WebProdutos, BMS, Bristol-Myers Squibb Pharma EEIG - INDICE.eu - Toda a Saúde Web3024701 4 0.4 10. 2349502 1 300 1.333. 2500901 1 1E-3 3.5. 2502201 1 5.0000000000000001E-3 7. 2502202 1 5.0000000000000001E-3 1. 2690701 1 1 0.5. 2723401 1 0.1 0.5. 2770201 1 5.00
Bristol-Myers Squibb Receives Accelerated Approval of Opdivo (nivolumab ...
WebList of results by case. List of documents. Search result: 1 case (s) 1 documents analysed. 1/1. T-329/16 - Bristol-Myers Squibb Pharma v Commission and EMA. [Case closed] Main proceedings. Judgment of the General Court (Second Chamber) of 5 December 2024. Bristol-Myers Squibb Pharma EEIG v European Commission and European Medicines … WebBristol-Myers Squibb/Astrazeneca EEIG . Bristol-Myers Squibb/Pfizer EEIG Bristol-Myers Squibb/Sanofi Pharmaceuticals Partnership . Britcair Limited . Compania Bristol-Myers Squibb de Centro America . Convatec-Produtos Medicos, Limitada . E. R. Squibb & Sons Inter-American Corporation . E. R. Squibb & Sons Limited . E. R. Squibb & Sons, … cummins power club
Bristol-Myers Squibb Pharma EEIG - European Medicines Agency
WebOPDIVO 120615/1 187053/13 PERJETA 420MG 420mg/14ml Roche Diagnostics GmbH 182416/1 TECENTRIQ 181919/1 F. Hoffmann La Roche Ltd, Kaiseraugst 38420/1 840mg/18ml F. Hoffmann La Roche Ltd, Basel Manufacturing site Kaiseraugst 80114/1 YERVOY Takeda Pharma AS Bristol-Myers Squibb Company E2 179019/1 … Web1 On 17 May 2012, the applicant, Bristol-Myers Squibb Pharma EEIG, submitted to the European Medicines Agency (EMA) an application for the designation of Elotuzumab as an orphan medicinal product indicated for the treatment of … Web23 de jan. de 2016 · Bristol-Myers Squibb Company (NYSE:BMY) today announced that the U.S. Food and Drug Administration (FDA) has approved Opdivo (nivolumab) in combination with Yervoy (ipilimumab) for the treatment of patients with BRAF V600 wild-type and BRAF V600 mutation-positive unresectable or metastatic melanoma. 1 This … easy acoustic cdlc