Country | Kind |
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12152496.1 | Jan 2012 | EP | regional |
12156903.2 | Feb 2012 | EP | regional |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2013/051454 | 1/25/2013 | WO | 00 | 7/22/2014 |
Number | Date | Country | |
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61592078 | Jan 2012 | US | |
61604181 | Feb 2012 | US |