Biotech & Genomic Medicine▼
J&J and Contineum's Depression Drug Misses Phase 2 Primary Endpoint
Contineum Therapeutics said JNJ-5120/PIPE-307, a drug Johnson & Johnson is advancing under a global license and development agreement, failed to hit the primary endpoint of the Phase 2 MOONLIGHT-1 study in major depressive disorder. The trial enrolled 107 adults with MDD and tested the drug as a monotherapy, measuring change from baseline in the Montgomery-Åsberg Depression Rating Scale total score at Day 5 versus placebo. Contineum said the drug was well tolerated with no new safety signals, and Johnson & Johnson has not announced that development is ending, saying it is still analyzing the broader dataset including prespecified exploratory endpoints before deciding next steps. It is the second disappointing efficacy readout for PIPE-307, after a 2025 study of the same compound in relapsing-remitting multiple sclerosis failed its primary efficacy measure. Contineum continues to advance its internally developed PIPE-791 program in indications including idiopathic pulmonary fibrosis and chronic pain, leaving J&J's decision on PIPE-307 as the next concrete milestone.
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CTNM · Technology · Negative Contineum's licensed PIPE-307/JNJ-5120 failed the Phase 2 MOONLIGHT-1 primary endpoint in major depressive disorder, its second efficacy miss.
JNJ · Technology · Negative J&J's licensed depression drug JNJ-5120/PIPE-307 missed the Phase 2 primary endpoint, though J&J is still analyzing data before deciding next steps.