
Cardiff Oncology CEO Faces FDA Trial Endpoint Risk as Q1 Data Nears
Cardiff Oncology's pivotal trial for RAS-mutated metastatic colorectal cancer may fail to meet FDA endpoints when data drops in Q1 2026. CEO Mark Erlander oversees a development program facing potential regulatory rejection that could eliminate the market approval pathway. The medium-likelihood, catastrophic-severity risk arrives as oncology biotechs face heightened FDA scrutiny.


