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Mink Therapeutics (INKT) investor relations material
Mink Therapeutics Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Advanced randomized phase II trial of agenT-797 for acute lung injury and ARDS, with initial dosing in Ukraine and U.S. site activation underway; early data showed improved survival, oxygenation, and no major serious adverse events.
Launched international paid named patient access program in Brazil, expanding access and generating program revenue.
Expanded operational infrastructure for global delivery of off-the-shelf cell therapy, supporting clinical trials and responsible access.
Focused on developing allogeneic, off-the-shelf iNKT cell therapies for cancer and immune-mediated diseases, with a pipeline including native and engineered iNKT therapies.
Collaborations and investigator-sponsored trials are expanding access and generating non-promotional revenue.
Financial highlights
Ended Q2 2026 with $8.8 million in cash and equivalents, down from $13.4 million at year-end 2025.
Net loss for Q2 2026 was $3.1 million ($0.62/share), improved from $4.2 million ($1.06/share) in Q2 2025.
Net loss for the first six months of 2026 was $5.9 million ($1.20/share), compared to $7.0 million ($1.76/share) for the same period last year.
Cash used in operations for the first half of 2026 was $3.8 million, up from $2.9 million in the prior year.
Accumulated deficit reached $162.5 million as of June 30, 2026.
Outlook and guidance
Enrollment in the phase II ARDS trial continues in Ukraine, with U.S. sites to begin enrolling in September; preliminary randomized data expected in early 2027.
Plans to seek FDA meeting to transition from phase II to a seamless phase III study.
Anticipates expanding the named patient access program to additional regions as regulatory approvals are obtained.
Management expects continued operating losses and negative cash flows until commercialization or substantial partnering.
Cash and anticipated funding expected to cover liquidity needs for more than one year, but substantial doubt exists about ability to continue as a going concern.
- Directors and auditor elected, immune restoration strategy advanced, and global trials expanded.INKT
AGM 2026 - Advanced iNKT cell therapy into Phase II trials, expanded platform, and maintained $9.5M cash.INKT
Q1 2026 - Director elections, auditor ratification, and governance oversight headline the annual meeting.INKT
Proxy filing - Durable clinical results, strong cash position, and major trial milestones expected in 2026.INKT
Q4 2025 - Net loss narrowed, cash burn fell, and clinical progress continues amid funding risks.INKT
Q3 2024 - iNKT cell therapies show promise in hard-to-treat cancers and ARDS, with pivotal trials underway.INKT
H.C. Wainwright 26th Annual Global Investment Conference 2024 - Net loss narrowed, cash increased, and iNKT pipeline advanced, but funding risks remain.INKT
Q2 2024 - Clinical advances, reduced cash burn, and NIAID funding support growth amid liquidity risks.INKT
Q1 2025 - Net loss narrowed, cash burn fell, and clinical pipeline advanced toward 2025 milestones.INKT
Q4 2024
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