A Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of BCX17725

Recruiting now · Phase 1 · Has a placebo group

Conditions studied: Netherton Syndrome

In brief

This is a first-in-human, Phase 1/1b, 4-part study that includes the evaluation of safety, tolerability, pharmacokinetics (PK), and immunogenicity of BCX17725 when administered via single and multiple doses in healthy adult participants (Parts 1 and 2), and multiple doses in adult participants with Netherton syndrome (Part 3). In Part 4, the effectiveness, safety, and tolerability of BCX17725 when administered via multiple IV and/or SC doses through 12 weeks will be evaluated in adult and adolescent participants with Netherton syndrome.

Key facts

Study ID
NCT06539507
Run by
BioCryst Pharmaceuticals
People needed
78
Starts
2024-09-26
Expected to finish
2026-12-01
Last updated by the study team
2026-06-16

Who can join

Age: 12 and older, up to 65. Sex: any. Healthy volunteers: accepted.

Where it is running

Full record on ClinicalTrials.gov

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