Tenax's TNX-103 misses primary endpoint in Phase 3 LEVEL trial for PH-HFpEF
Subgroup analyses showed benefit in sicker patients, and the company plans to seek an FDA meeting to discuss adjusting the registrational program.
SEC filing
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Subgroup analyses showed benefit in sicker patients, and the company plans to seek an FDA meeting to discuss adjusting the registrational program.
SEC filing
Tenax says topline Phase 3 LEVEL results are expected in August 2026 and will be presented at the ESC Congress, while enrollment continues in a second pivotal trial, LEVEL-2.
SEC filing