Eris Lifescience gets CDSCO panel nod to study FDC of Metoprolol Succinate, Dapagliflozin
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New Delhi: Directing to present bioequivalence (BE) study results in the Subject Expert Committee (SEC) before initiating the Phase III clinical trial, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organization (CDSCO) has granted approval to drug maker Eris for conducting bioequivalence (BE) study and Phase III clinical trial of the fixed-dose combination drug Metoprolol Succinate plus Dapagliflozin.
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