Tenax Therapeutics Says Late-Stage Trial Misses Primary, Secondary Endpoints
By Connor Hart
Tenax Therapeutics said a late-stage clinical trial of its treatment for pulmonary hypertension failed to meet its primary or key secondary endpoints.
The company on Monday said the treatment, TNX-103, didn't result in a statistically significant improvement in six-minute walk distances versus placebo, or improvement in Kansas City Cardiomyopathy Questionnaire total symptom score.
Shares of Tenax tumbled 85%, to $2.07, in premarket trading.
Still, Tenax said it has identified a substantial beneficial treatment effect in patients with greater disease burden, and that the treatment was generally safe and well tolerated.
The company said it intends to request a Type C Meeting with the Food and Drug Administration to discuss revisions to the ongoing registrational development of TNX-103 for the treatment of pulmonary hypertension due to heart failure with preserved ejection fraction.
"Having reviewed the available trial results, I am encouraged we have a clear path forward," Stuart Rich.
Write to Connor Hart at connor.hart@wsj.com
(END) Dow Jones Newswires
August 10, 2026 07:52 ET (11:52 GMT)
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