The present disclosure relates to an injection activation prevention system of a medicament delivery device and in particular to a cap assembly of a medicament delivery device that has an injection activation prevention feature.
Today's medicament delivery devices may be complex and involves many different components. The physical features of each component and the way components are assembled together has a direct effect on how these components are going to interact with each other and on the success rate of the medicament delivery device in use.
One such area is the use of a needle cover configured to be movable to activate the power pack within of a medicament delivery device for medicament injection.
However, during transportation the medicament delivery device 10 may be moved by externals various forces from sources such as the movement of the transportation vehicle, waves of the sea, or wind. Such forces may result in an unintended retraction of the needle cover 70 in the proximal direction relative to the main housing 20 which results in an accidental activation of the power pack and medicament ejection through the needle of the syringe. Thus, there is a need for ensuring that the needle cover is not moved to retract in the proximal direction by any force other than that applied by the user.
In the present disclosure, when the term “distal” is used, this refers to the direction pointing away from the dose delivery site. When the term “distal part/end” is used, this refers to the part/end of the delivery device, or the parts/ends of the members thereof, which under use of the medicament delivery device is/are located furthest away from the dose delivery site. Correspondingly, when the term “proximal” is used, this refers to the direction pointing to the dose delivery site. When the term “proximal part/end” is used, this refers to the part/end of the delivery device, or the parts/ends of the members thereof, which under use of the medicament delivery device is/are located closest to the dose delivery site.
Further, the term “longitudinal”, with or without “axis”, refers to a direction or an axis through the device or components thereof in the direction of the longest extension of the device or the component.
The term “lateral”, with or without “axis”, refers to a direction or an axis through the device or components thereof in the direction of the broadest extension of the device or the component. “Lateral” may also refer to a position to the side of a “longitudinally” elongated body.
In a similar manner, the terms “radial” or “transversal”, with or without “axis”, refers to a direction or an axis through the device or components thereof in a direction generally perpendicular to the longitudinal direction, e.g. “radially outward” would refer to a direction pointing away from the longitudinal axis.
Also, if nothing else is stated, in the following description wherein the mechanical structure of the device and the mechanical interconnection of its components is described, the device is in an initial non-activated or non-operated state.
In view of the foregoing, a general object of the present disclosure is to provide a needle shield remover for a cap of a medicament delivery device, which needle shield remover is easier to assemble.
These and other aspects of, and advantages with, the present disclosure will become apparent from the following detailed description of the invention and from the accompanying drawings.
According to a main aspect of the disclosure it is characterized by a cap assembly for a medicament delivery device, wherein the medicament delivery device has a housing and a needle cover movable in relation to the housing. The cap assembly comprises a locking member including a flexible first engagement member configured to interact with the needle cover and the housing to limit a movement of the needle cover toward an inside of the housing and a cap configured to engage the locking member and movably arranged in relation to the housing and the locking member between a first position in which the cap is engaged to the housing and a second position in which the cap disengages the housing. One end of the housing is configured to engage the first engagement member to prevent the first engagement member from disengaging the needle cover when the cap is located between the first and second positions. The cap is further movably arranged between the second position and a third position in which the cap disengages the housing and in which the locking member disengages the needle cover and no longer limits the movement of the needle cover.
Further, the needle cover includes a second engagement member configured to engage the first engagement member when the cap is between the first position and the second position, wherein the first engagement member disengages the second engagement member when the cap is moved from the second position to the third position.
The cap assembly also comprises a needle shield remover configured to engage the locking member and a needle shield attached to a medicament container within the needle cover and the housing, when the cap is moved from the second position to the third position the cap moves the locking member to move the needle shield remover away from the medicament container to pull the needle shield away from the medicament container.
The cap includes a third engagement member and the locking member includes a fourth engagement member, the third engagement member is configured to engage the fourth engagement member when the cap moves from the first position to the second position, the third engagement member moves the locking member away from the housing when the cap moves from the second position to the third position.
The cap includes a plurality of gripping protrusions on an outer surface of the cap configured to interact with a user when the user grips the cap.
According to another main aspect of the disclosure it is characterized by a medicament delivery device comprising a housing, a needle cover movably placed at least partially in the housing, a medicament container disposed within the needle cover and the housing, and the cap assembly as described above.
In one embodiment, the housing includes a fifth engagement member on an outer surface of the housing, the cap includes at least a sixth engagement member on an inner surface of the cap, the sixth engagement member is configured to engage the fifth engagement member in order for the cap to be mounted to the housing.
