Geneva, April 20 -- International Clinical Trials Registry received information related to the study (NCT07526116) titled 'A First in Human Study to Assess Safety, Tolerability and Pharmacokinetics of a Single Dose of REGN22044 in Healthy Adults' on April 6.

Study Type: Interventional

Study Design: Allocation: Randomized. Intervention model: Sequential Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).

Primary Sponsor: Regeneron Pharmaceuticals

Condition: Healthy Volunteer

Intervention: Drug: REGN22044

Recruitment Status: Not recruiting

Phase: Phase 1

Date of First Enrollment: May 7, 2026

Target Sample Size: 64

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