Cardiff Oncology Reports Third Quarter 2025 Results and Provides Business Update

Rhea-AI Summary

Cardiff Oncology (Nasdaq: CRDF) reported Q3 2025 results and a business update on Nov 6, 2025. The company announced positive Phase 2 CRDF-004 data for onvansertib plus standard of care in first-line RAS-mutated metastatic colorectal cancer, citing a 19% improvement in confirmed ORR for the 30mg cohort at the July 8, 2025 data cut-off and early PFS separation favoring 30mg.

Cardiff reported $60.6 million in cash and investments as of Sept 30, 2025, net cash used in operating activities of $10.8 million in Q3 2025, and projects runway into Q1 2027. A clinical update is expected in Q1 2026.

Positive

• ORR +19% in 30mg onvansertib arm vs control (intent-to-treat)
• $60.6M cash and short-term investments as of Sept 30, 2025
• Projected cash runway into Q1 2027
• Dose-dependent improvements across ORR, PFS, and tumor shrinkage

Negative

• Net cash used in operating activities of $10.8M in Q3 2025
• Operating expenses remain significant at $12.1M for Q3 2025
• Clinical results are early; median PFS not yet reached

Insights

Clinical-biotech analyst

Positive Phase 2 efficacy signal plus a multi-quarter cash runway; next data readout in Q1 2026 is the immediate catalyst.

Onvansertib showed a 19% improvement in confirmed ORR at the 30mg dose versus control and dose-dependent benefit across ORR, PFS trends, early tumor shrinkage, and depth of response. The program reports no major or unexpected toxicities and the company plans a clinical update in Q1 2026. These are concrete efficacy and tolerability datapoints from an ongoing randomized Phase 2 trial in first-line RAS-mutated metastatic colorectal cancer.

Clinical and financial dependencies remain clear: the next update must provide more mature duration of response and PFS data to validate the early ORR advantage, and tolerability must remain favorable as follow-up accrues. The company reports $60.6 million in cash and investments as of September 30, 2025, with a projected runway into Q1 2027, and net cash used in operating activities of $10.8 million in 3Q25; both items define how long the program can advance without additional financing.

Watch the Q1 2026 trial update for confirmation of PFS and duration of response and track cash burn versus the stated runway into Q1 2027. Those two datapoints—mature efficacy tolerability readouts and remaining liquidity—are the immediate, monitorable items that will determine whether the early ORR signal translates into a materially positive clinical and corporate outcome.

– Announced positive data from the ongoing Phase 2 CRDF-004 trial evaluating onvansertib + standard of care for the treatment of first-line RAS-mutated metastatic colorectal cancer –

– Expects to report an update from the Phase 2 CRDF-004 trial in Q1 2026 –

– Cash and investments of $60.6 million as of September 30, 2025, projected runway into Q1 2027 –

SAN DIEGO, Nov. 06, 2025 (GLOBE NEWSWIRE) -- Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinical-stage biotechnology company leveraging PLK1 inhibition to develop novel therapies across a range of cancers, today announced financial results for the third quarter ended September 30, 2025, and provided a business update.

“This quarter was marked by highly encouraging data from our ongoing CRDF-004 trial evaluating onvansertib in combination with standard of care for first-line RAS-mutated mCRC. At the July 8, 2025 data cutoff, the 30mg onvansertib cohort demonstrated a 19% improvement in confirmed ORR, faster time to response, deeper tumor regression, and early signs of separation in the progression-free survival curves when compared to standard of care alone,” said Mark Erlander, Ph.D., Chief Executive Officer of Cardiff Oncology. “The study is on track for the next clinical update in the first quarter of 2026, where we’ll look for a continuation of onvansertib’s favorable tolerability profile and more mature duration of response and progression-free survival data.”

Continued Dr. Erlander, “Onvansertib is uniquely positioned to address a significant medical need and commercial opportunity, with approximately 150,000 new CRC patients diagnosed annually in the U.S. alone. With median progression-free survival of less than 12 months on standard of care and few promising therapies in development for RAS-mutated mCRC, we are optimistic that onvansertib has the potential to redefine first-line care for patients.”

Company highlights for the quarter ended September 30, 2025:

• Announced positive data from the ongoing CRDF-004 Phase 2 randomized trial evaluating two doses of onvansertib in combination with standard of care (“SoC”) for the treatment of first-line RAS-mutated metastatic colorectal cancer (“mCRC”)
  • As of the July 8, 2025 data cut-off, the Phase 2 CRDF-004 trial demonstrated a 19% improvement in confirmed objective response rate (“ORR”) in the 30mg onvansertib arm compared to the control arm in the intent-to-treat population.
  • While the median progression-free survival (“PFS”) has not yet been reached, early PFS data show a trend favoring the 30mg onvansertib arm versus control.
  • Dose dependent responses were observed across all endpoints, including ORR, PFS, early tumor shrinkage, and depth of response.
  • Onvansertib continues to be well-tolerated, with no major or unexpected toxicities observed.
    
• An update from the ongoing Phase 2 CRDF-004 trial in first-line RAS-mutated mCRC is expected in 1Q 2026.
  

