Pfizer Gets CDSCO Panel Nod To study anti-cancer drug Lorlatinib Dr. Divya Colin24 March 2024 5:45 PM ISTNew Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Zydus Lifesciences receives tentative approval from USFDA for Letermovir Tablets Ruchika Sharma24 March 2024 2:30 PM ISTLetermovir tablets are used to prevent disease caused by a virus called cytomegalovirus in people who have received a bone marrow transplant or kidney...
Novartis Fabhalta gets positive CHMP opinion as first oral monotherapy for adult patients with paroxysmal nocturnal hemoglobinuria Ruchika Sharma24 March 2024 2:30 PM ISTBasel: Novartis has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a...
Gilead Sciences completes acquisition of CymaBay Therapeutics for USD 4.3 billion Ruchika Sharma24 March 2024 11:00 AM ISTAs a result of the completion of the merger, CymaBay has become a wholly owned subsidiary of Gilead.
Bill & Melinda Gates Medical Research Institute begins Phase 3 clinical trial of Tuberculosis vaccine Ruchika Sharma24 March 2024 10:00 AM ISTCambridge: The Bill & Melinda Gates Medical Research Institute (Gates MRI) has announced that a Phase 3 clinical trial to assess the efficacy of...
Novo Nordisk Awiqli recommended for approval for diabetes by European regulatory authorities Ruchika Sharma23 March 2024 2:12 PM ISTAwiqli is a once-weekly basal insulin analogue designed to cover the basal insulin requirements for a full week with a single subcutaneous injection.
USFDA grants full approval for Abbvie Elahere for certain ovarian cancer patients Ruchika Sharma23 March 2024 1:15 PM ISTNorth Chicago, Ill.: AbbVie has announced that the U.S. Food and Drug Administration (FDA) has granted full approval for ELAHERE...
Merck Speciality gets CDSCO Panel Nod To study anti-cancer drug Avelumab Dr. Divya Colin22 March 2024 5:45 PM ISTNew Delhi: The drug major Merck Speciality has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
USFDA successfully concludes inspection at Neuland Labs Bonthapally facility Ruchika Sharma22 March 2024 4:31 PM ISTHyderabad: Neuland Laboratories Limited has announced that the United States Food and Drug Administration (US FDA) has successfully...
Bristol Myers Squibb Abecma approved in European Union for triple-class exposed relapsed and refractory multiple myeloma Ruchika Sharma22 March 2024 4:02 PM ISTPrinceton: Bristol Myers Squibb has announced that the European Commission (EC) has granted approval to Abecma (idecabtagene vicleucel;...
Takeda bags accelerated USFDA nod for Iclusig with chemotherapy in adult patients with newly diagnosed Ph+ ALL Ruchika Sharma22 March 2024 11:57 AM ISTOsaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Application (sNDA) for...
CDSCO Panel grants GSK's Updated Prescribing Information for Antibiotic FDC of Amoxicillin, Clavulanic acid Dr. Divya Colin21 March 2024 5:45 PM ISTNew Delhi: The drug major GSK has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation...
