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Teva Announces New Olanzapine LAI (TEV-'749) Post Hoc Data Highlighting High Rates of ...

Published

18 September 2026

Topic

opportunities

◆ Sectors

Biotech

◆ Geography

United States

◆ Source

Read at ir.tevapharm.com →

◆ Verified

Fusion42 · 18 September 2026 · Fusion42 review

Teva presented new post hoc data from the Phase 3 SOLARIS trial showing that its once-monthly subcutaneous injectable olanzapine (TEV-'749) achieved high rates of stabilization and remission with low relapse rates in adults with schizophrenia. The data also support safe switching from oral or short-acting injectable olanzapine to TEV-'749, ahead of an FDA approval decision expected in Q4 2026.

This Wire brief sits within Fusion42's coverage of Biotech, and 2 sources have reported it between 18 Sep 2026 and 19 Sep 2026.

◆ ◆ The Wire takeaway

You can now position to serve patients shifting from daily oral olanzapine to a monthly injectable as the FDA nears approval. Switching treatments without losing efficacy opens a valuable patient segment that daily pills struggle to retain.

◆ Coverage

2 sources · first reported 18 Sep 2026 · latest 19 Sep 2026

◆ Related on Wire

◆ Topics

Biotechschizophrenialong-acting-injectableolanzapineclinical-trialFDA-approvalneuroscience