10-K annual report · filed Mar 12, 2026

Corvus Pharmaceuticals, Inc. (CRVS) FY2025 10-K Annual Report

Short answer

Corvus Pharmaceuticals, Inc. (CRVS) filed its fiscal 2025 10-K annual report with the SEC on Mar 12, 2026.

  • Top risk flagged: Regulatory risk FDA approval delay for soquelitinib with $21.2M R&D spend in 2025, clinical trial costs up $6.0M YoY

FY2025 key financial metrics · XBRL

Net income
−$15M
+75.5% YoY
EPS (diluted)
−$0.53
+48.0% YoY
ROE
-25.0%
+166.3 pp YoY
Operating cash flow
−$33M
−29.0% YoY

Source: XBRL data from the Corvus Pharmaceuticals, Inc. (CRVS) FY2025 10-K on SEC EDGAR. USD.

Corvus Pharmaceuticals, Inc. FY2025 10-K analysis

AI summary of each section, grounded in the filing text

Business Overview

  • Core business: Clinical-stage biopharma developing targeted immune cell protein inhibitors for immune-mediated diseases, inflammatory diseases, and cancers
  • New emphasis: Soquelitinib advanced to Phase 3 trial for relapsed peripheral T cell lymphoma (PTCL) and initiated Phase 2 trial for moderate-to-severe atopic dermatitis
  • Strategic shift: Expanded focus on immune and inflammatory diseases from oncology, demonstrated by ITK inhibitor’s novel mechanism rebalancing Th1/Th2/Th17/Treg cells
  • Quantitative highlight: Phase 1/1b trial enrolled 75 PTCL patients; Phase 1 atopic dermatitis trial enrolled 72 patients across 4 cohorts with up to 72% EASI score reduction
  • Noteworthy fact: FDA granted Fast Track and Orphan Drug designations for soquelitinib in relapsed PTCL; first clinical evidence of ITK inhibitor therapy efficacy in both cancer and inflammatory disease pathways

Management Discussion & Analysis

  • Forward-looking statements included but specifics on management outlook or guidance not given

Risk Factors

  • Regulatory risk FDA approval delay for soquelitinib with $21.2M R&D spend in 2025, clinical trial costs up $6.0M YoY
  • Macroeconomic risk accumulated deficit $412.3M with net loss $15.3M in 2025, cash runway only through Q2 2028
  • Operational risk manufacturing cost increase $4.8M for soquelitinib in 2025, reflecting supply chain cost pressures
  • Competitive risk dependence on clinical success of soquelitinib vs oncology market innovations, no approved products yet
  • Financial risk reliance on equity funding with $189.4M raised in January 2026 follow-on offering, ATM offering suspended

Generated from the filing text; verify against the original. How to read a 10-K

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