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公开(公告)号:US11944717B2
公开(公告)日:2024-04-02
申请号:US17477947
申请日:2021-09-17
Applicant: Tulavi Therapeutics, Inc. , Incept, LLC
Inventor: Corinne Bright , Yong Ren , Kenneth M. Martin , Farhad Khosravi , Amarpreet S. Sawhney
IPC: A61B17/11 , A61B17/00 , A61F2/00 , A61F2/02 , A61K9/00 , A61L27/18 , A61L27/26 , A61L27/52 , A61L31/14
CPC classification number: A61L27/26 , A61B17/1128 , A61F2/00 , A61F2/02 , A61K9/0004 , A61L27/18 , A61L27/52 , A61L31/14 , A61B2017/00526 , A61F2210/00 , A61F2210/008 , A61F2240/00 , A61F2240/001 , A61F2250/00 , A61L2400/06 , A61L2430/32
Abstract: Disclosed are methods, devices and materials for the in situ formation of a nerve cap and/or a nerve wrap to inhibit neuroma formation following planned or traumatic nerve injury. The method includes the steps of identifying a severed end of a nerve, and positioning the severed end into a cavity defined by a form. A transformable media is introduced into the form cavity to surround the severed end. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the severed end. The media may be a hydrogel, and the transformation may produce a synthetic crosslinked hydrogel protective barrier. The media may include at least one anti-regeneration agent to inhibit nerve regrowth.
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公开(公告)号:US20210361292A1
公开(公告)日:2021-11-25
申请号:US17388327
申请日:2021-07-29
Applicant: Tulavi Therapeutics, Inc. , INCEPT, LLC
Inventor: Corinne Bright , Yong Ren , Ken Martin , Farhad Khosravi , Amarpreet S. Sawhney
Abstract: Disclosed are methods, devices and materials for the in situ formation of an implant for treating a nerve. A treatment site on a nerve is positioned within a cavity defined by a form. A transformable media is introduced into the form cavity to surround the treatment site. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the treatment site. The implant may be a growth inhibiting nerve cap to inhibit neuroma formation following planned or traumatic nerve injury, a growth permissive conduit for facilitating reconnection of a severed nerve, or an anchor for stabilizing a pain management electrode with respect to a nerve. Access to the nerve treatment site may be open surgical or percutaneous.
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公开(公告)号:US11890393B2
公开(公告)日:2024-02-06
申请号:US17138703
申请日:2020-12-30
Applicant: Tulavi Therapeutics, Inc. , Incept, LLC
Inventor: Corinne Bright , Yong Ren , Kenneth M. Martin , Farhad Khosravi , Amarpreet S. Sawhney
IPC: A61B17/11 , A61F2/00 , A61F2/02 , A61K9/00 , A61L27/52 , A61L31/14 , A61B17/00 , A61L27/26 , A61L27/18
CPC classification number: A61L27/26 , A61B17/1128 , A61F2/00 , A61F2/02 , A61K9/0004 , A61L27/18 , A61L27/52 , A61L31/14 , A61B2017/00526 , A61F2210/00 , A61F2210/008 , A61F2240/00 , A61F2240/001 , A61F2250/00 , A61L2400/06 , A61L2430/32
Abstract: Disclosed are methods, devices and materials for the in situ formation of a nerve cap to inhibit neuroma formation following planned or traumatic nerve injury. The method includes the steps of identifying a severed end of a nerve, and positioning the severed end into a cavity defined by a form. A transformable media is introduced into the form cavity to surround the severed end. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the severed end. The media may be a hydrogel, and the transformation may produce a synthetic crosslinked hydrogel protective barrier. The media may include at least one anti-regeneration agent to inhibit nerve regrowth.
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公开(公告)号:US20220054705A1
公开(公告)日:2022-02-24
申请号:US17477947
申请日:2021-09-17
Applicant: Tulavi Therapeutics, Inc. , Incept, LLC
Inventor: Corinne Bright , Yong Ren , Kenneth M. Martin , Farhad Khosravi , Amarpreet S. Sawhney
Abstract: Disclosed are methods, devices and materials for the in situ formation of a nerve cap and/or a nerve wrap to inhibit neuroma formation following planned or traumatic nerve injury. The method includes the steps of identifying a severed end of a nerve, and positioning the severed end into a cavity defined by a form. A transformable media is introduced into the form cavity to surround the severed end. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the severed end. The media may be a hydrogel, and the transformation may produce a synthetic crosslinked hydrogel protective barrier. The media may include at least one anti-regeneration agent to inhibit nerve regrowth
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公开(公告)号:US12096941B2
公开(公告)日:2024-09-24
申请号:US17388327
申请日:2021-07-29
Applicant: Tulavi Therapeutics, Inc. , INCEPT, LLC
Inventor: Corinne Bright , Yong Ren , Ken Martin , Farhad Khosravi , Amarpreet S. Sawhney
CPC classification number: A61B17/12181 , A61F2/0059 , A61F2/02 , A61F2/08 , A61L27/52
Abstract: Disclosed are methods, devices and materials for the in situ formation of an implant for treating a nerve. A treatment site on a nerve is positioned within a cavity defined by a form. A transformable media is introduced into the form cavity to surround the treatment site. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the treatment site. The implant may be a growth inhibiting nerve cap to inhibit neuroma formation following planned or traumatic nerve injury, a growth permissive conduit for facilitating reconnection of a severed nerve, or an anchor for stabilizing a pain management electrode with respect to a nerve. Access to the nerve treatment site may be open surgical or percutaneous.
