Extended Cash Runway and Strong Year‑End Cash Balance
Cash runway extended into 2029 (assuming no further cash inflows) via a non‑dilutive transaction with AstraZeneca. Year‑end cash, cash equivalents, short‑term deposits and marketable securities totaled approximately $145.6M, which includes the $65.0M upfront payment from AstraZeneca.
Substantial Revenue Increase Driven by Partner Upfronts
Reported revenue for quarter ended 12/31/2025 of ~$67.3M vs ~$1.5M in the comparable quarter of 2024 (~+4,387%), and revenue for the year ended 12/31/2025 of ~$72.8M vs ~$27.9M in 2024 (~+161%). 2025 revenues included the $65.0M AstraZeneca upfront and components of the Gilead upfront/IND milestone.
Swing to Profitability
Quarter ended 12/31/2025 net profit of ~$56.8M (~$0.60 per basic and diluted share) vs a net loss of ~$6.1M (~$0.07 per share loss) in the comparable quarter of 2024. Full‑year 2025 net profit of ~$35.3M (~$0.38 per share) vs a net loss of ~$14.2M (~$0.16 per share) in 2024—driven primarily by non‑recurring partner payments.
Clinical Advancement of COM701 (Ovarian Program)
Initiated dosing in the MAIA adaptive randomized maintenance trial of COM701 in platinum‑sensitive ovarian cancer and expanded trial footprint globally; 28 sites are now open across the U.S., Israel and France. Pooled Phase I data in platinum‑resistant ovarian cancer presented at ESMO showed COM701 was well tolerated with consistent durable responses in heavily pretreated patients, especially those without liver metastases, supporting exploration in earlier‑line maintenance settings.
Progress on GS‑0321 and Partner Funding
GS‑0321 (anti–IL‑18BP antibody) entered Phase I dose‑escalation/expansion (first patient dosed January 2025) and received scientific presentation at SITC. Gilead paid €60.0M upfront plus $30.0M on IND clearance; Compugen is eligible for up to an additional $758.0M in future milestones plus tiered royalties (single‑digit to low double‑digit).
Partnership Validation and Upside from Rilvegostomig
Strategic relationship with AstraZeneca validated by a monetization transaction and continued broad late‑stage development of rilvegostomig (AstraZeneca running ~10–11 active Phase III trials). Company retained majority of royalty interest and remains eligible for mid‑single‑digit tiered royalties; AstraZeneca previously estimated non‑risk‑adjusted peak annual revenue potential for rilvegostomig above $5.0B.
Controlled Operating Expenses
R&D expenses decreased to ~$5.5M for the quarter (vs ~$5.9M prior year quarter, approx. -6.8%) and ~$22.8M for the year (vs ~$24.8M prior year, approx. -8.1%). G&A expenses also declined modestly to ~$2.1M for the quarter (vs ~$2.2M, approx. -4.5%) and ~$8.9M for the year (vs ~$9.4M, approx. -5.3%), reflecting lower spend as prior trials wound down while selectively funding MAIA and early‑stage programs.