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Kanji M Meghpara

age ~66

from Morris Plains, NJ

Also known as:
  • Melissa K Meghpara
  • Kenji M Meghpara
  • Kanji M Meghara
  • Meghan Meghpara
Phone and address:
60 Stockton Ct, Greystone Park, NJ 07950
973-829-1872

Kanji Meghpara Phones & Addresses

  • 60 Stockton Ct, Morris Plains, NJ 07950 • 973-829-1872
  • Palo Alto, CA
  • Mountain View, CA
  • Parsippany, NJ
  • Lincoln, NE

Us Patents

  • Compositions With Hydrophilic Drugs In A Hydrophobic Medium

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  • US Patent:
    20060222701, Oct 5, 2006
  • Filed:
    Mar 28, 2006
  • Appl. No.:
    11/391518
  • Inventors:
    Neema Kulkarni - Randolph NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • International Classification:
    A61K 9/48
  • US Classification:
    424451000
  • Abstract:
    In various embodiments of the present invention, a capsule is provided including a hydrophobic inner layer and at least one hydrophilic outer layer. The hydrophobic layer may include a hydrophilic component such as an active pharmaceutical ingredient (API) which may be fully encapsulated, partially encapsulated or part of an adsorption complex. Such capsules experience no or minimal cracking or breaking in the outer layer.
  • Compositions And Capsules With Stable Hydrophilic Layers

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  • US Patent:
    20070134493, Jun 14, 2007
  • Filed:
    Dec 8, 2005
  • Appl. No.:
    11/296989
  • Inventors:
    Kanji Meghpara - Morris Plains NJ, US
  • International Classification:
    B32B 9/00
  • US Classification:
    428402200
  • Abstract:
    Several embodiments of the present invention provide a capsule including a hydrophobic inner core layer and at least one hydrophilic outer layer. The outer layer may be seamless and may include at least one hygroscopic polyol and at least one polyol with a low hygroscopicity. The at least one outer layer may include at least one film or gel forming agent. Such capsules are stable and experience minimal or no degradation under accelerated stability conditions.
  • Sustained Release Paracetamol Formulations

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  • US Patent:
    20140065213, Mar 6, 2014
  • Filed:
    May 4, 2012
  • Appl. No.:
    14/115896
  • Inventors:
    Dongzhou Liu - Parsippany NJ, US
    Kanji Meghpara - Parsippany NJ, US
  • Assignee:
    GlaxoSmithKline, LLC - Philadelphia
  • International Classification:
    A61K 9/24
    A61K 31/167
  • US Classification:
    424472, 514630
  • Abstract:
    The present invention is directed to twice daily sustained release pharmaceutical composition of paracetamol having an immediate release phase of paracetamol and a sustained release phase of paracetamol, said composition having unique and advantageous pharmacokinetic properties and a pharmaceutical composition comprising only a sustained release phase of paracetamol having unique and advantageous pharmacokinetic properties.
  • Self-Regulating Osmotic Gastroretentive Drug Delivery Systems

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  • US Patent:
    20210137827, May 13, 2021
  • Filed:
    Jan 19, 2021
  • Appl. No.:
    17/151782
  • Inventors:
    - Bridgewater NJ, US
    Dipen Desai - Whippany NJ, US
    Wantanee Phuapradit - Montville NJ, US
    Jaydeep Vaghashiya - Franklin park NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • Assignee:
    KASHIV SPECIALTY PHARMACEUTICALS, LLC - Bridgewater NJ
  • International Classification:
    A61K 9/00
    A61K 47/32
    A61K 47/12
    A61K 47/02
  • Abstract:
    Self-regulating, osmotic, floating gastroretentive compositions that provide extended release, delayed release, and/or delayed extended release of active pharmaceutical agents, as well as, optionally, immediate release of the same or a different active pharmaceutical agent, are provided here. The gastroretentive compositions of the disclosure comprise a swellable, extended release, multilayer core comprising a push layer and a pull layer; a water-insoluble permeable elastic membrane surrounding the multilayer core; and an orifice (e.g., a laser-drilled orifice, a manually drilled orifice) on the pull-layer side of the dosage form. The gastric retention of the composition is controlled by rapid floating of the composition and expansion of the membrane. The rapid swelling of the composition to a size greater than the size of the pyloric sphincter is due to the presence of an osmogen, adequate membrane permeability that provides for fast generation of COfrom a gas-generating agent(s), and adequate membrane elasticity that provides for rapid expansion of the membrane. The hydrated core, especially the polyethylene oxide in the push layer, and the permeable elastic membrane with an orifice (1) provide extended release of the active pharmaceutical agent, and (2) maintain the dosage form at a size suitable for gastric retention. The self-regulating composition collapses, or breaks into pieces, after releasing at least about 80% of the drug from the composition.
  • Self-Regulating Osmotic Gastroretentive Drug Delivery Systems

