A Phase 1b, Single Center, Clinical Study to Investigate the Safety and Biological Responses to Baminercept in Patients With Chronic HCV Hepatitis.
1 other identifier
interventional
N/A
1 country
1
Brief Summary
Erstes Safety Trial mit Baminercept in chronischen HCV Patienten. Untersuchung des potentiell antiviralen, antiinflammatorischen Effekts sowie Modulation der hepatischen Gen-Expression. 10 Patienten, open label, 10 Wochen Therapie. Sequentielles Enrollement der ersten 4 Patienten.
- Trial with medicinal product
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Oct 2010
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 8, 2010
CompletedFirst Posted
Study publicly available on registry
July 16, 2010
CompletedStudy Start
First participant enrolled
October 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2013
CompletedJuly 16, 2010
July 1, 2010
July 8, 2010
July 15, 2010
Conditions
Outcome Measures
Primary Outcomes (1)
Sicherheit
Interventions
Eligibility Criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Zurichlead
- PD Dr. rer. nat. Mathias Heikenwäldercollaborator
Study Sites (1)
Unknown Facility
Zurich, Switzerland
MeSH Terms
Interventions
Study Officials
- STUDY DIRECTOR
01 Studienregister MasterAdmins
UniversitaetsSpital Zuerich
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 8, 2010
First Posted
July 16, 2010
Study Start
October 1, 2010
Study Completion
February 1, 2013
Last Updated
July 16, 2010
Record last verified: 2010-07