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CompletedNCT04466514

A Phase 1 Study to Evaluate the Effect of Food on Pharmacokinetics of ASTX029

A Phase 1, 3-Way Crossover Study to Evaluate the Effect of Food on Pharmacokinetics of ASTX029

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Astex Pharmaceuticals, Inc. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Open-label, single dose, randomized, three-period, crossover design study to evaluate the effect of food on the bioavailability of a single oral dose of ASTX029 in healthy adult male and female participants. Following a screening period of up to 28 days, eligible participants will be enrolled and randomized to receive a single treatment (A, B, C) in a random order, with each treatment separated by an approximate 5-day washout period. The duration of the study is expected to be approximately 42 days.

Conditions

Interventions

TypeNameDescription
DRUGASTX029Form: tablet; Route of Administration: oral

Timeline

Start date
2020-07-23
Primary completion
2020-10-01
Completion
2020-10-06
First posted
2020-07-10
Last updated
2024-08-02

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04466514. Inclusion in this directory is not an endorsement.

A Phase 1 Study to Evaluate the Effect of Food on Pharmacokinetics of ASTX029 (NCT04466514) · Clinical Trials Directory