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公开(公告)号:US20220096711A1
公开(公告)日:2022-03-31
申请号:US17547583
申请日:2021-12-10
Applicant: Tulavi Therapeutics, Inc. , Incept, LLC
Inventor: Corinne Bright , Yong Ren , Kenneth M. Martin , Farhad Khosravi , Amarpreet S. Sawhney
Abstract: Disclosed are methods, devices and materials for the in situ formation of a nerve cap and/or a nerve wrap to inhibit neuroma formation following planned or traumatic nerve injury. The method includes the steps of identifying a severed end of a nerve, and positioning the severed end into a cavity defined by a form. A transformable media is introduced into the form cavity to surround the severed end. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the severed end. The media may be a hydrogel, and the transformation may produce a synthetic crosslinked hydrogel protective barrier. The media may include at least one anti-regeneration agent to inhibit nerve regrowth
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公开(公告)号:US20210315587A1
公开(公告)日:2021-10-14
申请号:US17148427
申请日:2021-01-13
Applicant: Tulavi Therapeutics, Inc. , INCEPT, LLC
Inventor: Corinne Bright , Yong Ren , Ken Martin , Farhad Khosravi , Amarpreet S. Sawhney
Abstract: Disclosed are methods, devices and materials for the in situ formation of an implant for treating a nerve. A treatment site on a nerve is positioned within a cavity defined by a form. A transformable media is introduced into the form cavity to surround the treatment site. The media is permitted to undergo a transformation from a first, relatively flowable state to a second, relatively non flowable state to form a protective barrier surrounding the treatment site. A hydrophilic characteristic of the media cooperates with a hydrophobic characteristic of the surface of the cavity to facilitate a rapid release of the implant from the cavity following the transformation. The implant may be a growth inhibiting nerve cap to inhibit neuroma formation following planned or traumatic nerve injury, a growth permissive conduit for facilitating reconnection of a severed nerve, or an anchor for stabilizing a pain management electrode with respect to a nerve. Access to the nerve treatment site may be open surgical or percutaneous.
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公开(公告)号:US12171869B2
公开(公告)日:2024-12-24
申请号:US15714633
申请日:2017-09-25
Applicant: Incept, LLC.
Inventor: Amarpreet S. Sawhney , Arthur Driscoll , Charles D. Blizzard , Ankita D. Desai , Peter Jarrett
Abstract: Methods of treating an eye for an ocular condition such as placing a composite depot comprising a xerogel with embedded degradable particles into an anterior chamber of an eye to deliver a therapeutic agent. The xerogel is a hydrogel after exposure to intraocular fluid and is degradable. The degradable particles comprise the therapeutic agent and hydrolytically degrade in the anterior chamber to provide a controlled release of the therapeutic agent into the eye. Materials and processes for making depots are provided as well as alternative methods of their use.
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公开(公告)号:US20220370419A1
公开(公告)日:2022-11-24
申请号:US17830968
申请日:2022-06-02
Applicant: Incept, LLC
Inventor: Peter Jarrett , Rami El-Hayek , Timothy S. Jarrett , Charles D. Blizzard , Amarpreet S. Sawhney
IPC: A61K31/436 , A61K31/44 , A61K31/404 , A61K31/502 , A61K31/496 , A61K31/56 , A61K31/517 , A61K31/444 , A61K9/00
Abstract: Drug delivery involving hydrogels as used for various medical conditions, and includes hydrogels formed in an eye with extended drug release times. An embodiment of the invention is a method of delivering a therapeutic agent to a tissue comprising forming a hydrogel in situ in an eye with a therapeutic agent dispersed in the hydrogel, the agent having a low solubility in water. The agent may be essentially insoluble in water. The hydrogel may be made so that 50% to 100% w/w of the agent is released when the hydrogel is from 100% to 50% persistent, with the persistence being a measure of the dry weight of the hydrogel relative to an initial dry weight of the hydrogel.
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公开(公告)号:US11160883B2
公开(公告)日:2021-11-02
申请号:US16817297
申请日:2020-03-12
Applicant: Incept, LLC
Inventor: Patrick Campbell , Amarpreet S. Sawhney
Abstract: Implantable materials visible under ultrasound may be delivered to a selected placement site and biodegrade after a certain period of time. Ultrasound visible implantable materials may be delivered through an applicator and may include ultrasound contrast agents and/or radiopaque agents. Applications include monitoring the delivery of an implant of the implantable materials to the placement site with ultrasound and delivery of therapeutic agents to a tissue at the placement site for treating a patient.
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