Third Quarter 2025 Financial Results:

Liquidity, cash burn, and cash runway
As of September 30, 2025, Cardiff Oncology had approximately $60.6 million in cash, cash equivalents, and short-term investments.

Net cash used in operating activities for the third quarter of 2025 was approximately $10.8 million, an increase of $0.3 million from $10.5 million for the same period in 2024.

Based on its current expectations and projections, the Company believes its current cash resources are sufficient to fund its operations into Q1 2027.

Operating results
Total operating expenses were approximately $12.1 million for the three months ended September 30, 2025, a decrease of $0.7 million from $12.8 million for the same period in 2024. The decrease in operating expenses was primarily due to a reduction in clinical trial expenses and a decrease in preclinical activities.

About Cardiff Oncology, Inc.
Cardiff Oncology is a clinical-stage biotechnology company leveraging PLK1 inhibition, a well-validated oncology drug target, to develop novel therapies across a range of cancers. The Company's lead asset is onvansertib, a PLK1 inhibitor being evaluated in combination with standard of care (SoC) therapeutics in clinical programs targeting indications such as RAS-mutated metastatic colorectal cancer (mCRC), as well as in ongoing and planned investigator-initiated trials in metastatic pancreatic ductal adenocarcinoma (mPDAC), small cell lung cancer (SCLC) and metastatic triple negative breast cancer (mTNBC). These programs and the Company's broader development strategy are designed to target tumor vulnerabilities in order to overcome treatment resistance and deliver superior clinical benefit compared to the SoC alone. 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, 2024, 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.

Cardiff Oncology Contact:
James Levine
Chief Financial Officer
jlevine@cardiffoncology.com

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)
		Three Months Ended September 30,								Nine Months Ended September 30,
		2025				2024				2025				2024
Royalty revenues		$	120			$	165			$	350			$	532
Costs and expenses:
Research and development			8,197				9,640				30,254				27,140
Selling, general and administrative			3,897				3,126				11,229				9,471
Total operating expenses			12,094				12,766				41,483				36,611
Loss from operations			(11,974	)			(12,601	)			(41,133	)			(36,079	)
Other income (expense), net:
Interest income, net			716				741				2,492				2,472
Other income (expense), net			—				5				6				(37	)
Total other income (expense), net			716				746				2,498				2,435
Net loss			(11,258	)			(11,855	)			(38,635	)			(33,644	)
Preferred stock dividend			(6	)			(6	)			(18	)			(18	)
Net loss attributable to common stockholders		$	(11,264	)		$	(11,861	)		$	(38,653	)		$	(33,662	)
Net loss per common share — basic and diluted		$	(0.17	)		$	(0.25	)		$	(0.58	)		$	(0.74	)
Weighted-average shares outstanding — basic and diluted			66,879				46,865				66,644				45,461

Cardiff Oncology, Inc. Condensed Balance Sheets (in thousands) (unaudited)
		September 30, 2025				December 31, 2024
Assets
Current assets:
Cash and cash equivalents		$	10,135			$	51,470
Short-term investments			50,456				40,276
Accounts receivable and unbilled receivable			254				773
Prepaid expenses and other current assets			956				2,535
Total current assets			61,801				95,054
Property and equipment, net			666				898
Operating lease right-of-use assets			764				1,169
Other assets			549				69
Total Assets		$	63,780			$	97,190
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable		$	2,441			$	4,821
Accrued liabilities			11,539				7,897
Operating lease liabilities			726				710
Total current liabilities			14,706				13,428
Operating lease liabilities, net of current portion			284				813
Total Liabilities			14,990				14,241
Stockholders’ equity			48,790				82,949
Total liabilities and stockholders’ equity		$	63,780			$	97,190

FAQ

What did Cardiff Oncology (CRDF) report about the CRDF-004 trial on Nov 6, 2025?

Cardiff reported positive Phase 2 CRDF-004 data showing a 19% improvement in confirmed ORR for the 30mg onvansertib arm at the July 8, 2025 data cut-off and early PFS separation favoring 30mg.

When will Cardiff Oncology (CRDF) provide the next CRDF-004 clinical update?

The company expects to report an update from the Phase 2 CRDF-004 trial in Q1 2026.

How much cash did Cardiff Oncology (CRDF) have at Sept 30, 2025 and how long will it last?

Cardiff reported approximately $60.6 million in cash, cash equivalents, and short-term investments, projecting runway into Q1 2027.

What were Cardiff Oncology's (CRDF) Q3 2025 operating and cash-use metrics?

Total operating expenses were about $12.1M for Q3 2025 and net cash used in operating activities was approximately $10.8M.

What clinical benefits did the 30mg onvansertib cohort show in CRDF-004?

At the July 8, 2025 cut-off the 30mg cohort showed a 19% higher ORR, faster time to response, deeper tumor regression, and early signs of PFS separation versus control.

Does Cardiff say onvansertib is tolerable in the CRDF-004 trial (CRDF)?

Yes; the company reported that onvansertib continued to be well-tolerated with no major or unexpected toxicities observed.