Pemivibart

Source: Wikipedia, the free encyclopedia.

Pemivibart
SARS-CoV-2
Clinical data
Trade namesPemgarda
Other namesVYD222
License data
Intravenous
ATC code
  • None
Legal status
Legal status
Identifiers
CAS Number
UNII
KEGG

Pemivibart, sold under the brand name Pemgarda, is a monoclonal antibody medication authorized for the pre-exposure prophylaxis (prevention) of COVID‑19.[3]

The US

emergency use authorization for pemivibart in March 2024.[3][4]

Medical uses

In the US, pemivibart is authorized for the pre-exposure prophylaxis (prevention) of COVID‑19 in certain adults and adolescents (12 years of age and older weighing at least 40 kilograms (88 lb).[3] It is authorized for individuals who are not currently infected with SARS‑CoV‑2 and who have not had a known recent exposure to an individual infected with SARS‑CoV‑2; and who have moderate-to-severe immune compromise due to a medical condition or due to taking immunosuppressive medications or treatments and are unlikely to mount an adequate immune response to COVID‑19 vaccination.[3]

Society and culture

Names

Pemivibart is the international nonproprietary name.[5]

References

  1. ^ "Emergency Use Authorization: PEMGARDA (pemivibart)". U.S. Food and Drug Administration. 22 March 2024.
  2. ^ "Highlight of Emergency Use Authorization: PEMGARDA (pemivibart)". U.S. Food and Drug Administration. Archived from the original on 23 March 2024. Retrieved 23 March 2024.
  3. ^ a b c d "FDA Roundup: March 22, 2024". U.S. Food and Drug Administration (FDA). 22 March 2024. Archived from the original on 23 March 2024. Retrieved 23 March 2024. Public Domain This article incorporates text from this source, which is in the public domain.
  4. ^ "Invivyd Announces FDA Authorization for Emergency Use of Pemgarda (Formerly VYD222) for Pre-exposure Prophylaxis (PrEP) of COVID-19" (Press release). Invivyd. 22 March 2024. Archived from the original on 23 March 2024. Retrieved 23 March 2024 – via GlobeNewswire.
  5. .

Public Domain This article incorporates public domain material from the United States Department of Health and Human Services