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Reddy's gets DCGI nod for Zytorvi in cancer

By · Published by Everything Blog

In short

Dr. Reddy's has received DCGI approval for its drug Zytorvi, which is approved for the first-line treatment of adult patients with unresectable advanced, recurrent, or metastatic esophageal squamous cell carcinoma (ESCC) when combined with cisplatin and paclitaxel. This approval marks the second approved indication for Zytorvi in India, expanding beyond nasopharyngeal carcinoma.

Key points

  • Zytorvi receives DCGI approval for the second indication in India.: Zytorvi receives DCGI approval for the second indication in India.
  • The drug is approved for the treatment of esophageal squamous cell carcinoma.: The drug is approved for the treatment of esophageal squamous cell carcinoma.
  • The approval is supported by results from the Phase 3 JUPITER-06 trial, showing a 42% red…: The approval is supported by results from the Phase 3 JUPITER-06 trial, showing a 42% reduction in the risk of disease or death compared to chemotherapy alone.

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The drug has been approved in combination with cisplatin and paclitaxel for the first-line treatment of adult patients with unresectable advanced, recurrent, or metastatic ESCC, the pharma company said in a release.

Also Read: Biosimilars & innovation are Dr. Reddy’s growth pill: Generics to remain core business, says co-Chairman & MD GV Prasad

This marks Zytorvi's second approved indication in the country, expanding beyond nasopharyngeal carcinoma.

ESCC accounts for approximately 80 per cent of all esophageal cancer cases in India, the company said.

Zytorvi contains toripalimab, a monoclonal antibody that binds to PD-1 and blocks its interaction with PD-L1 and PD-L2, thereby supporting T-cell activity against cancer cells.

The approval is supported by results from the Phase 3 JUPITER-06 trial. In the study, toripalimab in combination with paclitaxel and cisplatin reduced the risk of disease or death by 42 per cent compared with chemotherapy alone, according to the release.

Also Read: Dr Reddy’s aims to resume semaglutide supply by November after API fix

At the final overall-survival analysis, median overall survival was 17.7 months with toripalimab plus chemotherapy compared with 12.9 months with chemotherapy alone, it added.

Dr. Reddy's holds commercialisation rights for toripalimab across 21 countries under a 2023 agreement with Junshi Biosciences.

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Original source: economictimes.indiatimes.com

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