Trial intelligence / Profile preview

TUL321 in Healthy Participants

NCT07760467Phase 1Recruiting

Sponsor
The United Laboratories International Holdings
Start
Aug 2026
Primary completion
May 2027
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in paroxysmal nocturnal hemoglobinuria (PNH) comparing TUL321 with Placebo (2 arms). Primary endpoints: Incidence of adverse events up to 17 days and Changes from baseline in physical examinations, vital signs, electrocardiograms (ECG), and laboratory tests up to 17 days. Started Aug 2026; status: recruiting.

02

Drugs

TUL321
03

Conditions

paroxysmal nocturnal hemoglobinuria (PNH)

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