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NCT02116712
Phase 1Interventional
Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.
View on ClinicalTrials.gov ↗Timeline
- Start date
- Aug 1, 2014
- Primary completion
- Jun 1, 2015
- Completion date
- Jul 1, 2015
- First posted
- —
- Last posted
- —
- Enrollment
- 9
- Arms / groups
- 1 / —
- Source
- AACT · pre-existing
Sponsors
- Baylor UniversityLead sponsor
- University of CincinnatiOverall official - principal investigator
- University of Texas at HoustonOverall official - principal investigator
- Baylor UniversityOverall official - principal investigator
- Baylor UniversityStudy chair
- Baylor UniversitySponsor investigator
- University of CincinnatiCollaborator
- The University of Texas, DallasCollaborator
Drugs studied
Indications studied
CDEK-curated fields only — the ClinicalTrials.gov results mirror (baseline measures, adverse events, participant flow) is a separate, currently-dormant pipeline; see MIGRATION_PLAN.md.