Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

ONO-6818 Cortech/Ono.

Alexandre Trifilieff1

  • 1Novartis Respiratory Research Centre, Horsham, West Sussex, UK. alexandre.trifilieff@pharma.novartis.com

Current Opinion in Investigational Drugs (London, England : 2000)
|September 5, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Discovery and Optimization of 4-(8-(3-Fluorophenyl)-1,7-naphthyridin-6-yl)transcyclohexanecarboxylic Acid, an Improved PDE4 Inhibitor for the Treatment of Chronic Obstructive Pulmonary Disease (COPD).

Journal of medicinal chemistry·2015
Same author

Comparing the cardiovascular therapeutic indices of glycopyrronium and tiotropium in an integrated rat pharmacokinetic, pharmacodynamic and safety model.

Toxicology and applied pharmacology·2015
Same author

The identification of 7-[(R)-2-((1S,2S)-2-benzyloxycyclopentylamino)-1-hydroxyethyl]-4-hydroxybenzothiazolone as an inhaled long-acting β2-adrenoceptor agonist.

Bioorganic & medicinal chemistry letters·2014
Same author

An investigation into the structure-activity relationships associated with the systematic modification of the β(2)-adrenoceptor agonist indacaterol.

Bioorganic & medicinal chemistry letters·2012
Same author

Solubility-driven optimization of phosphodiesterase-4 inhibitors leading to a clinical candidate.

Journal of medicinal chemistry·2012
Same author

The Influence of receptor kinetics on the onset and duration of action and the therapeutic index of NVA237 and tiotropium.

The Journal of pharmacology and experimental therapeutics·2012

ONO-6818, an orally bioavailable neutrophil elastase inhibitor, is being investigated for inflammatory conditions like rheumatoid arthritis and COPD. Early-stage clinical trials were ongoing in Japan and the US, with unconfirmed reports suggesting progression to Phase II studies.

Area of Science:

  • Pharmacology
  • Drug Development
  • Inflammation Research

Background:

  • ONO-6818 is a neutrophil elastase inhibitor developed for inflammatory diseases.
  • It is orally bioavailable and licensed from Cortech by Ono Pharmaceuticals.
  • Potential therapeutic applications include rheumatoid arthritis, inflammatory bowel disease, and COPD.

Purpose of the Study:

  • To evaluate the safety and efficacy of ONO-6818 in early-phase clinical trials.
  • To assess the compound's potential for treating inflammatory conditions.

Main Methods:

  • Phase I clinical trials conducted in Japan and the US.
  • Ongoing investigations into ONO-6818's pharmacokinetic and pharmacodynamic properties.

Main Results:

Related Experiment Videos

  • Phase I trials for COPD were initiated in Japan by December 1999.
  • Phase I trials were ongoing in Japan and the US as of September 2001.
  • Unconfirmed reports in June 2002 indicated progression to Phase II trials in Japan and preparation for Phase II in the US.

Conclusions:

  • ONO-6818 demonstrated progression through early-stage clinical development for COPD.
  • Further investigation in Phase II trials was anticipated for the US and Japan.