Clicker Arrangement and Drug Delivery Device Herewith
20170312438 · 2017-11-02
Inventors
- William Geoffrey Arthur Marsh (Buckinghamshire, GB)
- Matthew Meredith Jones (Warwick Warwickshire, GB)
Cpc classification
A61M5/3157
HUMAN NECESSITIES
A61M5/2033
HUMAN NECESSITIES
A61M5/31583
HUMAN NECESSITIES
A61M5/28
HUMAN NECESSITIES
A61M5/31536
HUMAN NECESSITIES
A61M5/31591
HUMAN NECESSITIES
A61M2005/31518
HUMAN NECESSITIES
A61M5/24
HUMAN NECESSITIES
International classification
A61M5/315
HUMAN NECESSITIES
A61M5/20
HUMAN NECESSITIES
Abstract
The present disclosure is generally directed to a clicker arrangement for use in a drug delivery device, i.e. a handheld injection device for selecting and dispensing a number of user variable doses of a medicament. The clicker arrangement comprises a first element rotatable at least in a first direction and a second, non-rotatable element. The first element is axially displaceable relative to the second element between a first position and a second position. One of the elements comprises a clicker arm and the other comprises a protrusion wherein upon rotation of the first element in the first direction relative to the second element the clicker arm is elastically deflectable in a radial direction by the protrusion and relaxable in the opposite radial direction upon disengagement with the protrusion thereby generating an audible and/or tactile feedback signal.
Claims
1-15. (canceled)
16. A clicker arrangement for use in a drug delivery device, the arrangement comprising: a first element rotatable at least in a first direction; and a second, non-rotatable element, wherein the first element is axially displaceable relative to the second element between a first position and a second position, wherein one of the first element or the second element comprises a clicker arm and the other of the first element or the second element comprises a protrusion, and wherein upon rotation of the first element in the first direction relative to the second element, the clicker arm is elastically deflectable in a radial direction by the protrusion and relaxable in the opposite radial direction upon disengagement with the protrusion, thereby generating an audible or tactile feedback signal, wherein the first element is axially guided on the second element during the rotation of the first element in the first direction relative to the second element, such that the relative rotation is a rotation without concurrent relative axial movement.
17. The clicker arrangement according to claim 16, wherein the first element comprises the clicker arm and the second element comprises the protrusion in the form of a ramp located radially outwards or inwards of the clicker arm.
18. The clicker arrangement according to claim 16, wherein the first element is axially movable relative to the second element between a first position in which the clicker arm and the protrusion (37) do not interfere, and a second position in which the clicker arm is elastically deflectable in a radial direction by the protrusion.
19. The clicker arrangement according to claim 16, wherein the first element has a disc-shaped or cup-shaped form and the second element has a disc-shaped or cup-shaped form, wherein a further element is axially interposed between the first and second element.
20. The clicker arrangement according to claim 16, further comprising a compression spring biasing the first element in its first axial position relative to the second element.
21. A drug delivery device comprising: a clicker arrangement for use in the drug delivery device, the arrangement comprising: a first element rotatable at least in a first direction; and a second, non-rotatable element, wherein the first element is axially displaceable relative to the second element between a first position and a second position, wherein one of the first element or the second element comprises a clicker arm and the other of the first element or the second element comprises a protrusion, and wherein upon rotation of the first element in the first direction relative to the second element, the clicker arm is elastically deflectable in a radial direction by the protrusion and relaxable in the opposite radial direction upon disengagement with the protrusion, thereby generating an audible or tactile feedback signal, wherein the first element is axially guided on the second element during the rotation of the first element in the first direction relative to the second element, such that the relative rotation is a rotation without concurrent relative axial movement, wherein the first element is a coupling element interposed between a dose setting member for setting user variable doses of a medicament and a drive gear which is in meshed engagement with a toothed piston rod, and wherein the second element is a chassis permanently fixed within a housing.
22. The drug delivery device according to claim 21, further comprising a ratchet interface between the coupling element and the drive gear allowing relative rotation between the coupling element and the drive gear during dose setting, wherein the ratchet interface generates a tactile or audible feedback signal upon relative rotation between the coupling element and the drive gear.
