wo nucleoside
reverse transcriptase inhibitors (NRTIs), zidovudine + lamivudine (AZT/3TC)
or tenofovir + emtricitabine (TDF/FTC).
Safety Results
Of patients in the TMC278 combined group compared with EFV, 9 percent
vs. 21 percent experienced rash, 31 percent vs. 48 percent experienced
nervous system adverse events and 16 percent vs. 21 percent experienced
psychiatric events.
Overall, patients in the TMC278 combined group (all doses) vs. the EFV
group experienced similar incidences and types of serious adverse events
(SAEs) (12 percent vs. 15 percent), grade 3 or 4 adverse events (AEs), (27
percent vs. 21 percent) and grade 3 or 4 laboratory abnormalities (26
percent vs. 24 percent).
TMC278 is the third anti-HIV compound to be developed by Tibotec
Pharmaceuticals, which is also developing investigational compounds for the
treatment of hepatitis C and tuberculosis.
About Tibotec Pharmaceuticals Ltd.
Tibotec Pharmaceuticals Ltd., based in Cork, Ireland, is a
pharmaceutical research and development company. The Company's main
research and development facilities are in Mechelen, Belgium with offices
in Yardley, PA. Tibotec is dedicated to the discovery and development of
innovative HIV/AIDS drugs and anti-infectives for diseases of high unmet
medical need.
Media Contacts:
Karen Manson - 32-479-89-47-99
Pam Van Houten - 908-295-7367
Investor Relations Contacts:
Lesley Fishman - 732-542-3922
Louise Mehrota - 732-524-6491
'/>"/>SOURCE Tibotec Pharmaceuticals Ltd. Copyright©2008 PR Newswire. All rights reserved | |
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