Abstract: 1-Phenyl-2-pyridinyl alkyl alcohol compounds are effective as inhibitors of the phosphodiesterase 4 (PDE4) enzyme and may be used to prevent and/or treat certain diseases or conditions.
Abstract: Compounds of formula (I) described herein are both phosphodiesterase 4 (PDE4) enzyme inhibitors and muscarinic M3 receptor antagonists and are useful for the prevention and/or treatment of diseases of the respiratory tract characterized by airway obstruction.
Type:
Application
Filed:
December 4, 2014
Publication date:
June 11, 2015
Applicant:
CHIESI FARMACEUTICI S.P.A.
Inventors:
Gabriele AMARI, Elisabetta ARMANI, Eleonora GHIDINI, Charles BAKER-GLENN, Hervé VAN DE POËL, Ben WHITTAKER
Abstract: Compounds having a benzhydryl structure represented by formula (I) described herein are both phosphodiesterase 4 (PDE4) enzyme inhibitors and muscarinic M3 receptor antagonists and are useful for treating diseases of the respiratory tract.
Type:
Application
Filed:
December 4, 2014
Publication date:
June 11, 2015
Applicant:
CHIESI FARMACEUTICI S.p.A.
Inventors:
Gabriele AMARI, Elisabetta Armani, Carmelida Capaldi, Renato De Fanti, Mauro Riccaboni, Charles Baker-Glenn, Hervé Van De Poël
Abstract: Compounds of formula (I) defined herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.
Type:
Application
Filed:
January 30, 2015
Publication date:
May 21, 2015
Applicant:
CHIESI FARMACEUTICI S.p.A.
Inventors:
Fabio RANCATI, Ian Linney, Chris Knight, Wolfgang Schmidt
Abstract: Compounds of formula (I) described herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.
Abstract: Compounds of formula (I): wherein R2, W, A, Y, and R1 are as defined in the specification, and pharmaceutically acceptable salts thereof, are p38 MAPK inhibitors, and are useful as anti-inflammatory agents in the treatment of, inter alia, diseases of the respiratory tract.
Type:
Grant
Filed:
August 5, 2014
Date of Patent:
May 12, 2015
Assignee:
Chiesi Farmaceutici S.p.A.
Inventors:
Monique Bodil Van Niel, Nicholas Charles Ray, Andrew Peter Cridland, Christopher Hurley, Lilian Alcaraz, Terry Aaron Panchal, Andrew Stephen Robert Jennings, Elisabetta Armani
Abstract: Compounds, pyridine N-oxides, and pharmaceutically acceptable salts of formula (I) are useful as inhibitors of the phosphodiesterase 4 (PDE4) enzyme and for preventing and/or treating diseases of the respiratory tract characterized by airway obstruction, such as asthma or COPD.
Type:
Grant
Filed:
October 19, 2012
Date of Patent:
May 5, 2015
Assignee:
Chiesi Farmaceutici S.p.A.
Inventors:
Elisabetta Armani, Gabriele Amari, Carmelida Capaldi, Laura Carzaniga, Elena La Porta, Matilde Guala
Abstract: The present invention relates to a process for the preparation of compounds endowed with phosphodiesterase (PDE4) inhibitory activity having formula (I). The invention also relates to the process for the isolation by crystallization of the compound (I) and to its use for the preparation of pharmaceutical compositions for inhalation in combination with suitable carriers or vehicles. The present invention also relates to solvates and crystal forms of a compound of formula (I). The synthesized product is suitable for use in pharmaceutical applications for instance in the treatment of respiratory diseases.
Abstract: Compounds of formula (I) act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for treating and/or preventing broncho-obstructive and inflammatory diseases.
Type:
Grant
Filed:
June 8, 2012
Date of Patent:
April 21, 2015
Assignee:
Chiesi Farmaceutici S.p.A.
Inventors:
Fabio Rancati, Andrea Rizzi, Ian Linney, Wesley Blackaby, Chris Knight
Abstract: Cohesive high-dosage strength micronized active ingredients may be dispersed in dry powder formulations for inhalation comprising carrier particles, by use of the apparatus described herein.
Abstract: Compounds of formula (I) described herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.
Abstract: Compounds of formula (I) and pharmaceutically acceptable salts thereof: wherein R2, W, A, Y and R1 are as defined in the specification, are p38 MAPK inhibitors, and are useful as anti-inflammatory agents in the treatment of, inter alia, diseases of the respiratory tract.
Type:
Application
Filed:
October 14, 2014
Publication date:
March 19, 2015
Applicant:
CHIESI FARMACEUTICI S.p.A.
Inventors:
Monique Bodil Van Niel, Nicholas Charles Ray, Lilian Alcaraz, Terry Aaron Panchal, Andrew Stephen Robert Jennings, Elisabetta Armani, Andrew Peter Cridland, Christopher Hurley
Abstract: Compounds of formula (I) defined herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.
Type:
Grant
Filed:
December 6, 2013
Date of Patent:
March 17, 2015
Assignee:
Chiesi Farmaceutici S.p.A.
Inventors:
Fabio Rancati, Ian Linney, Chris Knight, Wolfgang Schmidt
Abstract: Carrier particles in which at least 60% of the surface is coated with magnesium stearate are useful for preparing dry powder formulations for inhalation.
Abstract: Administration of certain 1-phenylalkanecarboxylic acid derivatives is useful for treating, preventing and/or reducing the risk of developing Alzheimer's Disease and multiple sclerosis.
Type:
Application
Filed:
August 15, 2014
Publication date:
March 5, 2015
Applicant:
Chiesi Farmaceutici S.p.A.
Inventors:
Bruno Imbimbo, Marina Pizzi, Daniel Chain
Abstract: Anti-inflammatory and antiallergic compounds of the glucocorticosteroid series, according to formula (I) according to formula (I) defined herein are useful for treating diseases of the respiratory tract characterized by airway obstruction.
Abstract: Disclosed are compounds having [1,2,4]triazolo[4,3-a]pyridine groups and pharmaceutically acceptable salts thereof. The compounds are p38 MAPK inhibitors, useful as anti-inflammatory agents in the treatment of, inter alia, diseases of the respiratory tract.
Type:
Application
Filed:
December 9, 2011
Publication date:
February 26, 2015
Applicant:
Chiesi Farmaceutici S.p.A.
Inventors:
Harry Finch, Monique Bodil Van Niel, Chi-Kit Woo
Abstract: The subject invention provides compounds of formula (I): Including monomers and multimers thereof that are inhibitors of human neutrophil elastase (HNE) activity and are useful in the treatment of diseases or conditions in which HNE plays a part.
Type:
Grant
Filed:
April 17, 2012
Date of Patent:
February 17, 2015
Assignee:
Chiesi Farmaceutici S.p.A
Inventors:
Nicholas Charles Ray, Harry Finch, Christine Edwards, Elizabeth O'Connor