23. The drug delivery device according to claim 21, wherein the drive gear rotates relative to the chassis during dose dispensing, the device further comprising a clicker arm provided on the chassis and ratchet teeth provided on the drive gear, wherein the clicker arm and the ratchet teeth generate a tactile or audible feedback signal upon relative rotation between the drive gear and the chassis.
24. The drug delivery device according to claim 21, further comprising a display with a number wheel which is axially constrained within the housing and rotationally constrained to the coupling element.
25. The drug delivery device according to claim 21, wherein the toothed piston rod is in meshed engagement with a pinion of the drive gear and comprises multiple rigid rod pieces which are connected by hinges, and wherein the chassis comprises a first curved guiding section and a second straight guiding section with the pinion of the drive gear being arranged protruding into the second straight guiding section.
26. The drug delivery device according to claim 21, further comprising a clutch provided by a splined portion of the drive gear and a corresponding splined portion of the chassis, wherein the drive gear is axially movable along its rotational axis between a first position in which the drive gear is rotationally constrained to the chassis by engagement of the clutch and a second position in which the clutch is disengaged and relative rotation between the chassis and the drive gear is allowed.
27. The drug delivery device according to claim 21, further comprising a drive spring which is fixed to the chassis with one end and, at least when the drive gear is allowed to rotate relative to the chassis, exerts a force or torque to the drive gear for rotating the drive gear relative to the chassis, which rotation results in a movement of the toothed piston rod.
28. The drug delivery device according to claim 21, wherein the housing has a longitudinal axis defined by a compartment for receiving a cartridge, wherein the dose setting member is arranged rotatable within the housing with its axis of rotation being perpendicular to the longitudinal axis of the housing.
29. The drug delivery device according to claim 21, wherein rotation of the dose setting member, the coupling element and the display is limited by rotational stops defining a minimum dose position and a maximum dose position, wherein the clicker arm disengages from the protrusion thereby generating the audible or tactile feedback signal when the coupling element returns to the minimum dose position at the end of dose dispensing.
30. The drug delivery device according to claim 21, wherein the cartridge contains a medicament.
31. The drug delivery device according to claim 30, wherein the medicament comprises a pharmaceutically active compound.
Description
BRIEF DESCRIPTION OF THE FIGURES
[0065] The present disclosure will now be described in further detail with reference to the accompanying schematic drawings, wherein
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DETAILED DESCRIPTION
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[0090] The casework or body 10 forms together with cartridge holder 20 the housing of the device. It is the basis for relative movements of other component parts during use of the device. Body 10 and cartridge holder 20 may be permanently attached to each other by snap hooks 21. Cartridge holder 20 has an opening into which prism 90 is inserted and permanently fixed. Further, the base element or chassis 30 is permanently attached to the body 10 and cartridge holder 20 such that these component parts behave in use as a single part. The liquid medicament cartridge 140 contains a movable bung 141 and is housed within the cartridge holder 20. Body 10 comprises a protrusion (
[0091] Chassis 30 is a disc-like component with a generally circular configuration. Splines 31 are provided at an inner side for releasably engaging drive gear 110 (
[0092] The trigger or dose button 40 is axially constrained between the dial 50 and dial gear 70. It may be fixed to the dial gear 70 by snap hooks 41. Dose button 40 is axially displaceable relative to the body 10 and to the dial 50.
