Tobira Therapeutics presents data on TBR-652 at the European AIDS Conference

December 21, 2015

TBR-652 was well-tolerated at single daily doses up to 800 mg and once-daily doses of up to 200 mg for 10 days. Headache, diarrhea, abdominal pain and nausea were the most commonly encountered treatment-emergent events; all AEs resolved by the end of both studies. "The results from these two Phase II studies provide further basis for the continued development of TBR-652 for the treatment of HIV," said James Sapirstein, CEO. "Providing patients with well-tolerated, once-daily dosing options is a priority with our development programs. We look forward to the results from our on-going proof of concept trial of TBR-652."

These data were presented at the 12th( )European AIDS Conference (EACS), held November 11-14, 2009 in Cologne, Germany. The poster presentation can be viewed at www.tobiratherapeutics.

SOURCE Tobira Therapeutics Inc.