A Phase 1, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of a SARS-CoV-2-directed Monoclonal Antibody in Healthy Participants
Latest Information Update: 06 Feb 2025
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At a glance
- Drugs VYD 2311 (Primary) ; VYD 2311 (Primary)
- Indications COVID 2019 infections
- Focus Adverse reactions; First in man
- 03 Feb 2025 According to Invivyd media release, trial has fully enrolled, and all planned doses have been administered, with only long-term follow-up remaining.
- 19 Nov 2024 Planned number of patients changed from 30 to 40.
- 19 Nov 2024 Planned End Date changed from 1 Apr 2025 to 1 May 2025.