Literature DB >> 15035797

The CINOD, AZD3582, exhibits an improved gastrointestinal safety profile compared with naproxen in healthy volunteers.

Bror Jonzon1, Ingvar Bjarnason, Chris Hawkey, John Jones, Andrew Goddard, Urban Fagerholm, Pär Karlsson.   

Abstract

COX-inhibiting nitric oxide donators (CINODs) are a new class of drugs in development for the treatment of acute and chronic pain. They comprise a COX-inhibiting moiety linked to a nitric-oxide-donating component and are designed to provide an innovative mechanism of action of balanced COX inhibition and controlled nitric oxide donation. Through these pathways, CINODs should provide analgesic and anti-inflammatory efficacy, while offering gastrointestinal safety through the tissue-protective effects of nitric oxide donation. AZD3582 [4-(nitrooxy)butyl-(2S)-2-(6-methoxy-2-naphthyl)propanoate] is the first agent in the CINOD class to enter extensive clinical development. Pre-clinical studies demonstrate that AZD3582 has a superior gastrointestinal safety profile to naproxen, while demonstrating analgesic and anti-inflammatory efficacy. In healthy human volunteers, AZD3582 caused little gastrointestinal damage compared with equimolar doses of naproxen. Studies to evaluate the longer-term gastrointestinal safety of AZD3582, alongside its efficacy in alleviating chronic and acute pain, are ongoing.

Entities:  

Year:  2003        PMID: 15035797     DOI: 10.1163/156856003322699618

Source DB:  PubMed          Journal:  Inflammopharmacology        ISSN: 0925-4692            Impact factor:   4.473


  42 in total

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Journal:  J Rheumatol Suppl       Date:  1999-04

2.  Gastrointestinal safety of nitric oxide-derived aspirin is related to inhibition of ICE-like cysteine proteases in rats.

Authors:  S Fiorucci; E Antonelli; L Santucci; O Morelli; M Miglietti; B Federici; R Mannucci; P Del Soldato; A Morelli
Journal:  Gastroenterology       Date:  1999-05       Impact factor: 22.682

3.  Reduced incidence of gastroduodenal ulcers with celecoxib, a novel cyclooxygenase-2 inhibitor, compared to naproxen in patients with arthritis.

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Journal:  Am J Gastroenterol       Date:  2001-04       Impact factor: 10.864

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Journal:  Aliment Pharmacol Ther       Date:  1999-06       Impact factor: 8.171

5.  Uncoupling of intestinal mitochondrial oxidative phosphorylation and inhibition of cyclooxygenase are required for the development of NSAID-enteropathy in the rat.

Authors:  S Somasundaram; G Sigthorsson; R J Simpson; J Watts; M Jacob; I A Tavares; S Rafi; A Roseth; R Foster; A B Price; J M Wrigglesworth; I Bjarnason
Journal:  Aliment Pharmacol Ther       Date:  2000-05       Impact factor: 8.171

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Journal:  JAMA       Date:  2000-09-13       Impact factor: 56.272

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Journal:  Gastrointest Endosc Clin N Am       Date:  1996-07

8.  The effects of indomethacin on gastroduodenal morphology and mucosal pH gradient in the healthy human stomach.

Authors:  C J Shorrock; R J Prescott; W D Rees
Journal:  Gastroenterology       Date:  1990-08       Impact factor: 22.682

9.  A longterm endoscopic evaluation of patients with arthritis treated with nabumetone vs naproxen.

Authors:  S H Roth; R Bennett; P Caldron; C Mitchell; C Swenson; R Koepp
Journal:  J Rheumatol       Date:  1994-06       Impact factor: 4.666

10.  Double-blind comparison of efficacy and gastroduodenal safety of diclofenac/misoprostol, piroxicam, and naproxen in the treatment of osteoarthritis.

Authors:  J A Melo Gomes; S H Roth; J Zeeh; G A Bruyn; E M Woods; G S Geis
Journal:  Ann Rheum Dis       Date:  1993-12       Impact factor: 19.103

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  1 in total

1.  The impatient patient: a personal view of osteoarthritis.

Authors:  Michael C Powanda
Journal:  Inflammopharmacology       Date:  2003       Impact factor: 4.473

  1 in total

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