Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 12:36 AM
NCT ID:
NCT05845567
Brief Summary:
Primary objective:
To assess the potential effect of oral Clarithromycin on the single-dose pharmacokinetics of Givinostat.
Secondary objective:
To assess the safety and tolerability of concomitant administration of Givinostat plus Clarithromycin.
Detailed Description:
This study was planned as a phase I, open-label, 3-part, fixed-sequence, non-randomized study in healthy male and female subjects. The study (Part 2) aimed at assessing the potential effect of Clarythromycin on the single dose pharmacokynetics of Givinostat.
The total duration of Part 2 was divided as follows:
* Screening: up to 21 days.
* Treatment Period: Days 1 to 11.
* Safety follow-up visit: 12±2 days.
Subjects were confined at site from Day -1 to Day 11. On Days 1 and 8, a single dose of 50 mg Givinostat, as oral suspension, was administered 1 hour after the planned morning time of Clarithromycin administration.
From Day 4 to Day 10, clarithromycin 500 mg film-coated tablets were administered twice a day, in the morning and in the evening.
The following assessments were performed:
* Blood collection for pharmacokinetic analysis on Days 1 to 4 and 8 to 11.
* Vital signs measurements on Days 1 and 4 to 10.
* 12-lead ECG on Days 1, 3, 7 and 8.
* Blood collection for laboratory tests (hematology and biochemistry) on Day 3.
Subjects were discharged in the morning of Day 11 after completing end of study procedures.
Study:
NCT05845567
Study Brief:
Protocol Section:
NCT05845567