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Aventis not to seek regulatory approval for cariporide
Strasbourg, France | Monday, May 19, 2003, 08:00 Hrs  [IST]

In July 2002, Aventis had announced the termination of patient enrollment in the Expedition trial involving the cardiovascular drug candidate cariporide, following a recommendation by an independent Drug Safety Monitoring Board. This trial was a phase III drug-intervention study in coronary artery bypass (CABG) patients.

Upon completion of the analysis of the overall benefit-risk assessment, Aventis has concluded that the results do not support a regulatory submission for cariporide.

Aventis is dedicated to treating and preventing disease by discovering and developing innovative prescription drugs and human vaccines. In 2002, Aventis generated sales of € 17.6 billion, invested € 3.1 billion in research and development.

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