Cardiff Oncology (NASDAQ: CRDF) details Q1 2026 loss and Phase 3 plans
Rhea-AI Filing Summary
Cardiff Oncology reported first quarter 2026 results and a major clinical and leadership update. The company posted a net loss attributable to common stockholders of $12.4 million, or $0.18 per share, compared with a loss of $13.4 million, or $0.20 per share, a year earlier. Total operating expenses fell to $12.9 million from $14.5 million as research and development spending declined, partly offset by higher selling, general and administrative costs tied to severance and stock‑based compensation. Cash, cash equivalents and short‑term investments totaled $46.1 million as of March 31, 2026, and the company expects this to fund operations into the first quarter of 2027.
Clinically, Cardiff highlighted positive randomized Phase 2 CRDF‑004 data in first‑line RAS‑mutated metastatic colorectal cancer, where the 30 mg onvansertib plus FOLFIRI/bevacizumab arm achieved a confirmed objective response rate of 72.2% versus 43.2% across combined standard‑of‑care arms and showed improved progression‑free survival (hazard ratios 0.38 and 0.37, p<0.05) without significant added toxicity. Following a successful End‑of‑Phase 2 FDA meeting, the company selected a 30 mg onvansertib dose with FOLFIRI/bev for a planned Phase 3 registrational trial and plans to share more details by mid‑2026. Cardiff also announced that updated CRDF‑004 data will be presented in a rapid oral session at the 2026 ASCO Annual Meeting and that new preclinical data support combining onvansertib with an antibody‑drug conjugate in HER2‑low breast cancer models. Leadership was strengthened with Mani Mohindru appointed permanent CEO and new CFO and COO hires to support upcoming clinical and regulatory milestones.
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8-K Event Classification
Key Figures
Key Terms
End-of-Phase 2 meeting regulatory
Phase 3 registrational trial regulatory
objective response rate medical
progression-free survival medical
hazard ratio medical
antibody-drug conjugate medical
Earnings Snapshot
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On May 14, 2026, Cardiff Oncology, Inc. issued a press release announcing a business update and financial results for the first quarter ended March 31, 2026. A copy of the press release is furnished as Exhibit 99.1 to this Form 8-K.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
99.1 |
Press Release of Cardiff Oncology, Inc. dated May 14, 2026 |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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CARDIFF ONCOLOGY, INC. |
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Date: |
May 14, 2026 |
By: |
/s/ Mani Mohindru |
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Mani Mohindru |
Cardiff Oncology Reports First Quarter 2026 Results and Provides Business Update
Completed successful End-of-Phase 2 meeting with the FDA and selected onvansertib dose and chemotherapy regimen for planned Phase 3 trial
Company to provide detailed data update from Phase 2 CRDF-004 trial in rapid oral presentation at
American Society of Clinical Oncology Annual Meeting
Leadership additions position Company to execute on key upcoming clinical and regulatory milestones
SAN DIEGO, Calif., May 14, 2026 — Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinical-stage biotechnology company leveraging PLK1 inhibition to develop novel cancer therapies, today announced financial results for the first quarter ended March 31, 2026, and provided a business update.
"This quarter was marked by the positive data update from our randomized Phase 2 CRDF-004 trial of onvansertib in first-line RAS-mutated metastatic colorectal cancer, along with key leadership additions that prepare the Company to deliver on the clinical milestones ahead,” said Mani Mohindru, PhD, President and Chief Executive Officer of Cardiff Oncology.
“In April, we had a successful End‑of‑Phase 2 meeting with the FDA and aligned on the key design elements for our Phase 3 registrational trial. We plan to share additional Phase 3 details and our regulatory strategy in mid-2026. At the upcoming ASCO Annual Meeting, we will present updated CRDF-004 data, which we believe will provide further insight into onvansertib's potential in the first-line RAS-mutated metastatic colorectal cancer (mCRC) setting. In parallel, we continue to strengthen the scientific foundation of our PLK1 inhibition strategy, supported by new preclinical data evaluating combination use with an antibody-drug conjugate, as well as ongoing single-agent and combination investigator-initiated studies across multiple cancer settings. With strong clinical momentum, we remain focused on disciplined execution throughout the year.”
Clinical Highlights
Upcoming Event: Reporting Updated Onvansertib Data in Rapid Oral Presentation at American Society of Clinical Oncology (ASCO) Annual Meeting 2026
Completed End-of-Phase 2 Meeting with the FDA and Aligned on the Design of the Phase 3 Registrational Trial in Patients with First-line RAS-mutated mCRC
Key Opinion Leader Engagements Highlight Onvansertib Clinical Data and Opportunity in mCRC
Announced Positive Update from our Randomized Phase 2 Trial of Onvansertib in First-line RAS-mutated mCRC
Preclinical Highlights
Company Presented New Preclinical Data at the 2026 American Association for Cancer Research (AACR) Annual Meeting Supporting Rationale for Onvansertib in Combination with Antibody Drug Conjugates
Corporate Update
Key Leadership Appointments Strengthen Executive Team to Support Company’s Next Phase of Growth
First Quarter 2026 Financial Results
Liquidity, cash burn, and cash runway
As of March 31, 2026, Cardiff Oncology had approximately $46.1 million in cash, cash equivalents, and short-term investments.
Net cash used in operating activities for the first quarter of 2026 was approximately $12.3 million, a decrease of approximately $0.5 million from $12.8 million for the same period in 2025.
Based on its current expectations and projections, the Company believes its current cash resources are sufficient to fund its operations into the first quarter of 2027.
