DURECT Starts Phase II Dosing for TRANSDUR(TM)-Bupivacaine (DUR-843)
CUPERTINO, Calif., Jan 03, 2007 /PRNewswire-FirstCall via COMTEX News Network/ — DURECT Corporation (Nasdaq: DRRX) today announced that we have started Phase II dosing in the U.S. under an FDA-accepted Investigational New Drug (IND) application for TRANSDUR(TM)-Bupivacaine (DUR-843), a transdermal pain patch for patients suffering from Post-Herpetic Neuralgia (post-shingles pain or PHN). DURECT’s Phase I […]
DURECT Starts Phase II Dosing for TRANSDUR(TM)-Bupivacaine (DUR-843) Read More »
