Corvus Pharmaceuticals (CRVS) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
6 Aug, 2026Executive summary
Focused on advancing soquelitinib, a first-in-class selective ITK inhibitor, across multiple indications including PTCL, atopic dermatitis, hidradenitis suppurativa, asthma, and ALPS, with Phase 3 and Phase 2 trials ongoing and additional studies planned.
Pipeline also includes ciforadenant (A2A receptor antagonist) and mupadolimab (anti-CD73 antibody), both in clinical development.
Strategic collaboration with Angel Pharmaceuticals in China to accelerate development and expand data sets, including parallel and new trials.
No product revenue to date; operations funded primarily through equity offerings and warrant exercises.
Financial highlights
R&D expenses for Q2 2026 were $16 million, up from $7.9 million in Q2 2025, mainly due to increased clinical trial and personnel costs.
Net loss for Q2 2026 was $18 million, compared to $8 million in Q2 2025; six-month net loss was $31.7 million, with prior year including $27.1 million non-operating income.
Cash, cash equivalents, and marketable securities totaled $215.2 million as of June 30, 2026, including $189.4 million in net proceeds from a Q1 follow-on offering.
Stock compensation expense for Q2 2026 was $2.6 million, up from $1.3 million in Q2 2025.
Accumulated deficit reached $443.9 million as of June 30, 2026.
Outlook and guidance
Cash position expected to fund operations into Q2 2028; additional capital will be needed for full development and commercialization.
Anticipated completion of enrollment for the phase II atopic dermatitis trial in early 2027, with top-line data in Q3 2027.
Interim futility analysis for the phase III PTCL trial expected in Q1 2027; final data projected for late 2027.
Planned initiation of phase II asthma and phase Ib hidradenitis suppurativa trials before year-end 2026.
Results from Angel Pharma’s Phase 1b atopic dermatitis trial anticipated late 2026; Phase 2 asthma trial in China expected to initiate in early 2027.
Latest events from Corvus Pharmaceuticals
- Soquelitinib shows robust efficacy and safety in AD, supporting broad immune disease potential.CRVS
Corporate presentation6 Aug 2026 - Soquelitinib showed robust efficacy and safety, with $31.3M raised to fund operations into late 2026.CRVS
Q1 20259 Jul 2026 - Strong efficacy, safety, and immune modulation support Phase II trials for soquelitinib in atopic dermatitis.CRVS
Study result9 Jul 2026 - Soquelitinib advances with strong clinical data and a $52M cash runway into Q1 2026.CRVS
Q4 20248 Jul 2026 - Lead asset soquelitinib advances in oncology and immunology with strong IP and cash runway.CRVS
Goldman Sachs 47th Annual Global Healthcare Conference 20268 Jun 2026 - Durable efficacy and safety demonstrated in immune diseases, with broad clinical expansion underway.CRVS
Jefferies Global Healthcare Conference 20263 Jun 2026 - Soquelitinib achieved durable efficacy, safety, and immune rebalancing in atopic dermatitis.CRVS
Study update20 May 2026 - Q1 2026 net loss of $13.7M, $236.7M cash, clinical advances, runway into Q2 2028.CRVS
Q1 20267 May 2026 - Virtual annual meeting to vote on directors, auditor ratification, and executive pay.CRVS
Proxy filing24 Apr 2026