EX-99.1 2 crdf033123-q12023pr.htm EX-99.1 Document

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Cardiff Oncology Reports First-Quarter 2023 Results and Provides Business Update

First Patient Dosed in ONSEMBLE Phase 2 Randomized Trial of Onvansertib in Patients with KRAS/NRAS-mutated Metastatic Colorectal Cancer (mCRC)

Introduced full membership of Scientific Advisory Board (SAB)

Announced appointment of Fairooz Kabbinavar, MD, FACP, as Chief Medical Officer

Cash, cash equivalents, and short-term investments of approximately $97 million as of March 31, 2023, projected runway into 2025

SAN DIEGO, May 4, 2023 - Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinical-stage biotechnology company leveraging PLK1 inhibition, a well-validated oncology drug target, to develop novel therapies across a range of cancers, today announced financial results for the first-quarter ended March 31, 2023, and provided a business update.

“We are delighted to have dosed the first patient in our Phase 2 ONSEMBLE trial. This randomized trial will evaluate the efficacy of onvansertib combined with standard of care in patients with KRAS/NRAS-mutated mCRC, who historically have limited treatment options,” said Mark Erlander, PhD, Chief Executive Officer of Cardiff Oncology. “In addition, we are excited to have appointed Fairooz Kabbinavar, MD, FACP, as our new Chief Medical Officer, who brings deep expertise in the treatment of patients with CRC as well as expertise in using bevacizumab in the clinical setting. We believe Dr. Kabbinavar adds significant value to our clinical development program for onvansertib. We also formally introduced the full membership of our Scientific Advisory Board, a group of highly esteemed oncology experts who are providing a diverse range of insights that strengthen our clinical programs.”

Upcoming potential milestones

•Metastatic pancreatic ductal adenocarcinoma (mPDAC) data readout from Phase 2 trial expected in mid-2023
•Small cell lung cancer (SCLC) data readout from investigator-initiated (with UPMC) Phase 2 trial expected in mid-2023
•Triple negative breast cancer (TNBC) data readout from investigator-initiated (with Dana-Farber Cancer Institute) Phase 1b/2 trial expected in the fourth-quarter of 2023 or first-quarter of 2024
•mCRC randomized data readout from Phase 2 ONSEMBLE trial expected in the second-half of 2024

Company Highlights for the quarter ended March 31, 2023

•Announced the Appointment of Fairooz Kabbinavar, MD, FACP, as Chief Medical Officer. Dr. Kabbinavar oversees the clinical development program for the Company's investigational drug onvansertib and reports directly to Chief Executive Officer, Mark Erlander, PhD.
•Formally introduced the full membership of its Scientific Advisory Board (SAB). The SAB is comprised of a distinguished group of academic and industry experts who bring depth and breadth of knowledge in oncology drug development, clinical trial design, translational science and clinical research. In most cases, these individuals have been advising the Company for several years and will now collectively serve a critical role as we advance the clinical development of


onvansertib. The Company anticipates that over time the membership of the SAB may expand to add additional expertise in new indications or stages of clinical development.
•Announced First Patient Dosed in ONSEMBLE Phase 2 Randomized Trial of Onvansertib in Patients with Metastatic Colorectal Cancer. The Phase 2 ONSEMBLE trial includes patients with mCRC who have a documented KRAS or NRAS mutation and have previously received one prior chemotherapy regimen with or without bevacizumab in the first line metastatic setting. Patients are being randomized to onvansertib plus FOLFIRI/bevacizumab versus FOLFIRI/bevacizumab (standard of care).

First-Quarter 2023 Financial Results

Liquidity, cash burn, and cash runway

As of March 31, 2023, Cardiff Oncology had approximately $97.0 million in cash, cash equivalents, and short-term investments.

Net cash used in operating activities for the first quarter of 2023 was approximately $8.7 million, a decrease of approximately $1.5 million from $10.2 million for the same period in 2022.

Based on its current expectations and projections, the Company believes its current cash resources are sufficient to fund its operations into 2025.

Operating results

Total operating expenses were approximately $12.1 million for the three months ended March 31 2023, an increase of $1.0 million from $11.1 million for the same period in 2022. The increase in operating expenses was primarily due to higher costs associated with clinical programs and outside service costs related to the development of the company’s lead drug candidate, salaries and staff costs primarily due to increased headcount.

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 KRAS/NRAS-mutated metastatic colorectal cancer (mCRC) and metastatic pancreatic ductal adenocarcinoma (mPDAC), as well as in investigator-initiated trials in triple negative breast cancer (TNBC) and small cell lung cancer (SCLC). 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; risks related to business interruptions, including the outbreak of COVID-19 coronavirus, 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 any precision medicine therapeutics 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, 2022, 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 
858-952-7670 
jlevine@cardiffoncology.com 

Investor Contact:  
Kiki Patel, PharmD  
Gilmartin Group  
332-895-3225
Kiki@gilmartinir.com 

Media Contact:  
Richa Kumari 
Taft Communications  
551 344-5592   
richa@taftcommunications.com 
SOURCE Cardiff Oncology, Inc.




Cardiff Oncology, Inc.
Condensed Statements of Operations
(in thousands, except for per share amounts)
(unaudited)
Three Months Ended March 31,
20232022
Royalty revenues$83 $74 
Costs and expenses:
Research and development9,052 7,208 
Selling, general and administrative3,083 3,940 
Total operating expenses12,135 11,148 
Loss from operations(12,052)(11,074)
Interest income, net940 130 
Other income (expense), net(111)(49)
Net loss (11,223)(10,993)
Preferred stock dividend(6)(6)
Net loss attributable to common stockholders$(11,229)$(10,999)
Net loss per common share — basic and diluted$(0.25)$(0.25)
Weighted-average shares outstanding — basic and diluted44,677 43,231 



Cardiff Oncology, Inc.
Condensed Balance Sheets
(in thousands)
(unaudited)
March 31, 2023December 31, 2022
Assets
Current assets:
Cash and cash equivalents$15,017 $16,347 
Short-term investments81,951 88,920 
Accounts receivable and unbilled receivable676 771 
Prepaid expenses and other current assets4,109 5,246 
Total current assets101,753 111,284 
Property and equipment, net1,320 1,269 
Operating lease right-of-use assets2,115 2,251 
Other assets1,361 1,387 
Total Assets$106,549 $116,191 
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable$2,914 $1,956 
Accrued liabilities4,555 5,177 
Operating lease liabilities679 675 
Total current liabilities8,148 7,808 
Operating lease liabilities, net of current portion1,898 2,040 
Total Liabilities10,046 9,848 
Stockholders’ equity96,503 106,343 
Total liabilities and stockholders’ equity$106,549 $116,191 




Cardiff Oncology, Inc.
Condensed Statements of Cash Flows
(in thousands)
(unaudited)
Three Months Ended March 31,
20232022
Operating activities
Net loss$(11,223)$(10,993)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation90 31 
Stock-based compensation expense1,064 1,152 
Amortization of premiums on short-term investments(163)346 
Release of clinical trial funding commitment— 139 
Changes in operating assets and liabilities1,573 (924)
Net cash used in operating activities(8,659)(10,249)
Investing activities:
Capital expenditures(8)(171)
Net purchases, maturities and sales of short-term investments7,337 18,529 
Net cash provided by investing activities7,329 18,358 
Financing activities:
Net cash provided by financing activities— — 
Net change in cash and cash equivalents(1,330)8,109 
Cash and cash equivalents—Beginning of period16,347 11,943 
Cash and cash equivalents—End of period$15,017 $20,052