[0093] The dial 50 is axially constrained to the body 10 via clip features (not shown in
[0094] The last dose nut 60 is located between the dial gear 70 and drive gear 110. It is rotationally coupled to the drive gear 110, via a splined interface (grooves 61 and splines 111). It moves along a helical path relative to the dial gear 70, via a threaded interface (outer thread 62 and inner thread 71), when relative rotation occurs between the dial gear 70 and drive gear 110 (i.e. during dialling). A rotational end stop 63 is provided on the nut 60 for engagement with a last dose stop 72 on dial gear 70 (
[0095] Dial gear 70 is a cup shaped member with an annular recess in its upper surface (in
[0096] The trigger spring 80 applies a force between the chassis 30 and drive gear 110 to separate them. In the “at rest” condition, this ensures that the drive gear 110 is rotationally coupled to the chassis 30 and that the spline teeth 73 of dial gear 70 are engaged with the dial 50 (
[0097] The dose set is displayed on the outer surface of the device to provide feedback to the user. In this embodiment, the prism 90 reflects the display from the number wheel 100 so that the dose is displayed on the front face of the device (
[0098] An alternative embodiment negates the requirement for the prism 90 component and displays the dose on the side of the device. The number wheel 100 is then printed with conventional, non-mirrored, text and a small window is formed in the side of the body 10.
[0099] The number wheel 100 is axially constrained between the chassis 30 and body 10. It is rotationally coupled to the dial gear 70, via a splined interface (splines 75), that permits relative axial movement between the dial gear 70 and number wheel 100. The number wheel 100 is free to rotate, relative to the body 10, between two fixed, rotational stops formed by abutments on the number wheel 100 and body 10. A sequence of numbers, markings or symbols is provided on the outer circumference of the number wheel 100.
[0100] The drive gear 110 is axially constrained between the chassis 30 and dial gear 70 and biased away from the chassis 30 by the trigger spring 80. It is rotationally coupled to the dial gear 70 via a detent and clutch interface (
[0101] The flexible piston rod 120 is located within the chassis 30 and engages, via a rack and pinion interface, the drive gear 110 so that CCW rotation of the drive gear 110 advances the piston rod 120. The distal end of the piston rod 120 acts on the bung 141 within the liquid medicament cartridge 140. As shown in
[0102] The drive spring 130 is attached at one end to the chassis 30 and at the other end to the number wheel 100. The drive spring 130 is pre-wound upon assembly, such that it applies a torque to the number wheel 100 when the mechanism is at zero units dialed. The action of rotating the dial 50, to set a dose, rotates the dial gear 70 and number wheel 100 relative to the chassis 30, and (further) winds up the spring. As shown in
[0103] The drug delivery device can be operated to deliver a number of user variable doses of medicament from the cartridge 140, via a needle (not shown). The device is disposable and is delivered to the user in a fully assembled condition ready for use. The mechanism provides separate user interfaces for setting and delivery of a dose. In short, a dose is set by rotating dial 50 located on the face of the device. Delivery of a dose is initiated by pressing dose button 40, positioned in the center of the dial 50, and dose delivery will continue while the dose button 40 remains depressed, until the complete set dose has been delivered. The mechanism provides audible, visual and tactile feedback both on the setting and delivery of each dose. Any dose size can be selected between zero and a pre-defined maximum, in increments to suit the medicament and user profile. The mechanism permits cancelling of a dose without any medicament being dispensed by rotation of the dial 50 in the opposing direction to when selecting a dose.
[0104] The force required to actuate the dose button 40 and the distance which it has to move are small, providing a significant ergonomic advantage, particularly for those users with impaired dexterity. The mechanism requires consistent user input forces to set a dose and initiate the delivery of a dose, which are insensitive to variations in the force required to displace the bung 141 within the cartridge 140. The dial 50 is disengaged during dose delivery so that it does not rotate which improves handling of the device during use. The device has relatively low part count, very compact size and is particularly attractive for cost sensitive device applications.
[0105] In the following use and function of the device will be described in more detail.
[0106] With the device in the at rest condition, dose marking ‘0’ on the number wheel 100 is visible through the prism 90 in the Body (
[0107] The user selects a variable dose of liquid medicament by rotating the dial 50 CW, which generates an identical rotation in the dial gear 70. Rotation of the dial gear 70 causes rotation of the number wheel 100, which in turn causes wind up of the drive spring 130, increasing the energy stored within it. The drive gear 110 is still prevented from rotating, due to the engagement of its splined teeth 113 with the chassis 30. Relative rotation must therefore occur between the dial gear 70 and drive gear 110, via the detent and clutch interface 74, 112.
