Paving the way: major study launches to ready STXBP1 treatments for trials
Knowledge-focused
Recruiting now
This study follows 120 people with STXBP1-related disorders—a rare genetic condition causing severe developmental delays and seizures—to better understand how the disease changes over time. Researchers will track symptoms and identify the best ways to measure treatment success, s…
Sponsor: European STXBP1 Consortium • Aim: Knowledge-focused
Last updated May 26, 2026 12:02 UTC