CompletedNot applicableNCT05051657
Evaluation of the Express Plus Range
Studying Homocystinuria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Vitaflo International, Ltd
- Principal Investigator
- Anita MacDonaldBirmingham Women's and Children's Hospital
- Intervention
- PKU express plus(dietary_supplement)
- Enrollment
- 28 enrolled
- Eligibility
- 3 years · All sexes
- Timeline
- 2021 – 2026
Study locations (6)
- Royal Belfast Hospital for Sick Children, Belfast, United Kingdom
- Birmingham Women's and Children's Hospital, Birmingham, United Kingdom
- Bristol Royal Hospital for Children, Bristol, United Kingdom
- Greater Glasgow and Clyde NHS Foundation Trust, Glasgow, United Kingdom
- Great Ormond Street Hospital for Children, London, United Kingdom
- Nottingham Children's Hospital, Nottingham, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05051657 on ClinicalTrials.govOther trials for Homocystinuria
Additional recruiting or active studies for the same condition.
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- ACTIVE NOT RECRUITINGNANCT06495567Proof of Concept Creatine Supplementation for Homocystinuria StudyUniversity of British Columbia
- ENROLLING BY INVITATIONPHASE3NCT06431893A Phase 3 Long-term Extension Study to Assess the Long-term Safety and Efficacy of Pegtibatinase Treatment in Participants ≥5 to ≤65 Years of Age With Classical Homocystinuria (HCU) (ENSEMBLE)Travere Therapeutics, Inc.
- ACTIVE NOT RECRUITINGPHASE3NCT06247085A Study to Investigate Efficacy and Safety of Pegtibatinase Compared With Placebo in Participants ≥12 to ≤65 Years of Age With Classical Homocystinuria (HCU) Due to Cystathionine Beta Synthase Deficiency Receiving Standard of Care TreatmentTravere Therapeutics, Inc.
- ACTIVE NOT RECRUITINGPHASE1, PHASE2NCT03406611Pegtibatinase As an Enzyme Therapy for Patients with Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (COMPOSE)Travere Therapeutics, Inc.
- RECRUITINGNCT02998710Natural History Study of Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (ACAPPELLA)Travere Therapeutics, Inc.