Tenax Therapeutics’ heart-failure drug misses primary goal in Phase 3 trial, shares tumble
Tenax Therapeutics announced that its experimental oral levosimendan failed to meet the primary efficacy endpoint in the Phase 3 LEVEL study, which evaluated treatment for a form of heart failure linked to elevated pulmonary blood pressure.
The trial showed the drug improved six‑minute walk distance by 14 meters versus 10.4 meters for placebo, a difference that was not statistically significant, leading the company to deem the result negative.
Following the announcement, Tenax’s stock dropped sharply, falling about 84% to roughly $2 per share in early trading.
The outcome underscores the challenges of developing therapies for pulmonary‑hypertension‑related heart failure and may prompt the company to reassess its development strategy.
This writeup was produced by pharmadog from original reporting by STAT.
Original headline: “STAT+: Heart failure drug from Tenax Therapeutics fails in pivotal study”
read at STAT ↗
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