Active, not recruitingPhase 1NCT04058756
Rollover Study for Continued Safety and Tolerability in Subjects Treated With Spartalizumab Alone or in Combination With Other Study Treatments
Studying Hinman syndrome
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
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- PDR001(drug)
- Enrollment
- 120 target
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2019 – 2030
Study locations (30)
- Columbia University Medical Center, New York, New York, United States
- Providence Portland Medical Center, Portland, Oregon, United States
- MD Anderson Cancer Center Uni of Te, Houston, Texas, United States
- Novartis Investigative Site, Leuven, Belgium
- Novartis Investigative Site, Liège, Belgium
- Novartis Investigative Site, Toronto, Ontario, Canada
- Novartis Investigative Site, Montreal, Quebec, Canada
- Novartis Investigative Site, Guangzhou, Guangdong, China
- Novartis Investigative Site, Guangzhou, China
- Novartis Investigative Site, Brno, Czechia
- Novartis Investigative Site, Lille, France
- Novartis Investigative Site, Lyon, France
- Novartis Investigative Site, Marseille, France
- Novartis Investigative Site, Villejuif, France
- Novartis Investigative Site, Jena, Thuringia, Germany
- +15 more locations on ClinicalTrials.gov
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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