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Zydus Cadila Saroglitazar secures USFDA Fast Track Designation to treat Primary Biliary Cholangitis

Ruchika SharmaWritten by Ruchika Sharma Published On 2020-12-10T12:27:35+05:30  |  Updated On 10 Dec 2020 12:27 PM IST
Zydus Cadila Saroglitazar secures USFDA Fast Track Designation to treat Primary Biliary Cholangitis
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Ahmedabad: Drugmaker, Zydus Cadila, has recently announced that United States Food and Drug Administration (USFDA) has granted "Fast Track Designation" to Saroglitazar Mg for the treatment of patients with Primary Biliary Cholangitis (PBC).

Fast Track is a process of the USFDA which expedites the review of drugs to treat serious conditions and fill an unmet medical need. A drug that receives Fast Track designation is eligible for Accelerated Approval and Priority Review, if the relevant criteria are met. The purpose is to get important new drugs to the patients faster.

The global market for primary biliary cholangitis treatment is expected to grow at a CAGR of 36.3% from 2018 – 2026 and is expected to reach USD 10.8 bn by 2026 as per Coherent market insights.

Saroglitazar Mg is a potent and selective peroxisome proliferator-activated receptor alpha and gamma dual agonist. Results of PHASE 2, prospective multicentre randomized double-blind, placebocontrolled study to evaluate the safety, tolerability and efficacy of Saroglitazar Mg in patients with PRIMARY BILIARY CHOLANGITIS (EPICS) was presented earlier at the The Liver Meeting 2020, the Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) [ClinicalTrials.gov Identifier: NCT03112681]. The treatment options are still evolving for primary biliary cholangitis and Saroglitazar holds immense potential based on its safety and efficacy profile so far.

Speaking on the development, Pankaj R. Patel, Chairman, Zydus Cadila said, "The awarding of Fast Track Designation to Saroglitazar, an investigational candidate for the treatment of PBC, is an important recognition by USFDA to address the serious condition and bridge an unmet medical need in the treatment of PBC patients. We are very thankful to the USFDA for their timely and useful feedback on the clinical trial designs of Saroglitazar Mg and will continue to work closely with the USFDA for Clinical Development for Saroglitazar Mg for patients with Primary Biliary Cholangitis (PBC)."

Read also: Zydus Cadila gets DCGI nod for Phase 1 trial of novel molecule ZYIL1




zydus cadilazydus cadila newsusfdasaroglitazarprimary biliary cholangitis
Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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