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Tenax Therapeutics Q2 2026: $17.8M Net Loss, $118M Cash, LEVEL Data Due August

$118.0 million in cash and cash equivalents sat on Tenax Therapeutics' (Nasdaq: TENX) balance sheet at June 30, 2026, up from $97.6 million at December 31, 2025, with $13.4 million of the gain from warrant exercises during the quarter…

By Ines Ferreira·Jul 31, 2026·2 min read·regulatory·TENX

Key takeaways

  • Tenax Therapeutics reported a Q2 2026 net loss of $17.8 million, up from $10.9 million in Q2 2025.
  • The company held $118.0 million in cash and cash equivalents as of June 30, 2026, versus $97.6 million at December 31, 2025.
  • Topline data from the Phase 3 LEVEL trial of TNX-103 (oral levosimendan) in PH-HFpEF is expected in August 2026.
  • R&D expenses reached $12.9 million in Q2 2026, up from $6.1 million a year earlier, driven by the concurrent LEVEL and LEVEL-2 Phase 3 trials.
  • Tenax guides its cash runway through Q2 2028.

$118.0 million in cash and cash equivalents sat on Tenax Therapeutics' (Nasdaq: TENX) balance sheet at June 30, 2026, up from $97.6 million at December 31, 2025, with $13.4 million of the gain from warrant exercises during the quarter. Tenax reported a net loss of $17.8 million for Q2 2026, against $10.9 million in Q2 2025, as R&D expenses nearly doubled YoY. The company now guides cash runway through Q2 2028 and expects topline data from its Phase 3 LEVEL trial in August 2026.

R&D nearly doubles as two Phase 3 trials run concurrently

R&D expenses reached $12.9 million in Q2 2026, up from $6.1 million in Q2 2025, a $6.8 million YoY increase. The driver: LEVEL and LEVEL-2, two double-blind, randomized, placebo-controlled Phase 3 trials of TNX-103 (oral levosimendan) in pulmonary hypertension associated with heart failure with preserved ejection fraction (PH-HFpEF), running in parallel. LEVEL-2 began in December 2025; enrollment is projected to complete by end of 2027.

SG&A was $5.9 million versus $5.7 million a year earlier. Higher legal and professional fees and personnel costs drove the increase, partially offset by lower stock-based compensation. Combined Q2 operating expenses: $18.8 million.

LEVEL readout and ESC Congress, August 28-31

An abstract has been submitted and accepted for a Late-Breaking Clinical Science session at the European Society of Cardiology Congress 2026 in Munich, Germany, scheduled August 28-31. Topline LEVEL data is expected in time for that presentation. Chris Giordano, President and CEO, described Tenax as approaching a moment the company has been preparing for since it began developing a therapy for PH-HFpEF, an indication for which no product has been approved. Levosimendan carries market authorization in 60 countries in an intravenous formulation for hospitalized heart failure patients, though it remains unavailable in the United States or Canada.

Balance sheet snapshot

Item June 30, 2026 Dec 31, 2025
Cash and equivalents $118.0M $97.6M
Total assets $121.7M $104.2M
Total current liabilities $8.1M $7.2M
Additional paid-in capital $514.6M $464.5M
Accumulated deficit ($401.0M) ($367.5M)
Stockholders' equity $113.6M $97.1M
Shares outstanding 31,949,785 9,314,130

Shares outstanding expanded 3.4x from year-end 2025, with additional paid-in capital rising $50.1 million over the same six months. Accumulated deficit widened $33.5 million in the period, reaching $401.0 million.

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Source: sec.gov
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Frequently asked

When will Tenax report the LEVEL trial data?

Topline LEVEL data is expected in August 2026, in time for a Late-Breaking Clinical Science presentation at the European Society of Cardiology Congress 2026 in Munich, scheduled August 28-31.

What condition is TNX-103 being developed to treat?

TNX-103 (oral levosimendan) is being developed for pulmonary hypertension associated with heart failure with preserved ejection fraction (PH-HFpEF), an indication for which no product has been approved.

Why did Tenax's R&D expenses increase so much year over year?

R&D nearly doubled to $12.9 million because the company is running two Phase 3 trials, LEVEL and LEVEL-2, in parallel, with LEVEL-2 having begun in December 2025.

How did Tenax's cash position increase during the quarter?

Cash rose to $118.0 million partly due to $13.4 million from warrant exercises during the quarter, and shares outstanding expanded 3.4x from year-end 2025.

Is levosimendan already approved anywhere?

Levosimendan carries market authorization in 60 countries in an intravenous formulation for hospitalized heart failure patients, but it remains unavailable in the United States and Canada.