Trial Profile

A Phase 1 Double-Blind, Randomized, Placebo-Controlled, Single Ascending Dose Study to Evaluate Safety, Tolerability, Pharmacokinetics, Immunogenicity and Pharmacodynamics of DF5112 in Healthy Adult Participants

Status: Recruiting

Phase of Trial: Phase I

Latest Information Update: 05 Jun 2026

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At a glance

18 May 2026 According to a Skyhawk Therapeutics Media Release, company announced that the first healthy volunteers have been successfully dosed subcutaneously (SC) with DF5112 following uccessful completion of the intravenous (IV) dosing phase.
18 May 2026 Early results presented in a Skyhawk Therapeutics Media Release
01 Apr 2026 Planned number of patients changed from 64 to 48.

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