EP3727441A1 - Méthodes et appareil pour l'administration de vaccins contre le virus de l'hépatite b (vhb) - Google Patents
Méthodes et appareil pour l'administration de vaccins contre le virus de l'hépatite b (vhb)Info
- Publication number
- EP3727441A1 EP3727441A1 EP18830986.8A EP18830986A EP3727441A1 EP 3727441 A1 EP3727441 A1 EP 3727441A1 EP 18830986 A EP18830986 A EP 18830986A EP 3727441 A1 EP3727441 A1 EP 3727441A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- kit
- hbv
- cartridge
- electrodes
- reservoir
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
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Definitions
- FIGS. 25A-25H show the design and optimization of expression cassettes and DNA plasmids encoding HBV pol and core antigens as described in Example 1;
- FIG. 25A is a schematic representation of an expression strategy in which coding sequences of the HBV core and pol antigens are fused in frame;
- FIG. 25B is a schematic representation of an expression strategy in which coding sequences of both the core and pol antigens are expressed from a single plasmid by means of the ribosomal FA2 slippage site;
- FIG. 25C is a schematic representation of an expression strategy in which the core and pol antigens are expressed from two separate plasmids;
- FIG. 25A is a schematic representation of an expression strategy in which coding sequences of the HBV core and pol antigens are fused in frame;
- FIG. 25B is a schematic representation of an expression strategy in which coding sequences of both the core and pol antigens are expressed from a single plasmid by means of the
- the disclosure provides an apparatus for the delivery of an HBV vaccine to a predetermined site within a subject, comprising a cartridge assembly comprising an outer cartridge, an inner cartridge, a reservoir containing the HBV vaccine, wherein a reservoir containment volume is contained within the outer cartridge and configured to receive the reservoir; an applicator comprising a cartridge assembly receiving volume, a needle hub, and an insertion detector, wherein the insertion detector senses loading of the reservoir in the reservoir containment volume; at least one interlock, wherein the interlock facilitates proper execution of the HBV vaccine administration procedure; at least one injection orifice through which the HBV vaccine is administered; a plurality of penetrating electrodes arranged with a predetermined spatial relationship relative to the orifice; an electrical field generator for generating an electrical signal operatively connected to the electrodes; and a controlled source of energy sufficient to transfer a predetermined amount of the HBV vaccine at a predetermined rate from the reservoir through the orifice to the predetermined site within the subject.
- first nucleic acid molecule and the second nucleic acid molecule are present in the same nucleic acid molecule or in two different nucleic acid molecules.
- EMTAD This objective is accomplished by controlling the spatial and temporal administration of an HBV vaccine relative to application of electrical signals.
- EMTAD is initiated by HBV vaccine injection using a conventional needle-syringe. After the agent has been administered, a device suitable for ESA is applied to the subject at a designated location.
- an HBV core antigen useful for the application is a consensus antigen, preferably a consensus antigen derived from HBV genotypes B, C, and D, more preferably a truncated consensus antigen derived from HBV genotypes B, C, and D.
- the term“protective immunity” or“protective immune response” means that the vaccinated subject is able to control an infection with the pathogenic agent against which the vaccination was done. Usually, the subject having developed a“protective immune response” develops only mild to moderate clinical symptoms or no symptoms at all. Usually, a subject having a“protective immune response” or“protective immunity” against a certain agent will not die as a result of the infection with said agent.
- An immunogenically effective amount can vary depending upon a variety of factors, such as the physical condition of the subject, age, weight, health, etc.; the particular application, e.g., providing protective immunity or therapeutic immunity; and the particular disease, e.g., viral infection, for which immunity is desired.
- An immunogenically effective amount can readily be determined by one of ordinary skill in the art in view of the disclosure.
- CTAA CTAA
- ESA ESA-like styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-styrene-s.
- apparatus or kits suitable for CTAA including for instance apparatus comprising at least one of automatic injection devices and jet injectors.
- the cartridge assembly 100 includes an outer cartridge 102, in some cases termed a housing.
- the outer cartridge 102 is terminated at a distal end by an outer cartridge cap 106.
- the outer cartridge 102 includes an inner cartridge containment volume 150, for receiving an inner cartridge 103, which is received and moves in a slidable manner in relationship to the outer cartridge 102.
- the inner cartridge 103 includes a reservoir containment volume 142 in which the reservoir 101 can be situated.
- the inner cartridge 103 engages with an inner cartridge cap 104 at a distal end.
- the inner cartridge cap 104 has a number of functions, including to lock electrodes 122 in place (the inner cartridge 103 itself has seams that the electrodes 122 are placed into) and to provide a bearing surface for a stick shield 134.
- the inner cartridge cap 104 locks onto the inner cartridge 103.
- the cartridge assembly 100 is inserted into a cartridge assembly receiving volume 403 within the applicator 400. While various ways can be employed to perform this insertion, one way that has been found particularly useful is by way of a pinion gear assembly 448 engaging racks 154 on the outer cartridge 102.
