Triangle Pharmaceuticals has announced that development of the non-nucleoside reverse transcriptase inhibitor emivirine (Coactinon) is to be halted following an interim analysis of a trial comparing emivirine with abacavir (study MKC-401), in which all participants also received d4T and FTC. Viral load suppression was significantly poorer in the emivirine arm compared to the abacavir arm.
Emivirine is one of five agents under development by Triangle, but its progress has been slow and results from earlier phase III studies had not been particularly strong. In an unusual move, the FDA asked Triangle to design a new study in late 1999 that would combine test emivirine with another of the company’s unlicensed agents, FTC.
Triangle also announced yesterday that it is moving forward with plans to submit a new drug application to the Food and Drug Administration for FTC (emtricitabine) in the fourth quarter of 2002. FTC (Coviracil) is a once daily nucleoside analogue with a similar resistance pattern to 3TC, and is also active against hepatitis B. Abbott Laboratories will handle marketing of Coviracil worldwide.
Triangle’s decision to drop emivirine is largely driven by a cash shortage; it has taken the company longer than expected to bring one of its agents to market. Last October the company shed a third of its staff and
The company also admitted that it had no further plans to develop mozenavir, a once daily protease inhibitor, despite showing comparability with indinavir in a Phase III study reported at last summer’s International AIDS Society conference in Buenos Aires. Mozenavir’s future is uncertain; despite promising results, the drug cannot be boosted with ritonavir, does not appear to carry a reduced risk of metabolic disturbances and is not active against virus already resistant to ritonavir or indinavir.