RedHill Biopharma to Submit FDA-Approved Talicia® for UK Marketing Authorisation
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RedHill Biopharma plans to submit Talicia for UK marketing authorization using the MHRA's fast-track process, referencing its FDA approval. Potential UK approval is expected in Q4 2025.
March 18, 2025 | 11:30 am
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RedHill Biopharma is preparing to submit Talicia for UK marketing authorization, leveraging the MHRA's fast-track process. This could lead to UK approval by Q4 2025, expanding Talicia's market reach.
The submission of Talicia for UK marketing authorization is a significant step for RedHill Biopharma, as it could expand the drug's market reach. The use of the MHRA's fast-track process, referencing FDA approval, suggests a streamlined path to approval, which is positive for the company's growth prospects.
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