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Tenax Therapeutics (TENX) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Tnx-103Pulmonary Hypertension Associated With HfpefPhase IIIEnrolling By InvitationLong-Term Open-Label Extension Study of Oral LevosimendanFeb 20, 2026―
Tnx-103Pulmonary Hypertension Associated With HfpefPhase IIIRecruitingLEVEL-2: LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF-2Dec 15, 2025
Tnx-103Pulmonary HypertensionPhase IIIRecruitingLEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEFAug 01, 2023
Levosimendan 2.5 Mg/Ml Injectable SolutionHeart Failure With Normal Ejection Fraction, Hypertension Pulmonary Secondary Heart Failure, Right Sided Heart Failure With Normal Ejection FractionPhase IICompletedOpen-Label Rollover Study of Levosimendan in PH-HFpEF PatientsJul 24, 2018―
LevosimendanHypertension Pulmonary Secondary, Heart Failure, Right Sided, Heart Failure With Normal Ejection FractionPhase IICompletedHemodynamic Evaluation of Levosimendan in Patients With PH-HFpEFMay 03, 2018―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Tenax Therapeutics (TENX) have in its pipeline
Tenax Therapeutics TENX is currently developing the following drugs: Tnx-103, Levosimendan 2.5 Mg/Ml Injectable Solution, Levosimendan. These drug candidates are in various stages of clinical development as the company works toward FDA approval.