J&J to discontinue aticaprant VENTURA program
US healthcare giant Johnson & Johnson (NYSE: JNJ) yesterday revealed that it has made the decision to discontinue the Phase III VENTURA development program evaluating aticaprant as an adjunctive treatment for major depressive disorder (aMDD) due to insufficient efficacy in the target patient population.
J&J noted that the data confirmed aticaprant is safe and well-tolerated, and no new safety signals were identified. Based on the potential for this mechanism, the company will explore future development opportunities for aticaprant in other areas of high unmet need. Full analyses from the VENTURA development program are underway and will be shared at a future medical meeting, J&J added.
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