[0108] The user torque required to rotate the dial 50 is a sum of the torque required to wind up the drive spring 130, and the torque required to overhaul the ratchet feature 74, 112. The trigger spring 80 acts to provide an axial force to engage the ratchet feature 74, 112 and to bias the components (drive gear 110, dial gear 70 and dose button 40) away from the chassis 30 and towards the dial 50. The axial load acts to maintain the ratchet teeth 74, 112 engagement of the dial gear 70 and drive gear 110. The torque required to overhaul the ratchet 74, 112 is resultant from the axial load applied by the trigger spring 80, the CW ramp angle of the ratchet 74, 112, the friction coefficient between the mating surfaces and the mean radius of the ratchet features.
[0109] As the user rotates the dial 50 sufficiently to increment the mechanism by 1 unit, the dial gear 70 rotates relative to the drive gear 110 by one ratchet tooth 74, 112. At this point the ratchet teeth re-engage into the next detented position. An audible click is generated by the ratchet re-engagement, and tactile feedback is given by the change in torque input required.
[0110] Relative rotation of the dial gear 70 and the drive gear 110 causes the last dose nut 60 to travel axially, via the threaded engagement with the dial gear 70, towards the last dose abutment 72 on the dial gear 70 (
[0111] The selected dose is displayed through the body 10 via the number wheel 100 and prism 90 as described previously. Irrespective of whether the dial 50 is rotated CW or CCW, the dose displayed will always indicate the dose to be dispensed. In addition, the dose display also decrements as the dose is dispensed and thus displays the dose remaining to be dispensed.
[0112] CW rotation of the dial gear 70 rotates the number wheel 100 away from the zero unit stop 11 on the body 10 (
[0113] With no user torque applied to the dial 50, the dial gear 70 is now prevented from rotating under the action of the torque applied by the drive spring 130, solely by the ratchet engagement 74, 112 between the dial gear 70 and the drive gear 110. The torque necessary to overhaul the ratchet in the CCW direction is resultant from the axial load applied by the trigger spring 80, the CCW ramp angle of the ratchet 74, 112, the friction coefficient between the mating surfaces and the mean radius of the ratchet features. The torque necessary to overhaul the ratchet must be greater than the torque applied to the number wheel 100 (and hence dial gear 70) by the drive spring 130. The ratchet ramp angle is therefore increased in the CCW direction to ensure this is the case.
[0114] The user may now choose to increase the selected dose by continuing to rotate the dial 50 in the CW direction. The process of overhauling the detent and clutch interface 74, 112 between the dial gear 70 and drive gear 110 is repeated for each dose unit. Additional energy is stored within the drive spring 130 for each dose unit and audible and tactile feedback is provided for each unit dialed by the re-engagement of the teeth 74, 112. The torque required to rotate the dial 50 increases as the torque required to wind up the drive spring 130 increases. The torque required to overhaul the ratchet in the CCW direction must therefore be greater than the torque applied to the dial gear 70 by the drive spring 130 when the maximum dose has been reached.
[0115] If the user continues to increase the selected dose until the maximum dose limit 12, 101 is reached, the number wheel 100 engages with its maximum dose abutment on the body 10, which prevents further rotation of the number wheel 100, dial gear 70 and dial 50. At this point the maximum dose marking on the number wheel 100 is aligned to the prism 90 and shown on the front of the device. Depending on how many units have already been delivered by the mechanism, during selection of a dose, end stop 63 of the last dose nut 60 may contact its last dose abutment 72 with the dial gear 70 (
[0116] With the mechanism in a state in which a dose has been selected, the user is able to deselect any number of units from this dose. Deselecting a dose is achieved by the user rotating the dial 50 CCW. The torque applied to the dial 50 by the user is sufficient, when combined with the torque applied by the drive spring 130, to overhaul the ratchet 74, 112 between the dial gear 70 and drive gear 110 in the CCW direction. When the ratchet is overhauled, CCW rotation occurs in the number wheel 100 (via the dial gear 70), which returns the number wheel 100 towards the zero dose position, and unwinds the drive spring 130. The relative rotation between the dial gear 70 and drive gear 110 causes the last dose nut 60 to return axially, away from the last dose abutment.
