RecruitingNCT01257269

Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)

Studying Congenital thrombotic thrombocytopenic purpura

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Key facts

Sponsor
Insel Gruppe AG, University Hospital Bern
Principal Investigator
Johanna A Kremer Hovinga, MD
University Clinic of Hematology and Central Hematology Laboratory, Bern University Hospital and the University of Bern, Inselspital
Intervention
Observation(other)
Enrollment
450 enrolled
Eligibility
All sexes
Timeline
20062030

Study locations (7)

Collaborators

Swiss National Science Foundation · Mach Gaensslen Foundation · Baxalta Innovations GmbH, Wien, Austria

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 NCT01257269 on ClinicalTrials.gov

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