A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of ADG20 in the Treatment of Ambulatory Participants with Mild or Moderate COVID-19 (STAMP)
Latest Information Update: 10 May 2024
At a glance
- Drugs Adintrevimab (Primary)
- Indications COVID 2019 infections
- Focus Adverse reactions; Proof of concept; Registrational; Therapeutic Use
- Acronyms STAMP
- Sponsors Invivyd
- 07 May 2024 According to an Invivyd media release, company announced its intention to submit an emergency use authorization (EUA) application to the U.S. Food and Drug Administration (FDA) for pemivibart for the treatment of mild to moderate symptomatic COVID-19 in certain immunocompromised people utilizing a rapid immunobridging pathway based on data from Phase 2/3 clinical trial (STAMP) and CANOPY Phase 3 clinical trial.
- 22 Nov 2022 Status changed from active, no longer recruiting to discontinued.
- 13 Nov 2022 This trial has been Discontinued in Germany, According to European Clinical Trials Database record.