[0117] An alternative embodiment of the dial gear 70 to drive gear 110 interface depicted in
[0118] Cam ring 150 comprises four splines 151 which engage with slots 76 dial gear 70. On its upper side facing towards the dial 50, the cam ring 150 is provided with ramp-like saw teeth 152 engaging corresponding ramp-like saw teeth 52 of the dial. In addition, straight spline features 53 and 153 are provided on the dial 50 and the cam ring 150 (
[0119] During dose set (CW dial rotation) the vertical abutments of ramp-like saw teeth 52 of dial 50 engage with vertical abutments of ramp-like saw teeth 152 of the cam ring 150 to directly transmit torque to the dial gear 70 via the spline engagement (splines 151 and slots 76) between the cam ring 150 and dial gear 70. Rotation of the dial gear 70 causes wind up of the drive spring 130, increasing the energy stored within it. The drive gear 110 is still prevented from rotating, due to the engagement of its splined teeth 113 with the chassis 30. Relative rotation must therefore occur between the dial gear 70 and drive gear 110, via the detent and clutch interface 74′, 112′. The at rest position is shown in
[0120] When the dial 50 is rotated CCW the dial gear 70 and cam ring 150 are not carried by it due to the profile of the detent and clutch interface (saw teeth 74′, 112′) between the dial gear 70 and drive gear 110 (which is rotationally coupled to the chassis 30 throughout the dose select or deselect action). CCW rotation of the dial 50, therefore, results in relative rotation between the cam ring 150 and dial 50. The ramp features of saw teeth 52,152 between dial 50 and cam ring 150 cause the cam ring 150 to displace axially as a result of the relative rotation (
[0121] When the dial 50 has rotated sufficiently to disengage detent and clutch interface 74′, 112′, splines 53 on the dial 50 contact splines 153 on the cam ring 150 and prevent further relative rotation between the dial 50 and cam ring 150. Clearance between the splines 53, 153 allows enough relative rotation of the dial 50 and cam ring 150 to disengage detent and clutch interface 74′, 112′, but not enough for the saw-teeth 52, 152 to override each other and cause the dial 50 to become de-synchronised with the cam ring 150 and dial gear 70.
[0122] Detent and clutch interface (74′, 112′) reacts the drive spring 130 torque, applied to the dial gear 70 via the number wheel 100. When the detent and clutch interface is disengaged, the drive spring 130 torque rotates the dial gear 70 CCW by one unit increment via the number wheel 100 (
[0123] The cam ring 150 is then driven rotationally by the dial gear 70, relative to the dial 50, returning along the helical path and to its original axial position. The trigger spring 80 returns the drive gear 110 axially and re-engages the detent and clutch interface 74′ and 112′ between dial gear 70 and drive gear 110 (
[0124] With any of the above mentioned alternative mechanisms in a state in which a dose has been selected, the user is able to activate the mechanism to commence delivery of a dose. Delivery of a dose is initiated by the user depressing the dose button 40 in the center of the dial 50.
[0125] When the dose button 40 is depressed, it moves axially, acting on the dial gear 70, which in turn acts on the drive gear 110. The dial gear 70 disengages its spline teeth 73 from the dial 50 and then the drive gear 110 disengages its spline teeth 113 from the corresponding teeth 31 of the chassis 30 (
[0126] The torque applied to the dial gear 70, via the number wheel 100, from the drive spring 130 is transmitted, via the detent and clutch interface, into the drive gear 110. This torque causes rotation of the drive gear 110 and hence, due to its geared engagement with the piston rod 120, advancement of the piston rod 120. Axial displacement of the piston rod 120 forces liquid medicament to be delivered from the mechanism, as the distal end of the piston rod 120 contacts and displaces the bung 141 within the cartridge 140. The rotation of the dial gear 70 also causes the number wheel 100 to rotate CCW, towards the zero dose abutment and decrementing the dose displayed.