In the following detailed description of the invention, reference will be made to the accompanying drawings, of which
As illustrated in
The needle shield remover 50 is configured to be coupled with the cap 30 so that later the user can pull both the cap 30 and needle shield remover 50 away from housing 20. The needle shield remover 50 is also configured to engage a needle shield attached to the medicament container to cover and protect the needle of the medicament container. More specifically, the needle shield remover 50 includes a plurality of prongs 51 configured to engage the outer surface of the needle shield so that when the cap 40 is pulled by the user the associated needle shield remover 50 can also pull the needle shield off the medicament container.
The locking member 60 is configured to engage the needle cover 70 when the whole cap assembly 30 is coupled with the housing 20 to cover both the proximal portion of the housing 20 and the needle cover 70. More specifically, the locking member 60 includes at least one engagement member 61 configured to engage the needle cover 70 to limit the movement of the needle cover 70 toward the inside of the housing 20 and prevent accidental activation of the power pack when the cap assembly 30 is still attached to the housing 20. As described above, the needle cover 70 retracted into the housing 20 will activate the power pack for the subsequent medicament injection. Thus, by preventing the needle cover 70 from accidental retraction, the locking member 60 and its engagement member 61 also prevent the accident activation of the power pack before the cap assembly 30 is removed from the housing 20. The interaction between the cap assembly 30 and needle cover 70 will be further explained in the later sections.
In the present embodiment, the locking member 60 is disposed between the cap 30 and needle cover 70. The needle cover 70 includes a groove 71 formed on its outer surface. On the other hand, the locking member 60 includes the engagement member 61 extending in a substantially distal direction and is configured to interact with the groove 71. The locking member 60 further includes a stop cam 62 disposed at the end of the engagement member 61 and resting within the groove 71. As described above, the needle cover 70 can be moved in a distal direction back into the housing 20 to activate the power pack (not illustrated) which then drives the syringe 80 in a proximal direction and the medicament out of the syringe 80 through the needle 82. Because the stop cam 62 is located within the groove 71, the needle cover 70 moving in the distal direction will collide with the stop cam 62 and is then prevented from moving further in the distal direction.
However, there is a possibility that excessive force may force the needle cover 70 to bias the engagement member 61 radially outward and then activate the power pack. To prevent such scenario, the end of the engagement member 61 is fitted into the space between the needle cover 70 and the proximal end of the housing 20. In this way, the proximal end of the housing 20 will absorb the force applied on stop arm 61 and thus prevent the engagement member 61 from flexing radially outward. In the present embodiment, the end of the engagement member 61 and the proximal end of the housing 20 have corresponding inclined surface. This allows the end of the engagement member 61 to be fitted into the space between the needle cover 70 and the proximal end of the housing 20.
Also, the stop cam 62 is no longer located within the groove 71 on the needle cover 70. As described above, the locking member 60 is coupled with both the cap 40 and the needle shield remover 50 to form the cap assembly 30. This allows the locking member 60 to move together with the cap 40 when pulled by the user. As the cap 40 is pulled by the user away from the housing 20, the locking member 60 and its stop cam 62 travels along the outer surface of the needle cover 70 and then leaves the groove 71. At this moment, there is nothing to stops the needle cover 70 from moving in a distal direction into the housing 20 to activate the power pack within. Thus, the user should only remove the cap assembly 30 when he/she is ready to use the medicament delivery device 10 for medicament injection. However, if the user changes mind and decides not the initiate the needle penetration and subsequent injector, the user can still couple the cap assembly 30 with the housing 20 to place the stop cam 62 back into the groove 71.
As mentioned above, the needle shield remover 50 is coupled with both the cap 40 and the locking member 60. Thus, when the cap 40 is pulled away from the housing 20, the gripping members 51 of the needle shield remover 50 engages the RNS 84 which engages the FNS 83. Thus, pulling the cap 40 will result in the removal of the FNS 83 and the RNS 84 away from the syringe 80 to expose the needle 82 on the syringe 80.
In the Figures, various engagement features for are shown for providing an engagement between one or more components of the drug delivery device. The engagement features may be any suitable connecting mechanism such as a snap lock, a snap fit, form fit, a bayonet, lure lock, threads or combination of these designs. Other designs are possible as well.
It should be understood that the illustrated components are intended as an example only. In other example embodiments, fewer components, additional components, and/or alternative components are possible as well. Further, it should be understood that the above described and shown embodiments of the present disclosure are to be regarded as non-limiting examples and that they can be modified within the scope of the claims.
While various aspects and embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope being indicated by the following claims, along with the full scope of equivalents to which such claims are entitled. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.
Number | Date | Country | Kind |
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18212091.5 | Dec 2018 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2019/081897 | 11/20/2019 | WO | 00 |