Neoprobe gets FDA nod for more Lymphoseek trials

AuntMinnie.com staff writers
Jan 16, 2007

Gamma camera probe developer Neoprobe has received authorization from the U.S. Food and Drug Administration (FDA) to begin patient enrollment in two phase I clinical studies for its Lymphoseek targeting agent.

The two studies, to be undertaken at the University of California, San Diego, will evaluate the safety and efficacy of Lymphoseek in prostate and colon cancers. The National Cancer Institute has provided grants for the studies, according to Neoprobe of Dublin, OH.

By AuntMinnie.com staff writers
January 17, 2007

Related Reading

Neoprobe debuts Bluetooth probe, October 10, 2006

Neoprobe, Estech ink distribution deal, September 11, 2006

Neoprobe to start Lymphoseek trial, July 13, 2006

Neoprobe, Estech ink deal, June 8, 2006

Neoprobe revenues climb in Q1, May 2, 2006

Copyright © 2007 AuntMinnie.com

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