Active, not recruitingPhase 1NCT04954001
Study to Evaluate the Safety, Tolerability, PK Characteristics and Anti-tumor Activity of FCN-159 in Adult and Pediatric Participants With Neurofibromatosis Type 1
Studying Neurofibromatosis type 1
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
- Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.
- Intervention
- FCN-159(drug)
- Enrollment
- 160 enrolled
- Eligibility
- 2-70 years · All sexes
- Timeline
- 2021 – 2025
Study locations (14)
- Children's Hospital Los Angeles, Los Angeles, California, United States
- Principal Investigator Hans, Gainesville, Florida, United States
- John Hopkins All Children Hospital, St. Petersburg, Florida, United States
- Henry Ford Health System, Detroit, Michigan, United States
- Medical University of South Carolina - Hollings Cancer Center - PPDS, Charleston, South Carolina, United States
- Research Site, Beijing, China
- Research Site, Guangzhou, China
- Research Site, Hangzhou, China
- Research Site, Shanghai, China
- Research Site, Shijiazhuang, China
- Research Site, Wuhan, China
- Hospital Universitario Vall d'Hebron, Barcelona, Spain
- Hospital Universitario 12 de Octubre, Madrid, Spain
- Hospital Universitario La Paz, Madrid, Spain
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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