Literature DB >> 25576073

CHF6001 II: a novel phosphodiesterase 4 inhibitor, suitable for topical pulmonary administration--in vivo preclinical pharmacology profile defines a potent anti-inflammatory compound with a wide therapeutic window.

Gino Villetti1, Chiara Carnini2, Loredana Battipaglia2, Laurent Preynat2, Pier Tonino Bolzoni2, Franco Bassani2, Paola Caruso2, Marco Bergamaschi2, Anna Rita Pisano2, Veronica Puviani2, Fabio Franco Stellari2, Valentina Cenacchi2, Roberta Volta2, Vittorio Bertacche2, Valentina Mileo2, Valentina Bagnacani2, Elisa Moretti2, Paola Puccini2, Silvia Catinella2, Fabrizio Facchinetti2, Angelo Sala2, Maurizio Civelli2.   

Abstract

CHF6001 [(S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyloxy)ethyl)pyridine 1-oxide] is a novel phosphodiesterase 4 (PDE4) inhibitor designed for use in pulmonary diseases by inhaled administration. Intratracheal administration of CHF6001 to ovalbumin-sensitized Brown-Norway rats suppressed the antigen-induced decline of lung functions (ED50 = 0.1 µmol/kg) and antigen-induced eosinophilia (ED50 = 0.03 µmol/kg) when administered (0.09 μmol/kg) up to 24 hours before antigen challenge, in agreement with CHF6001-sustained lung concentrations up to 72 hours after intratracheal treatment (mean residence time 26 hours). Intranasal, once daily administration of CHF6001 inhibited neutrophil infiltration observed after 11 days of tobacco smoke exposure in mice, both upon prophylactic (0.15-0.45 µmol/kg per day) or interventional (0.045-0.45 µmol/kg per day) treatment. CHF6001 was ineffective in reversing ketamine/xylazine-induced anesthesia (a surrogate of emesis in rat) up to 5 µmol/kg administered intratracheally, a dose 50- to 150-fold higher than anti-inflammatory ED50 observed in rats. When given topically to ferrets, no emesis and nausea were evident up to 10 to 20 µmol/kg, respectively, whereas the PDE4 inhibitor GSK-256066 (6-[3-(dimethylcarbamoyl)phenyl]sulfonyl-4-(3-methoxyanilino)-8-methylquinoline-3-carboxamide) induced nausea at 1 µmol/kg intratracheally. A 14-day inhalation toxicology study in rats showed a no-observed-adverse-effect level dose of 4.4 µmol/kg per day for CHF6001, lower than the 0.015 μmol/kg per day for GSK-256066. CHF6001 was found effective and extremely well tolerated upon topical administration in relevant animal models, and may represent a step forward in PDE4 inhibition for the treatment of asthma and chronic obstructive respiratory disease.
Copyright © 2015 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2015        PMID: 25576073     DOI: 10.1124/jpet.114.220558

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  17 in total

1.  The COPD Pipeline XXXVIII.

Authors:  Nicholas Gross
Journal:  Chronic Obstr Pulm Dis       Date:  2018-01-18

Review 2.  Inhaled Phosphodiesterase Inhibitors for the Treatment of Chronic Obstructive Pulmonary Disease.

Authors:  Dave Singh; Simon Lea; Alexander G Mathioudakis
Journal:  Drugs       Date:  2021-11-03       Impact factor: 9.546

Review 3.  Emerging pharmaceutical therapies for COPD.

Authors:  Sowmya P Lakshmi; Aravind T Reddy; Raju C Reddy
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2017-07-21

4.  Phosphodiesterase 4 inhibitors attenuate virus-induced activation of eosinophils from asthmatics without affecting virus binding.

Authors:  Yanaika Shari Sabogal Piñeros; Tamara Dekker; Barbara Smids; Christof J Majoor; Lara Ravanetti; Gino Villetti; Maurizio Civelli; Fabrizio Facchinetti; René Lutter
Journal:  Pharmacol Res Perspect       Date:  2020-06

5.  Safety, tolerability, and pharmacokinetics of single and repeat ascending doses of CHF6001, a novel inhaled phosphodiesterase-4 inhibitor: two randomized trials in healthy volunteers.

Authors:  Fabrizia Mariotti; Mirco Govoni; Germano Lucci; Debora Santoro; Marie Anna Nandeuil
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2018-10-18

6.  Effect of the inhaled PDE4 inhibitor CHF6001 on biomarkers of inflammation in COPD.

Authors:  Dave Singh; Kai Michael Beeh; Brendan Colgan; Oliver Kornmann; Brian Leaker; Henrik Watz; Germano Lucci; Silvia Geraci; Aida Emirova; Mirco Govoni; Marie Anna Nandeuil
Journal:  Respir Res       Date:  2019-08-09

7.  Concentration-QT Modeling Following Inhalation of the Novel Inhaled Phosphodiesterase-4 Inhibitor CHF6001 in Healthy Volunteers Shows an Absence of QT Prolongation.

Authors:  Koen Jolling; Angela Äbelö; Nicolas Luyckx; Marie-Anna Nandeuil; Mirco Govoni; Massimo Cella; Andreas Lindauer
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2019-05-11

8.  Anti-inflammatory effects of the novel inhaled phosphodiesterase type 4 inhibitor CHF6001 on virus-inducible cytokines.

Authors:  Michael R Edwards; Fabrizio Facchinetti; Maurizio Civelli; Gino Villetti; Sebastian L Johnston
Journal:  Pharmacol Res Perspect       Date:  2016-01-15

9.  Synthesis, Pharmacological Profile and Docking Studies of New Sulfonamides Designed as Phosphodiesterase-4 Inhibitors.

Authors:  Isabelle Karine da Costa Nunes; Everton Tenório de Souza; Suzana Vanessa S Cardozo; Vinicius de Frias Carvalho; Nelilma Correia Romeiro; Patrícia Machado Rodrigues E Silva; Marco Aurélio Martins; Eliezer J Barreiro; Lídia Moreira Lima
Journal:  PLoS One       Date:  2016-10-03       Impact factor: 3.240

Review 10.  Phosphodiesterase-4 Inhibitors for the Treatment of Inflammatory Diseases.

Authors:  Heng Li; Jianping Zuo; Wei Tang
Journal:  Front Pharmacol       Date:  2018-10-17       Impact factor: 5.810

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