Abstract: Compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders, or conditions associated with one or more of the lysophosphatidic acid receptors are provided.
Type:
Application
Filed:
August 14, 2012
Publication date:
March 21, 2013
Applicant:
InterMune, Inc.
Inventors:
Brad O. Buckman, John B. Nicholas, Kumaraswamy Emayan, Scott D. Seiwert
Abstract: A capsule formulation of pirfenidone is provided that includes pharmaceutically acceptable excipients. In one embodiment, this capsule formulation is capable of sustaining desirable pharmacokinetic responses in a patient. Further provided are methods of treating fibrotic conditions and other cytokine-mediated disorders by administering pirfenidone capsules of such formulation to a patient in need.
Type:
Grant
Filed:
June 16, 2011
Date of Patent:
February 26, 2013
Assignee:
Intermune, Inc.
Inventors:
Ramachandran Radhakrishnan, Ronald Vladyka, Kenneth Sultzbaugh
Abstract: The present invention relates to methods involving avoiding adverse drug interactions with fluvoxamine and pirfenidone or other moderate to strong inhibitors of CYP enzymes.
Type:
Application
Filed:
December 3, 2010
Publication date:
January 31, 2013
Applicant:
INTERMUNE ,INC.
Inventors:
Williamson Z. Bradford, Javier Szwarcberg
Abstract: The present invention relates to methods involving avoiding adverse drug interactions with fluvoxamine and pirfenidone or other moderate to strong inhibitors of CYP enzymes.
Type:
Grant
Filed:
September 2, 2011
Date of Patent:
November 27, 2012
Assignee:
Intermune, Inc.
Inventors:
Williamson Ziegler Bradford, Javier Szwarcberg
Abstract: Disclosed are compounds and methods for treating inflammatory and fibrotic disorders, including methods of modulating a stress activated protein kinase (SAPK) system with an active compound, wherein the active compound exhibits low potency for inhibition of the p38 MAPK; and wherein the contacting is conducted at a SAPK-modulating concentration that is at a low percentage inhibitory concentration for inhibition of the p38 MAPK by the compound. Also disclosed are derivatives and analogs of pirfenidone, useful for modulating a stress activated protein kinase (SAPK) system.
Type:
Grant
Filed:
June 3, 2009
Date of Patent:
November 6, 2012
Assignee:
Intermune, Inc.
Inventors:
Karl Kossen, Scott D. Seiwert, Vladimir Serebryany, Donald Ruhrmund, Leonid Beigelman, Luca Francesco Mario Raveglia, Stefania Vallese, Ivana Bianchi, Tao Hu
Abstract: The embodiments provide compounds of the general Formulae I through general Formula VIII, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
Type:
Grant
Filed:
April 19, 2012
Date of Patent:
October 30, 2012
Assignee:
InterMune, Inc.
Inventors:
Lawrence M Blatt, Scott D Seiwert, Steven W Andrews, Pierre Martin, Andreas Schumacher, Bradley Barnett, C. Todd Eary, Robert Kaus, Timothy Kercher, Weidong Liu, Michael Lyon, Paul Nichols, Bin Wang, Tarek Sammakia, April Kennedy, Yutong Jiang
Abstract: Disclosed are methods of modulating a stress activated protein kinase (SAPK) system with an active compound, wherein the active compound exhibits low potency for inhibition of at least one p38 MAPK; and wherein the contacting is conducted at a SAPK-modulating concentration that is at a low percentage inhibitory concentration for inhibition of the at least one p38 MAPK by the compound. Also disclosed are derivatives of pirfenidone. These derivatives can modulate a stress activated protein kinase (SAPK) system.
Type:
Application
Filed:
June 20, 2012
Publication date:
October 11, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Lawrence M. Blatt, Scott D. Seiwert, Leonid Beigelman, Ramachandran Radhakrishnan, Karl Kossen, Vladimir Serebryany
Abstract: The embodiments provide compounds of the general Formulae I through general Formula VIII, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
Type:
Application
Filed:
April 19, 2012
Publication date:
August 16, 2012
Applicants:
Array BioPharma, Inc., InterMune, Inc.