Operating results
Total operating expenses were approximately $12.9 million for the three months ended March 31, 2026, a decrease of $1.6 million from $14.5 million for the same period in 2025. The decrease in operating expenses was primarily due to a decrease of $3.7 million in R&D expenses, mainly clinical trial expenses and preclinical activities, partially offset by an increase of $2.1 million in SG&A expenses, primarily for employee severance agreements and corresponding modifications of stock options.
About Cardiff Oncology, Inc.
Cardiff Oncology is a clinical-stage biotechnology company advancing innovative cancer treatments focused on PLK1 inhibition, a validated oncology target with practice-changing potential. Our lead asset, onvansertib, is a highly specific, oral PLK1 inhibitor currently being evaluated in a Phase 2 trial for first-line treatment of RAS-mutated metastatic colorectal cancer (mCRC), addressing a large, underserved patient population with high unmet need. Onvansertib is also under investigation in other PLK1-driven cancers through ongoing investigator-initiated trials and has shown robust single agent clinical activity in hard-to-treat tumors. By targeting tumor vulnerabilities, we aim to overcome treatment resistance and deliver improved clinical outcomes for patients.
For more information, please visit https://www.cardiffoncology.com.
Forward-Looking Statements
Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified using words such as "anticipate," "believe," "forecast," "estimated" and "intend" or other similar terms or expressions that concern Cardiff Oncology's expectations, strategy, plans or intentions. These forward-looking statements are based on Cardiff Oncology's current expectations and actual results could differ materially. There are several factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, clinical trials involve a lengthy and expensive process with an uncertain outcome, and results of earlier studies and trials may not be predictive of future trial results; our clinical trials may be suspended or discontinued due to unexpected side effects or other safety risks that could preclude approval of our product candidate; results of preclinical studies or clinical trials for our product candidate could be unfavorable or delayed; our need for additional financing; risks related to business interruptions, including the outbreak of COVID-19 coronavirus and cyber-attacks on our information technology infrastructure, which could seriously harm our financial condition and increase our costs and expenses; uncertainties of government or third party payer reimbursement; dependence on key personnel; limited experience in marketing and sales; substantial competition; uncertainties of patent protection and litigation; dependence upon third parties; and risks related to failure to obtain FDA clearances or approvals and noncompliance with FDA regulations. There are no guarantees that our product candidate will be utilized or prove to be commercially successful. Additionally, there are no guarantees that future clinical trials will be completed or successful or that our product candidate will receive regulatory approval for any indication or prove to be commercially successful. Investors should read the risk factors set forth in Cardiff Oncology's Form 10-K for the year ended December 31, 2025, and other periodic reports filed with the Securities and Exchange Commission. While the list of factors presented here is considered representative, no such list should be considered to be a complete statement of all potential risks and uncertainties. Unlisted factors may present significant additional obstacles to the realization of forward-looking statements. Forward-looking statements included herein are made as of the date hereof, and Cardiff Oncology does not undertake any obligation to update publicly such statements to reflect subsequent events or circumstances.
Investor Contact:
Candice Masse
astr partners
candice.masse@astrpartners.com
Media Contact:
Amy Bonanno
Lyra Strategic Advisory
abonanno@lyraadvisory.com
Cardiff Oncology, Inc.
Condensed Statements of Operations
(in thousands, except for per share amounts)
(unaudited)
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Three Months Ended March 31, |
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2026 |
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2025 |
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Royalty revenues |
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$ |
41 |
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$ |
109 |
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Costs and expenses: |
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Research and development |
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6,765 |
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10,477 |
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Selling, general and administrative |
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6,126 |
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4,014 |
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Total operating expenses |
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12,891 |
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14,491 |
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Loss from operations |
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(12,850 |
) |
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(14,382 |
) |
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Other income (expense), net: |
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Interest income |
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506 |
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941 |
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Other income (expense), net |
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(1 |
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7 |
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Total other income (expense), net |
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505 |
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948 |
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Net loss |
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(12,345 |
) |
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(13,434 |
) |
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Preferred stock dividend |
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(6 |
) |
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(6 |
) |
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Net loss attributable to common stockholders |
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$ |
(12,351 |
) |
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$ |
(13,440 |
) |
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Net loss per common share — basic and diluted |
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$ |
(0.18 |
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$ |
(0.20 |
) |
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Weighted-average shares outstanding — basic |
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68,350 |
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66,524 |
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Cardiff Oncology, Inc.
Condensed Balance Sheets
(in thousands)
(unaudited)
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March 31, |
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December 31, |
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Assets |
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Current assets: |
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Cash and cash equivalents |
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$ |
8,544 |
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$ |
17,470 |
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Short-term investments |
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37,512 |
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40,834 |
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Accounts receivable and unbilled receivable |
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191 |
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182 |
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Prepaid expenses and other current assets |
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1,095 |
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1,642 |
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Total current assets |
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47,342 |
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60,128 |
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Property and equipment, net |
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491 |
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578 |
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Operating lease right-of-use assets |
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495 |
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629 |
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Other assets |
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844 |
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549 |
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Total Assets |
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$ |
49,172 |
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$ |
61,884 |
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Liabilities and Stockholders’ Equity |
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Current liabilities: |
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Accounts payable |
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$ |
5,480 |
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$ |
8,087 |
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Accrued liabilities |
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8,337 |
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7,577 |
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Operating lease liabilities |
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646 |
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730 |
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Total current liabilities |
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14,463 |
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16,394 |
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Operating lease liabilities, net of current portion |
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— |
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102 |
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Total Liabilities |
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14,463 |
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16,496 |
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Stockholders’ equity |
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34,709 |
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45,388 |
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Total liabilities and stockholders’ equity |
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$ |
49,172 |
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$ |
61,884 |
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