Tanox Reports Positive Results From Phase 2 Clinical Trial of TNX-355, an Entry Inhibitor to Treat HIV
26 Outubro 2005 - 7:00AM
PR Newswire (US)
Trial Meets Primary Endpoint HOUSTON, Oct. 26
/PRNewswire-FirstCall/ -- Tanox, Inc. (NASDAQ:TNOX) today reported
positive Phase 2 clinical results of its novel HIV drug candidate,
TNX-355. The 24-week results of the study show that TNX-355 at the
10 mg/kg dose, when given in combination with optimized background
therapy (OBT), produced a considerably greater reduction in viral
load in HIV-infected patients than did placebo in combination with
OBT. TNX-355 was well tolerated, with no serious adverse events
related to the drug. The study met its primary endpoint with
TNX-355 plus OBT demonstrating a statistically significant
reduction in viral load -- the level of HIV in the bloodstream --
compared to placebo plus OBT at Week 24. Treatment with the 10
mg/kg dose of TNX-355 resulted in a viral-load reduction of 1.16
log10, compared with a 0.20 log10 reduction in the placebo group,
representing a 0.96 log10 greater reduction (p
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