Cardiff Oncology, Inc. (CRDF) is a clinical-stage biotechnology company committed to developing treatments for cancers with the greatest unmet medical need. Formerly known as Trovagene, Inc., this San Diego-based firm primarily focuses on addressing tumors that have significant driver mutations, present resistance to existing therapies, or affect underdiagnosed segments.
One of Cardiff Oncology's key assets is Onvansertib, a unique cancer treatment platform. This is a first-in-class, third-generation, oral and highly-selective Polo-like Kinase 1 (PLK1) Inhibitor. PLK1 is an enzyme that is-overexpressed in multiple types of cancer, and its inhibition has demonstrated to halt cell division and lead to cancer cell death. The firm is currently pursuing clinical trials focusing on colorectal, prostate, and leukemia cancers.
In prostate cancer, Cardiff Oncology has adopted the combination strategy with Onvansertib and Zytiga, an androgen receptor signaling inhibitor. For colorectal cancer, they are combining Onvansertib with Folfiri and Avastin, chemotherapy and vascular endothelial growth factor inhibitor drugs respectively. In acute myeloid leukemia, they are using Onvansertib in combination with decitabine, a hypomethylating agent.
These synergistic approaches aim to improve efficacy and circumvent resistance that often develops with single-agent therapies in cancer treatment. The combination also allows lower doses, which could result in lesser side effects. Furthermore, Onvansertib could be paired with other cancer therapies, thus providing Cardiff Oncology with many potential pathways for commercialization.
Cardiff Oncology has a strategic license agreement with Nerviano Medical Sciences, which grants them exclusive worldwide rights to research, develop, manufacture, and commercialize Onvansertib. The company's dedication about creating innovative therapies for patients who currently lack options keeps their research activities robust.
Cardiff Oncology operates in a fast-paced industry, and the regulatory environment of drug development is both complex and challenging. However, the firm's ambitious approaches and use of next-generation technology position it as an exciting, pivotal player in the fight against cancer.
Its leadership comprises a team of highly-experienced industry leaders who have successfully developed and commercialized various novel therapies. Thus, investors hope that Cardiff Oncology's bold strategies would pave the way to successful therapies, providing returns while making significant contributions to the health sector.
Their progress and success serve both a promise of hope for those engaged in the battle against cancer and a prime example of progressive, patient-centric biotechnology to their industry counterparts. Cardiff Oncology symbolizes the intersection of innovation, technology, and commitment to change cancer care for the better.
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Cardiff Oncology and Nerviano Medical Sciences have amended their 2017 Exclusive License Agreement, resolving disputes over global rights for onvansertib and establishing a collaborative framework for its clinical development. This amendment clarifies the royalty structure, includes development objectives for Cardiff's Phase 3 program, and grants NMS the right to appoint a Board observer and join Cardiff's Scientific Advisory Board. Both companies expressed commitment to advancing onvansertib, a PLK1 inhibitor, for patients with RAS-mutated metastatic colorectal cancer.

Cardiff Oncology, Inc. announced its participation in two upcoming conferences in September 2026. Mani Mohindru, Ph.D. will discuss advancing PLK1 targeted therapy for RAS mutant metastatic colorectal cancer at the 8th Annual RAS-Targeted Drug Development Summit and participate in a fireside chat at the H.C. Wainwright 28th Annual Global Investment Conference. Details and webcasts for these events will be available on the company's website.
Zacks Research increased its Q3 2026 EPS estimate for Cardiff Oncology (NASDAQ:CRDF) to a loss of $0.15 per share, with full-year 2026 estimates now at a loss of $0.64 per share. Despite the slight improvement in the Q3 estimate, analyst sentiment has generally weakened, leading to an average "Hold" rating and a $7.50 price target. The company recently reported a Q2 loss of $0.14 per share, missing expectations, and company insiders have recently purchased shares.