[0127] The clicker arm 36 is a compliant cantilever beam integrated into the chassis 30, which interfaces axially with ratchet features 115 on the drive gear 110. The ratchet teeth spacing corresponds to the drive gear 110 rotation required to deliver a single dose unit. During dispense, as the drive gear 110 rotates, the ratchet features 115 engage with the clicker arm 36 to produce an audible click with each dose unit delivered (
[0128] Delivery of a dose continues via the mechanical interactions described above while the user continues to depress the dose button 40. If the user releases the dose button 40, the trigger spring 80 returns the dose button 40 to its at rest position via the drive gear 110 and dial gear 70, the drive gear 110 becomes rotationally constrained and delivery of a dose is halted.
[0129] With the dose button 40 depressed, delivery of a dose continues until the number wheel 100 reaches the zero dose abutment 102 with the body 10. The torque applied to the number wheel 100 by the drive spring 130 is reacted by the abutment of the number wheel 100 to the body 10 and the number wheel 100, dial gear 70 and drive gear 110 are prevented from rotating further. During delivery of a dose, the drive gear 110 and dial gear 70 rotate together, so that no relative motion in the last dose nut 60 occurs. The last dose nut 60 therefore travels towards its abutment on the dial gear 70 during dialling only.
[0130] Once the delivery of a dose is stopped, by the number wheel 100 returning to the zero dose abutment 11, the user may release the dose button 40, which will re-engage the chassis 30 spline teeth 31 with teeth 113 of the drive gear 110. The mechanism is now returned to the at rest condition.
[0131] It is possible to angle either the spline teeth 113 on the drive gear 110 or the spline teeth 31 on chassis 30 so that when the dose button 40 is released the re-engagement of the spline teeth 31, 113 fractionally ‘backwind’ the drive gear 110 thereby removing the engagement of the number wheel 100 to the chassis 30 zero dose stop abutment (
[0132] An audible click occurs at the end of dose when the mechanism reaches its zero position 11, 102. The click is created by interaction between ramp 37 of the chassis 30 and a flexible clicker arm 77 on the dial gear 70 when the dial gear 70 is in the dispensing axial position. The advantage with this design is that the click feedback only occurs during dose delivery (
[0133] The sequence of generating the click is shown in
[0134] A further aspect of the present disclosure pertains to the facility for removing the need for a user to prime the device when first used. This involves removing the variable distance (dependent on component and cartridge tolerances) between the bung 141 of cartridge 140 and the distal face (foot 125) of the piston rod 120 during manufacture such that the piston rod 120 is in contact with the bung 141 when assembled. For this prime elimination the device is assembled completely, however omitting the dose button 40. An assembly tool 160 engages with location features 116 in the drive gear 110, through cut-outs 78 in the dial gear 70 (
[0135] As an alternative to the embodiments depicted in the Figures which comprise a prism, a window or opening may be provided in the body, for example in the cylindrical side surface, through which markings of the number wheel 100 are visible.
TABLE-US-00001 Reference numerals 10 body (casework) 11 minimum stop 12 maximum stop 20 cartridge holder 21 snap hook 30 chassis 31 spline teeth 32 bearing 33 first curved guiding section 34 second straight guiding section 35 receiving section 36 clicker arm 37 ramp 40 dose button 41 snap hook 50 dial (dose setting member) 51 dial cover 52 saw teeth 53 spline 60 last dose nut 61 groove 62 outer thread 63 end stop 70 dial gear (coupling element) 71 thread 72 stop 73 teeth 74, 74′ ratchet teeth 75 spline 76 slot 77 clicker arm 78 cut-out 80 trigger spring 90 prism 100 number wheel (display) 101 maximum stop 102 minimum stop 110 drive gear 111 spline 112, 112′ ratchet teeth 113 spline teeth 114 pinion 115 ratchet 116 location feature 120 flexible piston rod 121 segment (rigid rod piece) 122 hinge 123 rack teeth 124 flange 125 foot 130 drive spring (torsion spring) 140 cartridge 141 bung 150 cam ring 151 spline 152 saw teeth 153 spline 160 assembly tool