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  • US Patent:
    20210052487, Feb 25, 2021
  • Filed:
    Oct 29, 2020
  • Appl. No.:
    17/083766
  • Inventors:
    - Bridgewater NJ, US
    Dipen Desai - Whippany NJ, US
    Wantanee Phuapradit - Montville NJ, US
    Jaydeep Vaghashiya - Franklin park NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • Assignee:
    KASHIV SPECIALTY PHARMACEUTICALS, LLC - Bridgewater NJ
  • International Classification:
    A61K 9/00
    A61K 47/02
    A61K 47/12
    A61K 47/32
  • Abstract:
    Self-regulating, osmotic, floating gastroretentive compositions that provide extended release, delayed release, and/or delayed extended release of active pharmaceutical agents, as well as, optionally, immediate release of the same or a different active pharmaceutical agent, are provided here. The gastroretentive compositions of the disclosure comprise a swellable, extended release, multilayer core comprising a push layer and a pull layer; a water-insoluble permeable elastic membrane surrounding the multilayer core; and an orifice (e.g., a laser-drilled orifice, a manually drilled orifice) on the pull-layer side of the dosage form. The gastric retention of the composition is controlled by rapid floating of the composition and expansion of the membrane. The rapid swelling of the composition to a size greater than the size of the pyloric sphincter is due to the presence of an osmogen, adequate membrane permeability that provides for fast generation of COfrom a gas-generating agent(s), and adequate membrane elasticity that provides for rapid expansion of the membrane. The hydrated core, especially the polyethylene oxide in the push layer, and the permeable elastic membrane with an orifice (1) provide extended release of the active pharmaceutical agent, and (2) maintain the dosage form at a size suitable for gastric retention. The self-regulating composition collapses, or breaks into pieces, after releasing at least about 80% of the drug from the composition.
  • Self-Regulating Osmotic Gastroretentive Drug Delivery Systems

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  • US Patent:
    20200330368, Oct 22, 2020
  • Filed:
    Jun 29, 2020
  • Appl. No.:
    16/914540
  • Inventors:
    - Bridgewater NJ, US
    Dipen Desai - Whippany NJ, US
    Wantanee Phuapradit - Montville NJ, US
    Jaydeep Vaghashiya - Woodbridge NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • Assignee:
    KASHIV BIOSCIENCES, LLC - Bridgewater NJ
  • International Classification:
    A61K 9/00
    A61K 47/02
    A61K 47/12
    A61K 47/32
  • Abstract:
    Self-regulating, osmotic, floating gastroretentive compositions that provide extended release, delayed release, and/or delayed extended release of active pharmaceutical agents, as well as, optionally, immediate release of the same or a different active pharmaceutical agent, are provided here. The gastroretentive compositions of the disclosure comprise a swellable, extended release, multilayer core comprising a push layer and a pull layer; a water-insoluble permeable elastic membrane surrounding the multilayer core; and an orifice (e.g., a laser-drilled orifice, a manually drilled orifice) on the pull-layer side of the dosage form. The gastric retention of the composition is controlled by rapid floating of the composition and expansion of the membrane. The rapid swelling of the composition to a size greater than the size of the pyloric sphincter is due to the presence of an osmogen, adequate membrane permeability that provides for fast generation of COfrom a gas-generating agent(s), and adequate membrane elasticity that provides for rapid expansion of the membrane. The hydrated core, especially the polyethylene oxide in the push layer, and the permeable elastic membrane with an orifice (1) provide extended release of the active pharmaceutical agent, and (2) maintain the dosage form at a size suitable for gastric retention. The self-regulating composition collapses, or breaks into pieces, after releasing at least about 80% of the drug from the composition.
  • Self-Regulating Osmotic Gastroretentive Drug Delivery Systems

