Thomas Kretschmann as Alfredo Grossi; Marco Leonardi as Marco Longhi; Luigi Diberti as Insp. Manetti; Paolo Bonacelli as Dr. Cavanna; Julien Lambroschini as Marie
Us Patents
Stable Solid Formulation Of A Gc-C Receptor Agonist Polypeptide Suitable For Oral Administration
Angelika Fretzen - Somerville MA, US Steven Witowski - Melrose MA, US Alfredo Grossi - Somerville MA, US Hong Zhao - Lexington MA, US Mahendra Dedhiya - Pomona NY, US Yun Mo - Commack NY, US
Assignee:
Ironwood Pharmaceuticals Inc. - Cambridge MA
International Classification:
A61K 38/10 A61P 1/00
US Classification:
514 14
Abstract:
Solid, stable formulations of linaclotide suitable for oral administration are described herein as are methods for preparing such formulations. The formulations described herein contain a polypeptide consisting of the amino acid sequence Cys Cys Glu Tyr Cys Cys Asn Pro Ala Cys Thr Gly Cys Tyr (“linaclotide”) or a pharmaceutically acceptable salt thereof. The linaclotide formulations described herein are stable and have a sufficient shelf life for manufacturing, storing and distributing the drug.
Pharmaceutical Composition And Administration Thereof
William Rowe - Medford MA, US Patricia Hurter - Harvard MA, US Christopher Young - Waltham MA, US Kirk Dinehart - Holliston MA, US Marinus Jacobus Verwijs - Framingham MA, US Kirk Overhoff - Waltham MA, US Peter D.J. Grootenhuis - San Diego CA, US Martyn Botfield - Concord MA, US Alfredo Grossi - Somerville MA, US
The present invention relates to pharmaceutical compositions comprising a solid dispersion of N-[2,4-Bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide, methods of manufacturing pharmaceutical compositions of the present invention, and methods of administering pharmaceutical compositions of the present invention.
Pharmaceutical Composition And Administrations Thereof
William Rowe - Medford MA, US Patricia Hurter - Harvard MA, US Christopher R. Young - Waltham MA, US Kirk Dinehart - Holliston MA, US Marinus Jacobus Verwijs - Framingham MA, US Kirk Overhoff - Waltham MA, US Peter D.J. Grootenhuis - San Diego CA, US Martyn Botfield - Concord MA, US Alfredo Grossi - Somerville MA, US Gregor Zlokarnik - La Jolla CA, US Fredrick F. Van Goor - San Diego CA, US
Assignee:
Vertex Pharmaceuticals Incorporated - Cambridge MA
International Classification:
A61K 31/47 A61P 19/10 A61P 19/08 A61P 11/00
US Classification:
514312
Abstract:
The present invention relates to pharmaceutical compositions comprising a solid dispersion of N-[2,4-Bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide, methods of manufacturing pharmaceutical compositions of the present invention, and methods of administering pharmaceutical compositions of the present invention.
Angelika Fretzen - Somerville MA, US Steven Witowski - Melrose MA, US Alfredo Grossi - Somerville MA, US Hong Zhao - Somerville MA, US Mahendra Dedhiya - Pomona NY, US Yun Mo - Commack NY, US
Assignee:
Ironwood Pharmaceuticals, Inc. - Cambridge MA Forest Laboratories Holdings Limited - Hamilton
International Classification:
A61K 38/12 A61P 1/00
US Classification:
514 211
Abstract:
The present invention relates to stable compositions comprising linaclotide, as well as to various methods and processes for the preparation and use of the compositions.
Stable Solid Formulation Of Therapeutic Polypeptides Suitable For Oral Administration
Angelika Fretzen - Somerville MA, US Steven Witowski - Melrose MA, US Alfredo Grossi - Somerville MA, US Hong Zhao - Somerville MA, US
Assignee:
Ironwood Pharmaceuticals, Inc. - Cambridge MA
International Classification:
A61K 9/14 A61K 9/00 A61K 9/48 A61K 38/02
US Classification:
424400, 514 11, 427 214
Abstract:
Solid, stable formulations of therapeutic polypeptide suitable for oral administration are described herein as are methods for preparing such formulations. The therapeutic polypeptide formulations described herein are stable and have a sufficient shelf life for manufacturing, storing and distributing the drug.
Stable Solid Formulations Of Gc-C Receptor Agonist Polypeptides Suitable For Oral Administration
Solid, stable formulations of GC-C receptor agonist polypeptide suitable for oral administration are described herein as are methods for preparing such formulations. The GC-C receptor agonist polypeptide formulations described herein are stable and have a sufficient shelf life for manufacturing, storing and distributing the drug.
Stable Solid Formulation Of A Gc-C Receptor Agonist Polypeptide Suitable For Oral Administration
Angelika Fretzen - Somerville MA, US Steven Witowski - Melrose MA, US Alfredo Grossi - Somerville MA, US Hong Zhao - Lexington MA, US Mahendra Dedhiya - Pomona NY, US Yun Mo - Commack NY, US
Assignee:
Forest Laboratories Holdings Limited - Hamilton Ironwood Pharmaceuticals, Inc. - Cambridge MA
Solid, stable formulations of linaclotide suitable for oral administration are described herein as are methods for preparing such formulations. The formulations described herein contain a polypeptide consisting of the amino acid sequence Cys Cys Glu Tyr Cys Cys Asn Pro Ala Cys Thr Gly Cys Tyr (“linaclotide”) or a pharmaceutically acceptable salt thereof. The linaclotide formulations described herein are stable and have a sufficient shelf life for manufacturing, storing and distributing the drug.
Pharmaceutical Composition And Administrations Thereof
William Rowe - Medford MA, US Patricia Hurter - Harvard MA, US Christopher R. Young - Waltham MA, US Kirk Dinehart - Holliston MA, US Marinus Jacobus Verwijs - Framingham MA, US Kirk Overhoff - Waltham MA, US Peter D.J. Grootenhuis - San Diego CA, US Martyn Botfield - Concord MA, US Alfredo Grossi - Somerville MA, US Gregor Zlokarnik - La Jolla CA, US Fredrick F. Van Goor - San Diego CA, US
Assignee:
Vertex Pharmaceuticals Incorporated - Cambridge MA
International Classification:
A61K 31/47 A61P 19/08 A61P 11/00 A61P 19/10
US Classification:
514312
Abstract:
The present invention relates to pharmaceutical compositions comprising a solid dispersion of N-[2,4-Bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide, methods of manufacturing pharmaceutical compositions of the present invention, and methods of administering pharmaceutical compositions of the present invention.