Bristol Myers Squibb`s Biologic Orencia (abatacept) Receives Approval in the U.S.
Coya Therapeutics, Inc. Announces an Agreement with Dr. Reddy’s Laboratories, Ltd. to License its proposed biosimilar Abatacept for the Development and Commercialization of COYA 302 for the Treatment of Neurodegenerative Diseases
UNC Gillings School of Global Public Health has reported topline results from the US National Institutes of Health (NIH)-led clinical trial where immune modulator drugs, infliximab or abatacept, showed to boost survival in hospitalised Covid-19 adult patients.
Bristol Myers Squibb (BMS) has reported topline data from the Phase III ACTIV-1 Immune Modulators clinical trial, where treatment with Orencia (abatacept) boosted survival in individuals admitted to the hospital with Covid-19.
A large randomised, placebo-controlled clinical trial led by the National Institutes of Health (NIH) has shown that treating adults hospitalised with COVID-19 with infliximab or abatacept – drugs widely used to treat certain autoimmune diseases – did not significantly shorten time to recovery, but substantially improved clinical status and reduced deaths.
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Now comes another boost from the FDA with a nod as a preventative therapy for transplant rejection. On Wednesday, the U.S. drug regulator endorsed Orencia for the prevention of acute graft-versus-host disease (GVHD) in combination with certain immunosuppressants.
BMS` Orencia snagged priority review in transplant rejection
Bristol Myers`s Orencia (Abatacept ) Receives Supplemental Approval in US
With megablockbuster Humira on the decline, AbbVie is hoping for big things from its next-gen JAK inhibitor Rinvoq. Now, in a head-to-head rheumatoid arthritis battle with Bristol Myers Squibb's blockbuster Orencia, Rinvoq has come out on top.