TerminatedPhase 1NCT02096341
A Phase 1 Pilot Study of the Subcutaneous (s.c.) Route to Facilitate the Administration of RRx-001
Studying Lymphoma
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
- EpicentRx, Inc.
- Principal Investigator
- Jeffrey Infante, MDSCRI Development Innovations, LLC
- Intervention
- RRx-001(drug)
- Enrollment
- 2 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2014 – 2016
Study locations (1)
- Sarah Cannon Research Institute, Nashville, Tennessee, United States
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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