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Veru (VERU) investor relations material
Veru Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Focus on late-stage clinical development of enobosarm for obesity and muscle preservation in older adults, and sabizabulin for atherosclerotic cardiovascular disease inflammation.
Positive phase II-B QUALITY trial results showed enobosarm, alone or with GLP-1 RAs, preserved lean mass and led to greater fat loss, with monotherapy preventing weight regain after semaglutide discontinuation.
Strategic shift completed with the sale of the FC2 Female Condom business in December 2024; all prior product revenues now classified as discontinued operations.
No commercial revenue in the current quarter; all revenues, costs, and expenses from discontinued operations.
Phase 2b PLATEAU clinical trial for enobosarm plus semaglutide in older obese patients to begin in Q1 2026, with interim analysis expected in Q1 2027.
Financial highlights
Net loss for the quarter was $5.3 million ($0.26 per diluted share), improved from $8.9 million ($0.61 per share) in the prior year.
Research and development expenses decreased to $1.3 million from $5.7 million year-over-year, mainly due to the completion of the QUALITY study.
General and administrative expenses fell to $4.1 million from $5.2 million, primarily due to lower share-based compensation.
Cash, cash equivalents, and restricted cash totaled $33.0 million as of December 31, 2025, up from $15.8 million at September 30, 2025.
Net working capital increased to $29.7 million from $11.1 million sequentially.
Outlook and guidance
Cash on hand is expected to fund operations through the interim analysis of the phase II-B PLATEAU study, with trial initiation in Q1 2026 and interim analysis in Q1 2027.
FDA feedback provides two regulatory pathways for enobosarm/GLP-1 RA combination approval: incremental weight loss or preservation of physical function.
Expects to continue incurring significant expenses and operating losses as drug candidates advance.
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