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Corvus Pharmaceuticals (CRVS) investor relations material
Corvus Pharmaceuticals Q3 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Soquelitinib Phase 3 relapsed/refractory PTCL and Phase 2 atopic dermatitis trials remained on track; development is also expanding into hidradenitis suppurativa, asthma and ALPS.
Cash, cash equivalents and marketable securities totaled $202.9M at September 30, 2026, and were expected to fund operations into Q2 2028.
No product sales revenue has been generated.
Financial highlights
Q3 2026 R&D expense was $17.8M vs. $8.5M in Q3 2025, reflecting higher soquelitinib trial and personnel costs.
Q3 2026 net loss was $20.3M vs. $10.2M; nine-month net loss was $52.0M vs. $3.0M, with the prior-year period including a $27.1M warrant fair-value gain.
Q3 operating expenses were $21.4M vs. $10.6M YoY; nine-month expenses were $55.5M vs. $30.8M.
Q3 G&A was $3.6M vs. $2.1M; nine-month G&A was $10.6M vs. $7.0M, primarily due to personnel and outside-service costs.
Q3 stock-based compensation was $2.8M vs. $1.2M; nine-month expense was $8.1M vs. $3.8M.
Outlook and guidance
PTCL Phase 3 futility analysis is expected in Q1 2027; trial data are anticipated in late 2027/early 2028.
SIERRA1 atopic dermatitis top-line data are anticipated in Q3 2027; a Phase 3 trial could start in 2028 if results support advancement.
Hidradenitis suppurativa Phase 1b data are targeted for H1 2027; asthma Phase 2 initiation is expected in Q1 2027.
Angel atopic dermatitis cohort 1 preliminary results are expected in March 2027, with cohort 2 data potentially in H2 2027; Angel asthma Phase 2 initiation is anticipated in Q2 2027.
R&D and G&A spending are expected to increase as clinical development advances; additional capital will be needed to fund programs through commercialization.
- Oral ITK inhibitor soquelitinib targets multiple immune diseases with pivotal data expected by 2027.CRVS
12th Annual Cantor Fitzgerald Global Healthcare Conference - Soquelitinib shows robust efficacy and safety in AD, supporting broad immune disease potential.CRVS
Corporate presentation - Q2 2026 net loss rose to $18M as R&D spending increased; cash runway extends into Q2 2028.CRVS
Q2 2026 - Lead asset soquelitinib advances in oncology and immunology with strong IP and cash runway.CRVS
Goldman Sachs 47th Annual Global Healthcare Conference 2026 - Durable efficacy and safety demonstrated in immune diseases, with broad clinical expansion underway.CRVS
Jefferies Global Healthcare Conference 2026 - Soquelitinib achieved durable efficacy, safety, and immune rebalancing in atopic dermatitis.CRVS
Study update - Strong efficacy, safety, and immune modulation support Phase II trials for soquelitinib in atopic dermatitis.CRVS
Study result - Soquelitinib showed robust efficacy and safety, with $31.3M raised to fund operations into late 2026.CRVS
Q1 2025 - Soquelitinib advances with strong clinical data and a $52M cash runway into Q1 2026.CRVS
Q4 2024
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