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8-K2026-05-07· grok-4-1-fast-non-reasoning

CRVS · Corvus Pharmaceuticals, Inc.

0001171843-26-003154

SEC filing

Summary

Corvus Pharmaceuticals reported Q1 2026 financial results with $236.7 million in cash supporting operations into Q2 2028, alongside positive Phase 1 soquelitinib data and Phase 2 trial initiations in atopic dermatitis.

Key takeaways

Full analysis

Corvus Pharmaceuticals disclosed its first quarter 2026 financial results and business update via press release on May 7, 2026. The company reported a net loss of $13.7 million, compared to net income of $15.2 million in the prior year period, primarily driven by higher research and development expenses of $11.2 million versus $7.5 million, attributed to increased clinical trial costs for soquelitinib and personnel-related expenses. Stock-based compensation rose to $2.7 million from $1.3 million. Balance sheet strengthened significantly with cash, cash equivalents, and marketable securities at $236.7 million as of March 31, 2026, including $189.4 million net proceeds from a January 23, 2026 financing, up from $56.8 million at December 31, 2025. This cash position funds operations into Q2 2028. CEO Richard A. Miller highlighted strong momentum for soquelitinib, a selective ITK inhibitor, positioning it for atopic dermatitis, immune diseases, and cancers through immune system rebalancing. Key clinical progress includes positive Phase 1 cohort 4 data in moderate-to-severe atopic dermatitis (as of January 15, 2026), with final data and new immunologic/biomarker insights on drug-free remission potential to be presented at the Society for Investigative Dermatology annual meeting May 13-16, 2026 in Chicago. An investor meeting is set for May 14, 2026. The company initiated a Phase 2 atopic dermatitis trial in Q1 2026, targeting 200 patients across doses with 12-week treatment and 90-day follow-up. Angel Pharmaceuticals is enrolling a Phase 1b/2 trial in China with similar design, results expected late 2026. Upcoming Phase 2 trials in hidradenitis suppurativa and asthma are planned later 2026. In oncology, Phase 3 registrational trial in relapsed/refractory PTCL (NCT06561048) continues enrolling toward 150 patients versus belinostat or pralatrexate, with PFS primary endpoint; soquelitinib holds Orphan Drug and Fast Track designations. NIAID-collaborated ALPS Phase 2 trial (NCT06730126) advances, targeting 30 patients.