CDSCO panel nod to Sun Pharma to study of anticancer drug Leuprolide acetate for depot suspension
The drug major Sun Pharma has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to conduct the bioequivalence study of anticancer drug Leuprolide acetate depot suspension 7.5mg/vial (1 Month Depot), a man-made form of gonadotropin-releasing hormone (GnRH) that is used in men to treat the symptoms of prostate...
The drug major Sun Pharma has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to conduct the bioequivalence study of anticancer drug Leuprolide acetate depot suspension 7.5mg/vial (1 Month Depot), a man-made form of gonadotropin-releasing hormone (GnRH) that is used in men to treat the symptoms of prostate cancer.
This came after the drug major Sun Pharma presented bioequivalence study protocol No. C1B03530, Version No. 01 dated 18-Sep-2023.
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Sun Pharma Gets CDSCO Panel Nod To Study Leuprolide Acetate For Depot Suspension
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