FOXP1

Clinical trial pipeline · Data from ClinicalTrials.gov

See which FOXP1 trials you may qualify for

Total trials

Actively recruiting

Phase 3 trials

Completed

Trial phase breakdown

Trial status

Actively recruiting — 2 trials

RecruitingNot Applicable

NCT01238250

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders a…

United States100,000 participantsStarted 2010-10

RecruitingNot Applicable

NCT03718923

FOXP1 Syndrome: The Seaver Autism Center for Research and Treatment is Characterizing FOXP1-related Neurodevelopmental D…

FOXP1, also known as Forkhead-box Protein P1, is a transcription factor protein belonging to the FOX gene family. Disruptions in the FOXP1 gene cause a phenotyp…

United States50 participantsStarted 2016-03-28

All recent trials (3 shown)

CompletedNot Applicable

NCT06211673

Psychiatric Phenotype Characterization of Individuals With FOXP1 Syndrome

FOXP1 syndrome is a rare genetic disorder with a variable phenotype, characterized somatically by facial dysmorphia, dysphagia, hypotonia, relative or real macr…

France25 participantsStarted 2024-01-19

Treatment: Semi-structured interviews, Heteroquestionnaires