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Glenmark receives acceptance from U.S. FDA for Phase 1/2, first-in-human clinical study of GRC 54276
Glenmark Specialty SA, has received acceptance from the U.S. FDA on its IND application for GRC 54276 to proceed with a Phase 1/2, first-in-human, clinical study of GRC 54276 for the treatment of patients with advanced solid tumors and lymphomas.
India
Drug-administration
Glenmark-pharmaceuticals
Medicine-group
Glenmark-pharmaceuticals-ltd
Investigational-new-drug
Nikhil-amin
Glenmark-pharmaceuticals-limited
Glenmarkpharmaceuticals
Ine935a01035
Glenmarkspecialtysa
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