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After Blood Plasma Emergency Use Authorization, Can Takeda Develop A More Potent Alternative?

Hyperimmune Globulin Could Prove Superior

 
• By Andrew McConaghie

After the FDA's emergency use authorization for convalescent plasma, pushed on by President Trump, an alliance of firms is working with the NIH to conduct a robust study of a potentially more potent alternative.

Covid19_Plasma
Hyperimmune-globulin (H-Ig) is a more advanced version of convalescent plasma, which the alliance hope to demonstrate the benefits of in an NIH-sponsored trial.

A group of companies calling itself the “CoVIg-19 Plasma Alliance”, led by Takeda Pharmaceutical Company Limited. and CSL Behring, is poised to start a randomized trial for hyperimmune globulin – a potentially more potent and convenient alternative to convalescent plasma therapy.

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