Welcome to our dedicated page for Corvus Pharmaceu news (Ticker: CRVS), a resource for investors and traders seeking the latest updates and insights on Corvus Pharmaceu stock.
Corvus Pharmaceuticals (CRVS) is a clinical-stage biopharmaceutical company advancing novel immunotherapies targeting T cell modulation through ITK inhibition. This page provides investors and industry stakeholders with timely updates on CRVS’s clinical developments, regulatory milestones, and strategic initiatives.
Access the latest press releases, earnings reports, and research updates in one centralized location. Track progress across the company’s pipeline, including soquelitinib for T cell lymphomas and autoimmune conditions, as well as collaborations shaping its therapeutic platform.
Key updates include clinical trial results, partnership announcements, and financial performance. Bookmark this page to stay informed about CRVS’s advancements in immuno-oncology and immune-mediated disease research. Visit regularly for authoritative insights into the company’s scientific and operational progress.
Corvus Pharmaceuticals (NASDAQ: CRVS) provided a business update and reported Q3 2025 results on Nov 4, 2025. Key clinical milestones include completed enrollment in the soquelitinib atopic dermatitis Phase 1 extension cohort 4 with data anticipated in Jan 2026, a Phase 2 atopic dermatitis trial on track to start in early Q1 2026 (≈200 patients), and an ongoing registrational Phase 3 in relapsed/refractory PTCL (target ≈150 patients) with final Phase 1/1b data to be presented orally at ASH Dec 2025.
Financials: cash, cash equivalents and marketable securities of $65.7M as of Sept 30, 2025, expected to fund operations into Q4 2026. R&D expense for Q3 2025 was $8.5M vs $5.2M year-ago; net loss was $10.2M for the quarter.
Corvus Pharmaceuticals (NASDAQ: CRVS) will present final data from its Phase 1/1b trial of soquelitinib in relapsed/refractory T cell lymphomas at the 67th American Society of Hematology Annual Meeting & Exposition.
The oral presentation is scheduled for December 8, 2025, Session 625 (T Cell, NK Cell, or NK/T Cell Lymphomas), with a presentation slot from 11:15 AM–11:30 AM (session 10:30 AM–12:00 PM). Publication number is 778; the title reports final Phase 1 results for soquelitinib (SQL), an ITK inhibitor for R/R T cell lymphomas.
Corvus Pharmaceuticals (NASDAQ: CRVS) announced that its leadership team will hold one-on-one investor meetings and deliver a fireside chat at the Guggenheim 2nd Annual Healthcare Innovation Conference in Boston.
The fireside chat is scheduled for Monday, November 10, 2025 at 8:30 AM ET. A live webcast will be available and archived for 90 days via the company’s investor relations website.
Corvus Pharmaceuticals (NASDAQ: CRVS) will provide a business update and report third quarter 2025 financial results on November 4, 2025. The company will host a conference call and live webcast at 4:30 pm ET / 1:30 pm PT. Participants can dial 1-800-717-1738 (toll-free U.S.) or 1-646-307-1865 (international), or join via the instant telephone access link and the company’s investor relations webcast page. A replay of the webcast will be available on the Corvus website for 90 days.
Corvus Pharmaceuticals (Nasdaq: CRVS) announced interim Phase 1b/2 data (data cutoff May 2025) for ciforadenant combined with ipilimumab and nivolumab in first-line metastatic renal cell carcinoma presented at ESMO 2025 on October 17, 2025.
Key points: the open-label trial enrolled 50 patients, showed the triplet was feasible and well tolerated, deep response rate 34% versus ~32% historical doublet rate, objective response rate 46% (2 CR, 21 PR), median PFS 11.04 months, and 19 patients remain on therapy for longer follow-up.
Corvus Pharmaceuticals (NASDAQ: CRVS) announced on October 2, 2025 the appointment of David Moore to its Board of Directors. Mr. Moore is Executive Vice President, US Operations and President at Novo Nordisk Inc., with 27 years of industry experience across strategy, commercial, market access, business development and private equity. Management expects his commercial and corporate development experience to support advancement of Corvus’ ITK inhibitor pipeline.
Corvus Pharmaceuticals (NASDAQ:CRVS) reported significant progress in its clinical trials and financial results for Q2 2025. The company's lead drug candidate soquelitinib showed promising results in Phase 1 trials for atopic dermatitis, with cohort 3 achieving a 64.8% mean EASI reduction compared to 34.4% for placebo. The company is advancing multiple clinical programs, including a Phase 3 trial for peripheral T cell lymphoma (PTCL) and collaboration with NIAID for ALPS treatment.
Financially, Corvus strengthened its position with warrant exercises providing $35.7 million in proceeds during Q2, ending the quarter with $74.4 million in cash. The company expects its cash runway to extend into Q4 2026. R&D expenses increased to $7.9 million, up from $4.1 million in Q2 2024, with a net loss of $8.0 million.
Corvus Pharmaceuticals (NASDAQ: CRVS), a clinical-stage biopharmaceutical company, has scheduled its second quarter 2025 financial results and business update conference call for August 7, 2025 at 4:30 pm ET.
Investors can access the call via telephone at 1-800-717-1738 (domestic) or 1-646-307-1865 (international). A live webcast will be available through the company's investor relations website, with a replay accessible for 90 days following the presentation.
Corvus Pharmaceuticals (NASDAQ: CRVS) announced that its Chinese partner Angel Pharmaceuticals received IND approval from China's NMPA to begin a Phase 1b/2 clinical trial of soquelitinib for treating moderate-to-severe atopic dermatitis.
The trial will evaluate 12-week dosing across multiple cohorts, with Phase 1b enrolling 48 patients across two cohorts testing different dosing regimens. Patient enrollment is expected to begin in Q3 2025, with Phase 1b data anticipated in 2026. The study will be led by Dr. Yuling Shi, a prominent dermatology expert from Shanghai Skin Disease Hospital.
Corvus, which co-founded Angel Pharma to develop its pipeline in greater China, has licensed the rights for soquelitinib development, manufacturing, and commercialization in the region to Angel Pharma.