This page shows the latest Plasma therapy news and features for those working in and with pharma, biotech and healthcare.
Phase 3 results show the enzyme replacement therapy reduced thrombocytopenia events by 60%. ... The current standard of care (SoC) for cTTP is plasma therapy, which Takeda describes as ‘insufficient in restoring ADAMTS13, time-consuming, and costly’.
Takeda aims to develop an anti-SARS-CoV-2 polyclonal hyperimmune globin, a plasma-derived drug, which will harness the blood of coronavirus patients who have recovered from their infections. ... According to Takeda, plasma-derived therapies have
Takeda has started developing a plasma-derived therapy – a polyclonal hyperimmune globulin called TAK-888 – that is intended to treat high-risk individuals with the virus. ... The passive immunotherapy is produced from pathogen-specific antibodies
First in a new class of single-domain antibody fragments drugs. Sanofi has FDA approval for its acquired thrombotic thrombocytopenic purpura (aTTP) therapy Cablivi, the principle asset behind its 3.9bn ... The US approval – which comes a few months
deficiency. The product works as replacement therapy and temporarily increases plasma levels of factor X, helping to prevent and control bleeding, according to the EMA. ... new indications for Celgene's multiple myeloma therapy Revlimid (lenalidomide)
The new therapy is a plasma-derived Factor X that has been approved by the FDA for on-demand control, of bleeding episodes in patients aged over 12, as well as ... The US regulator notes that treatment is usually based on giving fresh plasma or
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