Fulgent Genetics said updated phase 2 data for fid-007 in combination with cetuximab showed an objective response rate of 61.9% in patients with recurrent or metastatic head and neck squamous cell carcinoma whose disease had progressed after PD-1–based therapy.
The company said median progression-free survival was 6.7 months, median duration of response was 7.4 months, and one-year overall survival was 63.4% as of the April 16, 2026 data cutoff.
The study is testing two dosing regimens in an open-label, randomized phase 2 trial. Fulgent said the combination showed activity in both HPV-related and HPV-unrelated disease, and that the safety profile was manageable.
The company said a phase 3 study is planned. Following these announcements, the company's shares moved 0.66%, and are now trading at a price of $18.26. For the full picture, make sure to review Fulgent Genetics's 8-K report.
