CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 26 enrolled
Drug / intervention
GSK2838232 100 mg tablet +3 moredrug
Likely dose
GSK2838232 100 mg tabletfrom 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.

Search/NCT03234036
NCT03234036Phase 1Completed

A Two Part Study to Assess i) the Relative Bioavailability and Food Effect of a Novel Tablet Formulation of Boosted-GSK2838232 Compared to Capsule and ii) the Safety and Pharmacokinetics of Repeated Once-Daily Doses of Non-boosted GSK2838232

GlaxoSmithKline·interventional·Posted Jul 31, 2017·Updated Oct 28, 2020

In Brief

A Phase 1 clinical trial evaluating GSK2838232 100 mg tablet, GSK2838232 50 mg capsule, and 2 other interventions for Infection, Human Immunodeficiency Virus and HIV Infections. Completed, enrolled 26 participants across 1 site.

Detailed Summary

This study will be conducted in two Parts to confirm the acceptability/selection of a tablet formulation for future clinical development of GSK2838232. Part 1 of the study will assess single ritonavir (RTV)-boosted doses of a new tablet formulation given with food (containing approximately 30% fat) against the reference capsule formulation also given with food and then will assess the impact of fasted conditions on the tablet performance. In Part 2, non-boosted GSK2838232 will be given as once-daily tablet doses for 11 days in a separate group of subjects, assuming the tablet performance is considered acceptable from Part 1. Approximately 16 healthy subjects will be enrolled to provide at least 12 evaluable subjects through the three study periods in Part 1. 10 healthy subjects will be enrolled to provide at least 8 evaluable subjects through the single study period in Part 2. The maximum duration of study participation will be approximately 9 to 10 weeks for Part 1; and 8 to 9 weeks for Part 2.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
201820192020202120222023202420252026
First PostedJul 31, 2017
Enrollment StartAug 2, 2017
Primary CompletionNov 10, 2017
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 8.9 years ago

Interventions

GSK2838232 100 mg tabletdrug

It is a white to slightly colored tablet. It will be supplied as prefilled tablets in bulk for dispensing to subjects at the site according to the treatment code.

GSK2838232 50 mg capsuledrug

It is a pink unmarked capsule. It will be supplied as prefilled capsules in bulk for dispensing to subjects at the site according to the treatment code.

Ritonavir 100 mg tabletsdrug

It is a white film-coated ovaloid tablets.

Placebo for GSK2838232 tabletsdrug

It is a white to slightly colored tablet. The placebo tablets supplied will not be identical to GSK2838232 tablets. It will be administered by site staff via an opaque card or paper tube.