Bioequivalency Study of Naratriptan Hydrochloride 2.5 mg Under Fasted Conditions

Completed · Not applicable

Conditions studied: Migraine

In brief

The objective of this study was to prove the bioequivalence of Naratriptan Hydrochloride Tablet under fasted conditions.

Key facts

Study ID

NCT01161667

Run by

Roxane Laboratories

People needed

35

Starts

2007-09-01

Expected to finish

2007-09-01

Last updated by the study team

2018-01-23

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening

You may not qualify if…

• Positive test for HIV, Hepatitis B, or Hepatitis C.
• Treatment with known enzyme altering drugs.
• History of allergic or adverse response to naratriptan hydrochloride or any comparable or similar product.

Where it is running

• Charles River Northwest Kinetics — Tacoma, Washington, United States

Full record on ClinicalTrials.gov

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