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Delcath Systems’ Hepzato KIT Receives the US FDA’s Approval for Adult Patients with Unresectable Hepatic-Dominant Metastatic Uveal Melanoma

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Delcath Systems

Delcath Systems’ Hepzato KIT Receives the US FDA’s Approval for Adult Patients with Unresectable Hepatic-Dominant Metastatic Uveal Melanoma

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  • The US FDA has approved Hepzato KIT (melphalan/Hepatic Delivery System) as a liver-directed treatment for adult patients with mUM with unresectable hepatic metastases. The approval was based on the results from the P-III study (FOCUS) of Hepzato KIT via the hepatic delivery system (HDS) during a PHP procedure in 91 patients
  • The results showed ORR was 36.3% in patients with hepatic and extrahepatic lesions and m-DoR was 14mos., DCR was 73.6% with 7 complete responses (7.7%), and PR (28.6%)
  • The product is expected to be available in Q4’23 and enrolled patients will continue treated at Expanded Access Program (EAP) sites. Hepzato Kit is supplied with the Hepzato 5×5 Drug Pack and the HDS

Ref: PR Newswire | Image: Delcath Systems

Related News:- Foghorn Therapeutics Reports Discontinuation of P-I Clinical Trial for FHD-286 in Metastatic Uveal Melanoma (mUM)

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Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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