Eli Lilly Gets CDSCO Panel Nod To Import, Market Lasmiditan for acute treatment of migraine
New Delhi: Citing that the global clinical trial data demonstrate the efficacy and safety of Lasmiditan for the acute treatment of migraine with and without aura, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has granted approval to drug major Eli Lilly to import and market Lasmiditan 50 mg and 100 mg tablets.
This approval is subject to the condition that the firm conduct a Phase IV clinical trial of the product in the country, for which a protocol should be submitted to CDSCO within two months of the drug's approval.
This came after the drug major Eli Lilly presented its proposal to import and market Lasmiditan 50 mg and 100 mg tablets, along with a global Phase III clinical trial report, before the committee.
Lasmiditan is an oral 5HT1F agonist used for the acute treatment of migraine headache with or without aura. Lasmiditan was first approved for use in the United States in October 2019. It was also approved by the European Commission on August 17, 2022.
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