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Lisata Therapeutics’ Certepetide Granted FDA Orphan Drug Designation for the Treatment of Cholangiocarcinoma

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Lisata Therapeutics

Lisata Therapeutics’ Certepetide Granted FDA Orphan Drug Designation for the Treatment of Cholangiocarcinoma

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  • The US FDA has granted orphan drug designation to the company’s certepetide for treating cholangiocarcinoma
  • Certepetide is being assessed under the P-IIa clinical evaluation for its preliminary efficacy, safety and tolerability in addition to SoC vs PBO + SoC alone as a 1L and 2L treatment of cholangiocarcinoma
  • Certepetide activates the C-end rule transport mechanism for effective tumor-specific delivery of co-administered anti-cancer drugs. It also reduces immunosuppression and inhibit metastasis by modifying the tumor microenvironment

Ref: Lisata Therapeutics | Image: Lisata Therapeutics

Related News:- Taiho Oncology Europe GmbH and Taiho Pharmaceutical Receive EC’s Conditional Marketing Authorization for Lytgobi to Treat Cholangiocarcinoma

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Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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