12:00 AM
Mar 30, 1998
 |  BC Week In Review  |  Clinical News  |  Clinical Results

Lamivudine 3TC: Phase III; awaiting marketing approval

BCHE reported data from trials comparing the combination of lamivudine with Intron A versus either alone. A total of 226 patients were randomized to received 100 mg lamivudine once daily for 52 weeks, 10 MU Intron A three times weekly for 16 weeks or lamivudine for 8 weeks followed by combination treatment for 16 weeks. Patients were followed to week 64.

The primary end point was seroconversion...

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