- CEL-SCI Corporation CVM said that its 10-year Phase 3 trial showed that Multikine immunotherapy significantly extended the lives of patients with locally advanced primary squamous cell carcinoma of the head and neck (SCCHN).
- The company says that current drug therapies for SCCHN from Merck & Co Inc MRK and Bristol Myers Squibb & Co BMS are approved as a last resort.
- The Multikine treated study population showed the following advantages over control:
- A median overall survival improvement of 46.5 months—nearly four years.
- 62.7% of Multikine patients were alive after five years vs. 48.6% in control.
- Nearly one out of every six patients had their tumors shrink by more than 30% in three weeks.
- Five patients had their tumors completely disappear in just three weeks.
- Tumor shrinkage/disappearance cut the death rate by a factor of three.
- Merck's drug Keytruda was approved for recurrent SCCHN based on a single-arm trial with a 16% tumor response rate. CVM says a randomized controlled trial showed the same response rate.
- Keytruda did not show a survival improvement versus a 29% survival improvement for CVM's immunotherapy.
- BMS's drug Opdivo was approved based on only a 2.4-month life extension. The company's immunotherapy showed a median 46-month improvement in life extension.
- Furthermore, CVM highlights Multikine's favorable toxicity profile than these approved products.
- Price Action: CVM shares are up 3.19% at $2.91 on the last check Tuesday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
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