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  • US Patent:
    20200179267, Jun 11, 2020
  • Filed:
    Jan 31, 2020
  • Appl. No.:
    16/778439
  • Inventors:
    - Bridgewater NJ, US
    Wantanee Phuapradit - Montville NJ, US
    Dipen Desai - Whippany NJ, US
    Jaydeep Vaghashiya - Woodbridge NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • Assignee:
    KASHIV BIOSCIENCES, LLC - Bridgewater NJ
  • International Classification:
    A61K 9/00
    A61K 47/02
    A61K 47/12
    A61K 47/32
  • Abstract:
    Self-regulating, osmotic, floating gastroretentive compositions that provide extended release, delayed release, and/or delayed extended release of active pharmaceutical agents, as well as, optionally, immediate release of the same or a different active pharmaceutical agent, are provided here. The gastroretentive compositions of the disclosure comprise a swellable, extended release, multilayer core comprising a push layer and a pull layer; a water-insoluble permeable elastic membrane surrounding the multilayer core; and an orifice (e.g., a laser-drilled orifice, a manually drilled orifice) on the pull-layer side of the dosage form. The gastric retention of the composition is controlled by rapid floating of the composition and expansion of the membrane. The rapid swelling of the composition to a size greater than the size of the pyloric sphincter is due to the presence of an osmogen, adequate membrane permeability that provides for fast generation of COfrom a gas-generating agent(s), and adequate membrane elasticity that provides for rapid expansion of the membrane. The hydrated core, especially the polyethylene oxide in the push layer, and the permeable elastic membrane with an orifice (1) provide extended release of the active pharmaceutical agent, and (2) maintain the dosage form at a size suitable for gastric retention. The self-regulating composition collapses, or breaks into pieces, after releasing at least about 80% of the drug from the composition.
  • Self-Regulating Osmotic Gastroretentive Drug Delivery Systems

    view source
  • US Patent:
    20200155446, May 21, 2020
  • Filed:
    Jun 27, 2019
  • Appl. No.:
    16/634792
  • Inventors:
    - Bridgewater NJ, US
    Wantanee Phuapradit - Montville NJ, US
    Dipen Desai - Whippany NJ, US
    Jaydeep Vaghashiya - Woodbridge NJ, US
    Kanji Meghpara - Morris Plains NJ, US
  • Assignee:
    KASHIV BIOSCIENCES, LLC - Bridgewater NJ
  • International Classification:
    A61K 9/00
    A61K 47/32
    A61K 47/12
    A61K 47/02
  • Abstract:
    Self-regulating, osmotic, floating gastroretentive compositions that provide extended release, delayed release, and/or delayed extended release of active pharmaceutical agents, as well as. optionally, immediate release of the same or a different active pharmaceutical agent, are provided here. The gastroretentive compositions of the disclosure comprise a swellable, extended release, multilayer core comprising a push layer and a pull layer; a water-insoluble permeable elastic membrane surrounding the multilayer core; and an orifice (e.g., a laser-drilled orifice, a manually drilled orifice) on the pull-layer side of the dosage form. The gastric retention of the composition is controlled by rapid floating of the composition and expansion of the membrane. The rapid swelling of the composition to a size greater than the size of the pyloric sphincter is due to the presence of an osmogen. adequate membrane permeability that provides for fast generation of COfrom a gas-generating agent(s), and adequate membrane elasticity that provides for rapid expansion of the membrane. The hydrated core, especially the polyethylene oxide in the push layer, and the permeable elastic membrane with an orifice (1) provide extended release of the active pharmaceutical agent, and (2) maintain the dosage form at a size suitable for gastric retention. The self-regulating composition collapses, or breaks into pieces, after releasing at least about 80% of the drug from the composition.

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