Status:

COMPLETED

Food-Effect Pharmacokinetic Study of PL2200

Lead Sponsor:

PLx Pharma

Conditions:

Healthy

Eligibility:

All Genders

21-65 years

Phase:

PHASE1

Brief Summary

This trial is a food-effect study to assess fasted versus fed pharmacokinetics of PL2200.

Eligibility Criteria

Inclusion

  • Healthy normal male and female volunteers between 21 and 65 years of age.

Exclusion

  • Abnormal findings on physical examination or clinical laboratories, or significant medical history.
  • Subject with hypersensitivity or contraindications to aspirin, ibuprofen, or other nonsteroidal anti-inflammatory drug (NSAID).

Key Trial Info

Start Date :

October 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT01244100

Start Date

October 1 2010

Last Update

December 13 2010

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Houston Institute for Clinical Research

Houston, Texas, United States, 77074