Johnson & Johnson statement on COVID 19 vaccine

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Melflufen filed with EMA for multiple myeloma – Oncopeptides AB

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Hypothesis for rare side effect linked to AstraZeneca vaccine

A hypothesis has been put forward as to why COVID-19 Vaccine AstraZeneca (ChAdOx1 nCov-19) seems to trigger an abnormal and potentially life-threatening combination of blood clotting and low platelet counts.Two research teams, each studying separate groups of patients came to similar conclusions. They both suggest the development of serious blood clots alongside falling levels of platelets — the sticky cells […]

FDA approves Trodelvy, the first treatment for metastatic triple-negative breast cancer shown to improve progression-free survival and overall survival – Gilead Sciences

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FibroGen provides additional information on roxadustat to the FDA relating to U.S. primary cardiovascular safety analyses

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Complete Response Letter for sBLA for Keytruda in high-risk early-stage triple-negative breast cancer (TNBC) – Merck Inc.

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Evrysdi approved by European Commission as first and only at home treatment for spinal muscular atrophy – Roche

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EU approves SC version of Tysabri for multiple sclerosis – Biogen

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FDA approval of additional indication for Vyxeos for the treatment of secondary acute myeloid leukemia in pediatric patients – Jazz Pharma

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New real-world observational analysis of Uptravi underscores the importance of risk assessment for treating pulmonary arterial hypertension patients -Johnson & Johnson

Findings from an analysis of the first 500 patients enrolled in the SPHERE registry (SelexiPag: tHe usErs dRug rEgistry) found more than three-quarters (76%) of pulmonary arterial hypertension (PAH) patients treated with Uptravi (selexipag)from Johnson & Johnson, either maintained (56%) or reduced (20%) their one-year mortality risk score. The SPHERE results were published in the April issue of the Journal […]