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COVID-19 pandemic: IAS 2021 urges rich states to ensure availability of vaccines to poor countries

July 19, 2021 LAHORE: Whereas COVID-19 pandemic exacerbated many inequalities worldwide, the IAS 2021 has put moral obligation upon rich countries to ensure in real time availability of vaccines to low and middle-income countries coping with the challenges of accessibility. “If the world is dealing with a pandemic involving everyone and anyone, the common enemy is the virus, and not the people one’s having disagreement with. The global pandemic requires a global response, and therefore calls upon the entire world to pull together in a synergistic way to address a global pandemic,” says Dr Anthony Fauci, Director National Institute of Allergy and Infectious Diseases (NIAID) at the US National Institutes of Health, while speaking Sunday at a panel discussion titled “From pandemic to pandemic” at opening session of IAS 2021- the 11th IAS Conference on HIV Science - virtually convened by International AIDS Society. Dr Eckart

Xenikos Announces T-Guard® Phase 3 Clinical Update and Outlines 2021-2022 Corporate Objectives

Share: Company Plans to Commence New Pivotal, Randomized Phase 3 Study Evaluating T-Guard ® Versus Ruxolitinib in Patients with Grade III or IV Steroid-refractory Acute Graft-Versus-Host Disease in Second Half of 2021 Positive Results Expected to Support Both FDA and EMA Regulatory Submissions NIJMEGEN, the Netherlands, July 19, 2021 (GLOBE NEWSWIRE) Xenikos B.V., a privately-held biotechnology company that develops innovative immunotherapies for treating patients with severe immune disease and post-transplant rejection, today announced that it has reached agreement with the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) on the design of its pivotal randomized Phase 3 clinical study (BMT CTN 2002) to evaluate T-Guard

Xenikos B V : Xenikos Announces T-Guard Phase 3 Clinical Update and Outlines 2021-2022 Corporate Objectives

Xenikos B.V.: Xenikos Announces T-Guard Phase 3 Clinical Update and Outlines 2021-2022 Corporate Objectives Company Plans to Commence New Pivotal, Randomized Phase 3 Study Evaluating T-Guard Versus Ruxolitinib in Patients with Grade III or IV Steroid-refractory Acute Graft-Versus-Host Disease in Second Half of 2021 Positive Results Expected to Support Both FDA and EMA Regulatory Submissions NIJMEGEN, the Netherlands, July 19, 2021 (GLOBE NEWSWIRE) Xenikos B.V., a privately-held biotechnology company that develops innovative immunotherapies for treating patients with severe immune disease and post-transplant rejection, today announced that it has reached agreement with the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) on the design of its pivotal randomized Phase 3 clinical study (BMT CTN 2002) to evaluate T-Guard

NRx Pharmaceuticals Presents Evidence ZYESAMI™ (aviptadil) Helps Prevent Cytokine Storm in Patients with COVID-19

NRx Pharmaceuticals Presents Evidence ZYESAMI™ (aviptadil) Helps Prevent Cytokine Storm in Patients with COVID-19
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