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An efficient randomised, placebo-controlled clinical trial with the irreversible fatty acid amide hydrolase-1 inhibitor PF-04457845, which modulates endocannabinoids but fails to induce effective analgesia in patients with pain due to osteoarthritis of the knee

Huggins, John P.*; Smart, Trevor S.; Langman, Stephen; Taylor, Louise; Young, Tim

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doi: 10.1016/j.pain.2012.04.020
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Summary A randomised, placebo-controlled clinical trial with PF-04457845, a novel irreversible fatty acid amide hydrolase-1 inhibitor, increases endocannabinoids, but does not induce analgesia in patients with osteoarthritis.

The effect of PF-04457845, a potent and selective fatty acid amide hydrolase-1 (FAAH1) inhibitor, on pain due to osteoarthritis of the knee was investigated in a randomised placebo and active-controlled clinical trial. The trial involved 2 periods (separated by a 2-week washout) consisting of a 1-week wash-in phase followed by 2 weeks double-blind treatment. Patients received single-blind placebo throughout the wash-in and washout periods. Patients were randomised to receive either 4 mg q.d. PF-04457845 followed by placebo (or vice versa), or 500 mg b.i.d. naproxen followed by placebo (or vice versa). The primary end point was the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain score. The trial had predefined decision rules based on likelihood that PF-04457845 was better or worse than the standard of care (considered to be a 1.8 reduction in WOMAC pain score compared to placebo). A total of 74 patients were randomised to 1 of 4 treatment sequences. The mean differences (80% confidence intervals) from placebo in WOMAC pain score were 0.04 (−0.63 to 0.71) for PF-04457845 and −1.13 (−1.79 to −0.47) for naproxen, indicating that whilst naproxen seemed efficacious, PF-04457845 was not differentiated from placebo. The study was stopped at the interim analysis for futility. PF-04457845 decreased FAAH activity by >96% and substantially increased 4 endogenous substrates (fatty acid amides). PF-04457845 was well tolerated in osteoarthritis patients, and there was no evidence of cannabinoid-type adverse events. The lack of analgesic effect of FAAH1 inhibition in humans is in contrast to data from animal models. This apparent disconnect between species needs further study.

Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

Pfizer Global Research and Development, Sandwich, UK

*Corresponding author. Address: JPH Pharma, Dayspring, 21 Rectory Road, Deal, Kent CT14 9LY, UK. Tel.: +44 (0)1304 379010.

E-mail address:johnphuggins@btinternet.com

© 2012 Lippincott Williams & Wilkins, Inc.
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