- the desired depth electrode deployment and/or agent administration is affirmatively selected by the physician or other medicament administrator and the same transmitted to the applicator 400.
- the depth can be selected by depth selection buttons 409 (or other equivalent interface such as a toggle switch or sliding switch) and the result displayed on injection depth selection indicators 408 (or, again, other equivalent interface).
- the available injection depths are conveyed to the user by appropriate labeling of the applicator 400 and/or the cartridge 100. In some embodiments, any labeling regarding the injection depth is located on the cartridge 100 and remains visible to the user following installation in the applicator 400. For example, the available injection depths can be labeled on the upper surface of the alignment guide / splay shield 108.
- One or more interlocks can be in place which must be deactivated before the insertion mechanism gear drive ring 478 is caused to rotate, rotating retaining posts 488 into the channels.
- the alignment guide / splay shield 108 by testing for continuity between one or more pads 162 and one or more respective pads 164, it can be determined how far backward or proximal the alignment guide / splay shield 108 has been moved by applied force, and thus if sufficient force exists for proper delivery.
- the state of the circuit is read by the applicator 400 using sensor contacts 434 (see FIG. 16). If sufficient force is indicated, the force contact interlock is deactivated, allowing the user to operate the device.
- the injection drive mechanism 456 include appropriate sensor and control features to determine the position of the injection drive plunger 484 at the time the injection stroke was halted due to the detection of a fault condition or other circumstance in which halting the injection stroke is necessary. Preferably this is achieved through monitoring of the revolution count of the motor used to drive the injection drive plunger 484, but other methods for monitoring the position of the injection drive plunger 484 including optical or electrical sensors can be employed.
- An embodiment of the disclosure involves the use of a planar support structure 124 positioned perpendicularly relative to the elongate orientation of the electrodes.
- the planar support structure is configured with one or more apertures 192 which correspond to the positions of said electrodes in their specified spatial relationship.
- the size, shape, and position of the apertures are configured to allow the support structure to slide smoothly along the elongate length of the electrodes within the array while constraining unwanted motion perpendicular to the direction of electrode deployment.
- the coding sequences of consensus HBV core and pol antigens according to each of the above three expression strategies were cloned into the commercially available expression plasmid pcDNA3.
- pcDNA3 The coding sequences of consensus HBV core and pol antigens according to each of the above three expression strategies were cloned into the commercially available expression plasmid pcDNA3.
- l. HEK-293T cells were transfected with the vectors and protein expression was evaluated by Western blot using a HBV core-specific antigen.
- WPRE Woodchuck HBV post-transcriptional regulatory element
- intron/exon sequence derived from human apolipoprotein Al precursor GenBank: X01038.1
- HTLV-l human T-cell leukemia virus type 1
- LTR long terminal repeat
- composite sequence of the HTLV-l LTR, synthetic rabbit b-globin intron GenBank: V00882.1
- splicing enhancer triple composite sequence
- the device aborts the administration procedure and illuminates the procedure fault indicator.
- the stimulator display of the device provides further instructions.
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Abstract
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201762607430P | 2017-12-19 | 2017-12-19 | |
US2017067269 | 2017-12-19 | ||
PCT/US2018/066157 WO2019126120A1 (fr) | 2017-12-19 | 2018-12-18 | Méthodes et appareil pour l'administration de vaccins contre le virus de l'hépatite b (vhb) |
Publications (1)
Publication Number | Publication Date |
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EP3727441A1 true EP3727441A1 (fr) | 2020-10-28 |
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EP18830986.8A Withdrawn EP3727441A1 (fr) | 2017-12-19 | 2018-12-18 | Méthodes et appareil pour l'administration de vaccins contre le virus de l'hépatite b (vhb) |
Country Status (12)
Country | Link |
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EP (1) | EP3727441A1 (fr) |
