TENXNasdaqPharmaceutical PreparationsUS GAAP · USD

Tenax Therapeutics, Inc

Tenax Therapeutics, Inc. is a U.S.-based clinical-stage pharmaceutical company focused on developing cardiopulmonary therapies for pulmonary hypertension and related heart failure conditions. Its pipeline centers on levosimendan and imatinib, two repurposed drug candidates being advanced through clinical development.

Revenue0.0m USD
Operating profit (EBIT)-56.4m USD
−189.2 %y/y
Net income-52.6m USD
−198.8 %y/y
Free cash flow-35.8m USD
−141.7 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-60-40-20020m USD2020: EBIT 9.9 m USD20202021: EBIT -33 m USD20212022: EBIT 11 m USD20222023: EBIT -8.2 m USD20232024: 0.00 m USD2024: EBIT -19 m USD20242025: 0.00 m USD2025: EBIT -56 m USD20250.00-56
RevenueOperating profit (EBIT)

Business

Share of revenue
Levosimendan development50 %

Clinical development of levosimendan as a therapy for pulmonary hypertension and related cardiopulmonary disease.

Imatinib development30 %

Clinical development of imatinib for pulmonary arterial hypertension and other potential indications.

Clinical trial operations20 %

Execution of preclinical work and clinical studies needed to advance product candidates.

Customers

Tenax Therapeutics does not sell commercial medicines today; its primary stakeholders are clinical trial participants, investigators, and research sites that support development programs. If approved, its eventual customers would be physicians, hospitals, and specialty treatment centers serving patients with pulmonary hypertension and heart failure-related cardiopulmonary disease.

Clinical trial sites and investigators

They enroll patients, run studies, and generate the clinical evidence needed for regulatory approval.

Pulmonary hypertension specialists

They shape trial design and would be the main prescribers if the therapies are approved.

Hospitals and specialty care centers

They would administer or prescribe approved cardiopulmonary therapies in advanced disease settings.

Patients with pulmonary hypertension

The target patient population for levosimendan and imatinib development programs.

Strategy

The company is prioritizing levosimendan while continuing to evaluate imatinib as a longer-term program for pulmonary arterial hypertension. Its strategy is to use repurposed drugs with established safety histories to reduce development risk and focus capital on late-stage clinical evidence generation.

Advance levosimendan through late-stage clinical developmentShort term

This is the lead asset and the main path to potential regulatory and commercial value.

Maintain optionality on imatinibMedium term

Imatinib provides a second cardiopulmonary program that could broaden the pipeline if development is successful.

Secure funding for multi-year developmentShort term

Clinical-stage drug development requires substantial capital before any product revenue is available.

Geography

Tenax Therapeutics is headquartered in the United States and conducts its development activities through U.S.-based corporate operations and clinical programs. Its business is geographically tied to where clinical trials are run and where future regulatory approvals and commercialization would occur, with the U.S. being the core operating base.

Risks

Tenax faces the core risks of clinical-stage drug development: trial enrollment uncertainty, clinical failure, regulatory delay, and the possibility that additional capital will be needed before commercialization. Because its value depends on a small number of product candidates, setbacks in levosimendan or imatinib could materially affect the business.

Sorted by severity
Clinical development riskCritical

The company depends on successful trial outcomes for levosimendan and imatinib.

Exposure: Levosimendan and imatinib programs

Patient enrollment riskHigh

Trial timelines depend on recruiting eligible pulmonary hypertension patients.

Exposure: LEVEL trial and future Phase 3 studies

Financing riskHigh

The company may need additional capital to complete development and commercialization.

Exposure: Operating runway and future trial funding

Regulatory riskHigh

FDA approval requires positive clinical evidence and acceptable safety/efficacy data.

Exposure: All product candidates

Pipeline concentrationHigh

A small number of programs means one setback can disproportionately affect valuation.

Exposure: Levosimendan and imatinib

Accounting

Judgemental items
Clinical trial accruals

Trial costs are recognized as services are received, requiring estimates for CRO and site obligations.

Impact: Affects R&D expense and liabilities

Stock-based compensation

Equity awards are a meaningful compensation tool for a development-stage company.

Impact: Affects operating expenses and equity dilution

Warrants and financing instruments

Recent offerings included pre-funded warrants and warrants that may require careful classification and valuation.

Impact: Affects equity, liabilities, and financing-related gains or losses

Cash and investment valuation

Excess cash is invested in money market instruments and high-quality bonds, which must be measured appropriately.

Impact: Affects interest income and balance sheet presentation

Publicly listed companies with a comparable business focus.

Last updated: 29/04/2026