Viewing Study NCT01862367

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Ignite Modification Date: 2025-12-25 @ 10:49 PM

Study NCT ID: NCT01862367

Status: COMPLETED

Last Update Posted: 2019-07-09

First Post: 2013-05-21

Is NOT Gene Therapy: False

Has Adverse Events: False

Brief Title: Use of rFXIII in Treatment of Congenital FXIII Deficiency, a Prospective Multi-centre Observational Study

Sponsor: Novo Nordisk A/S

Organization:

Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Study Modules

Identification Module Status Module Sponsor Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms Interventions Module Outcomes Module Eligibility Module Contacts Locations Module References Module