Pfizer Suspends Chronic Pain Studies in Tanezumab Clinical Trial Program; Some Studies Continue in Areas of Unmet Medical Need
NEW YORK, July 19 /PRNewswire-FirstCall/ -- Pfizer Inc. (NYSE:PFE) today announced, at the request of the U.S. Food and Drug Administration (FDA), the suspension of the chronic low back pain and painful diabetic peripheral neuropathy studies in the clinical program for the investigational compound tanezumab. Investigation of the compound continues in some areas of high unmet medical need, including cancer pain.
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The FDA's request follows further consideration of reports of
adverse events in osteoarthritis patients taking tanezumab, and the
agency's concerns regarding the potential for such events in other
patient populations in which the compound is being studied. Pfizer
announced the suspension of tanezumab studies in patients with
osteoarthritis in a June 23 press release.
For studies on clinical hold, recruitment of new patients and the
dosing of existing patients are suspended.
Pfizer will continue to work with the FDA to reach a common
understanding about the appropriate scope of continued clinical
investigation of tanezumab.
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Our diversified global health care portfolio includes human and
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Consistent with our responsibility as the world's leading
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providers, governments and local communities to support and expand
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more than 150 years, Pfizer has worked to make a difference for all
who rely on us. To learn more about our commitments, please visit
us at www.pfizer.com.
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Source: Pfizer Inc.
CONTACT: Media Contact: MacKay Jimeson, +1-212-733-2324,
Mackay.Jimeson@Pfizer.com; or Investors Contact: Suzanne
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Web Site: http://www.pfizer.com/
Posted: July 2010
