Cardiff Oncology (CRDF) Q3 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2026 earnings summary
12 Nov, 2026Executive summary
Q3 net loss narrowed year over year as R&D spending declined; $33.8M in cash, cash equivalents and short-term investments is projected to fund operations through Q3 2027.
The Phase 2 mCRC trial remains ongoing, with a registrational global Phase 3 trial of ~640 patients in preparation and potential initiation in Q1 2027.
Financial highlights
Q3 2026 royalty revenue was $171K vs. $120K; operating expenses were $9.4M vs. $12.1M, and net loss was $8.9M vs. $11.3M.
9M 2026 royalty revenue was $316K vs. $350K; operating expenses were $32.0M vs. $41.5M, and net loss was $30.4M vs. $38.6M.
Q3 R&D expense fell to $5.0M from $8.2M; SG&A rose to $4.4M from $3.9M, primarily due to NMS-related legal and professional fees.
9M R&D expense fell to $17.7M from $30.3M; SG&A rose to $14.3M from $11.2M, including legal fees and severance costs.
Interest income was $0.4M vs. $0.7M in Q3 and $1.3M vs. $2.5M for 9M.
Outlook and guidance
Current projections indicate capital resources fund operations through Q3 2027, but not for at least 12 months following issuance of the financial statements.
Planned CRDF-005 is a global randomized Phase 3 trial of onvansertib 30 mg plus FOLFIRI/bev vs. FOLFIRI/bev standard of care, targeting ~640 patients; potential start is Q1 2027.
EMA scientific advice is being sought on Phase 3 plans; clinical material manufacturing and companion diagnostic regulatory activities remain on track.
Additional CMML trial data are scheduled for presentation at the December 2026 ASH meeting.
Latest events from Cardiff Oncology
- A ~640-patient Phase III trial is planned for 1Q 2027, pending funding.CRDF
H.C. Wainwright 28th Annual Global Investment Conference - Vote to increase authorized shares aims to support future growth and financing flexibility.CRDF
Proxy filing - Shareholders will vote on a major increase in authorized shares at the October 2026 meeting.CRDF
Proxy filing - Vote sought to increase authorized shares and permit meeting adjournment if needed.CRDF
Proxy filing - Phase 2 success for onvansertib in mCRC; cash runway into Q3 2027, but litigation risk remains.CRDF
Q2 2026 - Onvansertib shows strong efficacy and safety in first-line RAS-mutated MCRC, with major updates due in Q1 2026.CRDF
Noble Capital Markets Emerging Growth Virtual Investor Conference - Advancing a well-tolerated PLK1 inhibitor to global phase III for RAS-mutated colorectal cancer.CRDF
Jefferies Global Healthcare Conference 2026 - 30 mg onvansertib plus FOLFIRI-BEV delivers 72.2% ORR and durable benefit in RAS-mutated mCRC.CRDF
Status update - Positive Phase 2 data, FDA alignment, and narrowed net loss offset by ongoing going concern risk.CRDF
Q1 2026