At a glance
ClinicalIndex Comparison RecordEarly Ph 1Completed· 8 enrolled
Drug / intervention
[14C]-benzo[a]pyrene +1 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.
Ultralow Dose PAH Binary Mixture Study
In Brief
A Early Phase 1 clinical trial evaluating [14C]-benzo[a]pyrene and [14C]-benzo[a]pyrene plus phenanthrene for Environmental Exposure. Completed, enrolled 8 participants across 1 site.
Detailed Summary
Evaluation of the pharmacokinetics for \[14C\]-benzo\[a\]pyrene (\[14C\]-BaP) and metabolites in plasma and urine over 48 hours following a 50 ng dose (5.4 nCi) alone or with 1250 ng phenanthrene.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEnvironmental Exposure
CountriesUnited States
Timeline
Early Ph 1CompletedFinished
20192020202120222023202420252026
First PostedAug 2018
Enrollment StartOct 2018
Primary CompletionJan 2024
Study CompletionFeb 2024
TodayJul 2026
First PostedAug 15, 2018
Enrollment StartOct 1, 2018
Primary CompletionJan 1, 2024
Study CompletionFeb 1, 2024
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 7.9 years ago
Interventions
[14C]-benzo[a]pyrenedrug
Oral micro-dose (50 ng) (5.4 nCi)
[14C]-benzo[a]pyrene plus phenanthrenedrug
Oral micro-dose of 50 ng (5.4 nCi) \[14C\]-benzo\[a\]pyrene plus 1250 ng phenanthrene