CompletedPhase 4NCT01467947
Postmarketing Immunogenicity Study in HAE Subjects Treated With Berinert
Studying Hereditary angioedema
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
- CSL Behring
- Principal Investigator
- Mikhail RojavinCSL Behring
- Intervention
- Berinert, lyophilizate for IV application containing 500 IU C1-INH to be reconstituted with 10 mL water for injection(biological)
- Enrollment
- 46 enrolled
- Eligibility
- 12 years · All sexes
- Timeline
- 2011 – 2014
Study locations (4)
- MHAT "Tsaritsa Yoanna", Sofia, Bulgaria
- Semmelweis University, Budapest, Hungary
- Jagiellonian University, Krakow, Krakow, Poland
- Spitalul Clinic Judeţean Mureş,Secţia Clinică Medicină Internă,Compartimentul Alergologie şi Imunologie, Târgu-Mures, Mureș County, Romania
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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