Biotech & Genomic Medicine▲
Inhibrx Cancer Drug Nearly Doubles Keytruda Response Rate, Stock Falls 8.8%
Inhibrx Biosciences said its experimental cancer drug INBRX-106 combined with Merck's Keytruda produced a confirmed objective response rate of 48.3% versus 26.5% for Keytruda alone in the Phase 2 portion of its HexAgon study in treatment-naive, PD-L1-positive metastatic or unresectable recurrent head and neck squamous cell carcinoma. The study enrolled 68 patients, with 63 evaluable for the primary endpoint, and four patients, or 13.8%, on the combination achieved a complete response versus none on Keytruda alone. Median progression-free survival was 9.6 months for the combination versus 4.9 months for Keytruda alone as of the August 19 data cutoff, and among 10 evaluable HPV-positive patients the confirmed response rate was 80% versus 33.3% among nine patients on Keytruda alone. Inhibrx plans to add approximately 50 HPV-positive oropharyngeal cancer patients to the Phase 2 study to support a potential accelerated regulatory pathway, estimating the U.S. could have approximately 30,000 HPV-positive head and neck cancer patients by 2029, including around 6,000 first-line recurrent patients, representing a $1 billion annual sales opportunity. Despite the data, Inhibrx shares fell 8.8% to $110.45, a move CEO Mark Lappe told Reuters the company could not explain, while Stifel analyst Dara Azar called the results competitive against the difficult OX40 target.
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Biotech & Genomic Medicine › Immuno-Oncology / Checkpoint ▲Technology
Biotech & Genomic Medicine › Oncology Therapeutics ▲Technology
INBX · Technology · Positive INBRX-106 plus Keytruda nearly doubled confirmed response rate (48.3% vs 26.5%) and improved PFS in the HexAgon Phase 2 study.
MRK · Technology · Positive Keytruda was the backbone comparator and the combination showed markedly better response rates than Keytruda alone.