TerminatedPHASE1, PHASE2NCT02566603
PRTX-100-203 Open-Label, Dose Escalation Study in Adult Patients With ITP
Studying Autoimmune thrombocytopenia
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
- Protalex, Inc.
- Principal Investigator
- William E Gannon, MDProtalex, Inc.
- Intervention
- PRTX-100(drug)
- Enrollment
- 15 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2018
Study locations (16)
- Haut-Levêque Hospital, Pessac, Bordeaux, France
- CH Lyon Sud, Pierre-Bénite, Lyon, France
- Côte de Nacre Hospital, Caen, France
- Mondor Hospital, Créteil, France
- University Hospital, Dijon, France
- Claude Huriez Hospital, Lille, France
- CH La Timone, Marseille, France
- CHU, Nantes, France
- Canceropole, Toulouse, France
- Hammersmith Hospital, London, OHS, United Kingdom
- UCLH, London, UK, United Kingdom
- Guy's and St. Thomas Hospital, London, UK, United Kingdom
- St. Georges' Hospital, London, UK, United Kingdom
- Derriford Hospital, Plymouth, UK, United Kingdom
- University Hospital Southampton, Southampton, UK, United Kingdom
- +1 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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