At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 40 enrolled
Drug / intervention
Dexanabinol Dose Level 1 +5 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Assessment of Safety, Tolerability and Pharmacokinetics of Single Doses of Oral Dexanabinol in Healthy Subjects
In Brief
A Phase 1 clinical trial evaluating Dexanabinol Dose Level 1, Dexanabinol Dose Level 2, and 4 other interventions for Safety and 3 related conditions. Completed, enrolled 40 participants across 1 site.
Detailed Summary
The purpose of this study is to test the safety and observe the pharmacokinetics (distribution and elimination of the drug) of the compound dexanabinol (ETS2101) in healthy male subjects following a single oral dose.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSafety, Tolerability, Pharmacokinetics, Cancer
CountriesUnited Kingdom
Collaborators--
Timeline
Phase 1CompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartJan 2014
First PostedFeb 2014
Primary CompletionSep 2014
TodayJul 2026
First PostedFeb 4, 2014
Enrollment StartJan 1, 2014
Primary CompletionSep 1, 2014
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 12.4 years ago
Interventions
Dexanabinol Dose Level 1drug
Oral formulation of dexanabinol
Dexanabinol Dose Level 2drug
Oral formulation of dexanabinol
Dexanabinol Dose Level 3drug
Oral formulation of dexanabinol
Dexanabinol Dose Level 4drug
Oral formulation of dexanabinol
Dexanabinol Dose Level 5drug
Oral formulation of dexanabinol
Placebodrug