CompletedPHASE1, PHASE2NCT01621256
Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss
Studying Sudden sensorineural hearing loss
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
- Nordmark Arzneimittel GmbH & Co. KG
- Principal Investigator
- Martin Canis, MD PhDDepartment for Otorhinolaryngology, LM University Munich
- Intervention
- Ancrod(drug)
- Enrollment
- 31 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2013 – 2018
Study locations (7)
- Site CZ, Hradec Králové, Czechia
- Site CZ, Prague, Czechia
- Site D, Göttingen, Germany
- Site D, Hamburg, Germany
- Site D, Hanover, Germany
- Site D, Landsberg am Lech, Germany
- Site D, München, Germany
Collaborators
ClinSupport GmbH · MWI Medizinisches Wirtschaftsinstitut GmbH · ProjectPharm s.r.o. · LCR Leading Clinical Research s.r.o. · X-act Cologne Clinical Research GmbH
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 NCT01621256 on ClinicalTrials.govOther trials for Sudden sensorineural hearing loss
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