JP (1) | JP2021506431A (fr) |
KR (1) | KR20200101388A (fr) |
CN (1) | CN111867624A (fr) |
AU (1) | AU2018390825A1 (fr) |
BR (1) | BR112020012171A2 (fr) |
CA (1) | CA3085492A1 (fr) |
IL (1) | IL275429A (fr) |
MA (1) | MA51292A (fr) |
MX (1) | MX2020006478A (fr) |
SG (1) | SG11202005709QA (fr) |
WO (1) | WO2019126120A1 (fr) |
Families Citing this family (6)
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EA202091516A1 (ru) | 2017-12-19 | 2020-11-03 | Янссен Сайенсиз Айрлэнд Анлимитед Компани | Способы и композиции для индукции иммунного ответа против вируса гепатита b (hbv) |
EA202091513A1 (ru) | 2017-12-19 | 2020-09-09 | Янссен Сайенсиз Айрлэнд Анлимитед Компани | Вакцины против вируса гепатита b (hbv) и их применение |
US11389531B2 (en) | 2017-12-19 | 2022-07-19 | Janssen Sciences Ireland Unlimited Company | Methods and apparatus for the delivery of hepatitis B virus (HBV) vaccines |
EP3986458A1 (fr) * | 2019-06-20 | 2022-04-27 | Janssen Sciences Ireland Unlimited Company | Molécules d'arn à auto-réplication pour vaccins contre le virus de l'hépatite b (vhb) et utilisations associées |
CN111267290B (zh) * | 2020-02-25 | 2021-09-21 | 南京六合科技创业投资发展有限公司 | 一种管道保温维护用保温料自动搅拌填充设备 |
WO2023233290A1 (fr) | 2022-05-31 | 2023-12-07 | Janssen Sciences Ireland Unlimited Company | Agents d'arni ciblant pd-l1 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
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US5780036A (en) * | 1991-08-26 | 1998-07-14 | The Scripps Research Institute | Peptides for inducing cytotoxic T lymphocyte responses to hepattis B virus |
US6041252A (en) | 1995-06-07 | 2000-03-21 | Ichor Medical Systems Inc. | Drug delivery system and method |
US5873549A (en) | 1996-09-25 | 1999-02-23 | Mcdonnell Douglas Corporation | Vehicle rotation and control mechanism |
WO2005012502A2 (fr) * | 2003-03-28 | 2005-02-10 | Idm Pharma, Inc. | Procedes d'identification de variants optimaux d'epitopes peptidiques |
SI1729848T1 (sl) * | 2004-03-08 | 2015-08-31 | Ichor Medical Systems Inc. | Izboljšani aparat za električno posredovan dovod terapevtske snovi |
KR100836745B1 (ko) * | 2007-01-31 | 2008-06-10 | (주)두비엘 | Hbv 백신 및 그의 제조 방법 |
CN102851313B (zh) * | 2008-01-28 | 2015-01-28 | 多贝尔有限公司 | 一种乙型肝炎疫苗及其制备工艺 |
KR20120052352A (ko) * | 2009-08-07 | 2012-05-23 | 트랜스진 에스.에이. | Hbv 감염을 치료하는 조성물 |
EA202092990A3 (ru) * | 2011-02-11 | 2021-07-30 | Дзе Трастиз Оф Дзе Юниверсити Оф Пенсильвания | Молекула нуклеиновой кислоты, кодирующая коровый белок вируса гепатита в, и вакцина, содержащая указанную молекулу |
CA2827150C (fr) * | 2011-02-12 | 2018-09-11 | Globeimmune, Inc. | Therapeutique a base de levure pour infection chronique par l'hepatite b |
TWI575070B (zh) * | 2011-07-12 | 2017-03-21 | 傳斯堅公司 | Hbv聚合酶突變體 |
GB201223386D0 (en) * | 2012-12-24 | 2013-02-06 | Immune Targeting Systems Its Ltd | Vaccine |
WO2016020538A1 (fr) * | 2014-08-08 | 2016-02-11 | Transgene Sa | Traitement en association d'un vaccin contre le hbv et d'un anticorps pour traiter des infections à hbv. |
CA2962799A1 (fr) * | 2014-10-01 | 2016-04-07 | The Trustees Of The University Of Pennsylvania | Vaccins possedant un antigene et une interleukine-21 en tant qu'adjuvant |
CA3018223A1 (fr) * | 2016-03-28 | 2017-10-05 | Ichor Medical Systems, Inc. | Procede et appareil permettant d'administrer des agents therapeutiques |
-
2018
- 2018-12-18 MA MA051292A patent/MA51292A/fr unknown
- 2018-12-18 AU AU2018390825A patent/AU2018390825A1/en not_active Abandoned
- 2018-12-18 CN CN201880089692.8A patent/CN111867624A/zh active Pending
- 2018-12-18 SG SG11202005709QA patent/SG11202005709QA/en unknown
- 2018-12-18 WO PCT/US2018/066157 patent/WO2019126120A1/fr unknown
- 2018-12-18 JP JP2020533179A patent/JP2021506431A/ja active Pending
- 2018-12-18 BR BR112020012171-1A patent/BR112020012171A2/pt unknown
- 2018-12-18 CA CA3085492A patent/CA3085492A1/fr active Pending
- 2018-12-18 KR KR1020207020181A patent/KR20200101388A/ko not_active Application Discontinuation
- 2018-12-18 MX MX2020006478A patent/MX2020006478A/es unknown
- 2018-12-18 EP EP18830986.8A patent/EP3727441A1/fr not_active Withdrawn
-
2020
- 2020-06-17 IL IL275429A patent/IL275429A/en unknown
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JP2021506431A (ja) | 2021-02-22 |
SG11202005709QA (en) | 2020-07-29 |
WO2019126120A1 (fr) | 2019-06-27 |
MX2020006478A (es) | 2020-09-22 |
AU2018390825A1 (en) | 2020-06-18 |
CN111867624A (zh) | 2020-10-30 |
IL275429A (en) | 2020-08-31 |
KR20200101388A (ko) | 2020-08-27 |
MA51292A (fr) | 2020-10-28 |
CA3085492A1 (fr) | 2019-06-27 |
BR112020012171A2 (pt) | 2020-11-24 |
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