Kura Oncology to present updated Phase 1a data at 2026 KCRS
Kura Oncology will present updated Phase 1a results from the FIT-001 trial evaluating darlifarnib plus cabozantinib in advanced RCC at the 2026 Kidney Cancer Research Summit. The data will highlight long-term follow-up in cabozantinib-naïve patients, supporting darlifarnib’s potential as a combination agent with VEGFR-targeted therapies. A global randomized Phase 1b study comparing the combination to cabozantinib alone is ongoing.

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Kura Oncology, Inc. will present updated Phase 1a results from the ongoing FIT-001 Phase 1a/1b clinical trial evaluating darlifarnib in combination with cabozantinib in advanced renal cell carcinoma (RCC) at the 2026 Kidney Cancer Research Summit (KCRS) in Boston. The presentation will feature long-term follow-up results in heavily pretreated cabozantinib-naïve patients with refractory RCC, providing further evidence of darlifarnib’s potential as a combination agent with VEGFR-targeted therapies. RCC is the most common form of kidney cancer, with clear cell RCC (ccRCC) accounting for more than 61,000 new cases in the U.S. annually.
The FIT-001 trial (NCT06026410) is a Phase 1a/1b study assessing the safety and efficacy of darlifarnib plus cabozantinib in advanced RCC. The updated Phase 1a data is expected to support darlifarnib’s potential to enhance VEGFR-targeted therapy in ccRCC. A global randomized Phase 1b study comparing darlifarnib plus cabozantinib versus cabozantinib alone is currently ongoing.
Key Trial Details
| Aspect | Details |
|---|---|
| Trial Name | FIT-001 Phase 1a/1b |
| ClinicalTrials.gov Identifier | NCT06026410 |
| Indication | Advanced Renal Cell Carcinoma (RCC) |
| Combination | Darlifarnib + Cabozantinib |
| Patient Population | Cabozantinib-naïve, advanced ccRCC |
The results continue to support darlifarnib as a precision combination agent across multiple targeted therapy classes. Kura Oncology has scheduled a virtual investor call on July 27, 2026, at 5:00 a.m. PT / 8:00 a.m. ET to discuss the updated data.
What are the anticipated timelines for the primary endpoint readouts from the ongoing global randomized Phase 1b study?
How might the long-term follow-up data influence the design of potential pivotal Phase 3 trials for this combination?
What specific biomarkers or patient subgroups will be analyzed to determine the precision potential of darlifarnib?




























