Clinical trial
POST-MARKETING SURVEILLANCE TO OBSERVE SAFETY AND EFFICACY OF XYNTHA SOLOFUSE PREFILLED SYRINGE
NCT03034044 is registered in ClinicalTrials.gov with Pfizer as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- POST-MARKETING SURVEILLANCE TO OBSERVE SAFETY AND EFFICACY OF XYNTHA SOLOFUSE PREFILLED SYRINGE
- Lead sponsor
- Pfizer
- Phase
- Observational
- Overall status
- Completed
- Start date
- January 31, 2017
- Completion date
- January 17, 2018
- Enrollment
- 106 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
autosomal hemophilia a, classic hemophilia, factor 8 deficiency, congenital, factor viii deficiency, congenital, hemophilia a, congenital