Active, not recruitingEarly Phase 1NCT06892301
Clinical Exploration Study of YOLT-203 in the Treatment of Type 1 Primary Hyperoxaluria (PH1)
Studying Primary hyperoxaluria
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
- Guangzhou Women and Children's Medical Center
- Principal Investigator
- Wenhao Zhou, PhD, MD, M.DGuangzhou Women and Children's Medical Center
- Intervention
- YOLT-203(drug)
- Enrollment
- 2 enrolled
- Eligibility
- 2-18 years · All sexes
- Timeline
- 2025 – 2026
Study locations (1)
- Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, China
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.
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