Inventors:
Lawrence M. Blatt, Scott D. Seiwert, Steven W. Andrews, Pierre Martin, Andreas Schumacher, Bradley Barnett, C. Todd Eary, Robert Kaus, Timothy Kercher, Weidong Liu, Michael Lyon, Paul Nichols, Bin Wang, Tarek Sammakia, April Kennedy, Yutong Jiang
Abstract: The embodiments provide compounds of the general Formulae I, Ia, II, IIa, III, IIIa, IV, IVa, V, Va, VI and VIa, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
Type:
Application
Filed:
October 21, 2011
Publication date:
April 26, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Brad BUCKMAN, Vladimir SEREBRYANY, John B. NICHOLAS, Scott SEIWERT
Abstract: The embodiments provide compounds of the general Formulae I, Ia, II, IIa, III, IIIa, IIIb, IV, IVa, IVb, V, Va, Vb, VI, VIa, VIb, and VIc, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition. The embodiments also provide methods for the synthesis of subject compounds and intermediates in the synthetic methods.
Type:
Application
Filed:
September 20, 2011
Publication date:
April 19, 2012
Applicant:
InterMune, Inc.
Inventors:
Brad Buckman, John B. Nicholas, Vladimir Serebryany, Scott D. Seiwert
Abstract: The embodiments provide compounds of the general Formulae I, and II, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
Type:
Application
Filed:
September 14, 2011
Publication date:
April 19, 2012
Applicant:
InterMune, Inc.
Inventors:
Brad Buckman, John B. Nicholas, Vladimir Serebryany, Scott D. Seiwert
Abstract: Methods are provided for administering pirfenidone to a patient that has exhibited abnormal biomarkers of liver function in response to pirfenidone administration. The methods include administering to a patient pirfenidone at doses lower than the full target dosage for a time period, followed by administering to the patient pirfenidone at the full target dosage. The methods also include administering pirfenidone at the full target dose with no reduction and administering permanently reduced doses of pirfenidone.
Type:
Application
Filed:
December 6, 2011
Publication date:
March 29, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Williamson Z. Bradford, Javier Szwarcberg
Abstract: Macrocyclic compounds having the structures described herein are useful for inhibiting replication of the hepatitis C virus (HCV). In preferred embodiments, the compounds are active against both the NS3 protease and the NS3 helicase of HCV.
Type:
Grant
Filed:
October 10, 2006
Date of Patent:
February 21, 2012
Assignee:
InterMune, Inc.
Inventors:
Leonid Beigelman, Scott D. Seiwert, Lawrence Blatt, Steven Andrews, Julia Haas
Abstract: The present invention relates to methods involving avoiding adverse drug interactions with fluvoxamine and pirfenidone or other moderate to strong inhibitors of CYP enzymes.
Type:
Application
Filed:
September 26, 2011
Publication date:
January 19, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Williamson Z. Bradford, Javier Szwarcberg
Abstract: A process for synthesizing pirfenidone from bromobenzene having less than about 0.15% by weight dibromobenze is disclosed. Also disclosed are processes of synthesizing pirfenidone without using ethyl acetate or n-butanol, and pirfenidone having controlled levels of ethyl acetate, n-butanol, di(5-methyl-2-pyridinone)benzenes, and other impurities having specified retention times. Also disclosed are formulated dosage forms including the disclosed pirfenidone.
Type:
Application
Filed:
September 26, 2011
Publication date:
January 19, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Sabine M. Pyles, Michael Cyr, Ramachandran Radhakrishnan
Abstract: A capsule formulation of pirfenidone is provided that includes pharmaceutically acceptable excipients. In one embodiment, this capsule formulation is capable of sustaining desirable pharmacokinetic responses in a patient. Further provided are methods of treating fibrotic conditions and other cytokine-mediated disorders by administering pirfenidone capsules of such formulation to a patient in need.
Type:
Application
Filed:
June 16, 2011
Publication date:
January 19, 2012
Applicant:
INTERMUNE, INC.
Inventors:
Ramachandran Radhakrishnan, Ronald Vladyka, Kenneth Sultzbaugh
Abstract: The invention relates to methods of treating patients infected with human immunodeficiency virus (HIV) with a therapeutic that has anti-fibrotic effects, for example, pirfenidone and analogs thereof.
Type:
Application
Filed:
September 26, 2011
Publication date:
January 19, 2012
Applicants:
University of Minnesota, INTERMUNE, INC.
Inventors:
Karl Kossen, Timothy Schacker, Ashley T. Haase