Pharmacodynamic and Pharmacokinetic Study of PL-ASA
NCT04811625 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2022-04-25
Summary
A randomized, open-label, 2-way crossover pharmacodynamic and pharmacokinetic study of a novel pharmaceutical lipid-aspirin complex formulation (PL-ASA) at an 81 mg dose
Conditions
- Healthy Volunteers
Interventions
- DRUG
-
PL-ASA
Pharmacologic profile of different aspirin formulations
Sponsors & Collaborators
-
PLx Pharma
lead INDUSTRY
Principal Investigators
-
Francesco Franchi, MD · University of Florida
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-04-28
- Primary Completion
- 2021-09-15
- Completion
- 2021-09-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
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