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NCT01161654 · ClinicalTrials.gov registry record · NA

Bioequivalency Study of Naratriptan Hydrochloride 2.5 mg Under Fed Conditions

A NA study of Migraine, sponsored by Roxane Laboratories.

Completed
Registry status
NA
Development phase
33
Enrollment target
1
Study location

NCT01161654: Completed NA study of Migraine, sponsored by Roxane Laboratories.

NCT01161654 is a NA study of Migraine that has completed, run by Roxane Laboratories. The registered enrollment target is 33 participants, below the 358-participant average among 102 other Migraine trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01161654, a NA study of Migraine, has completed, sponsored by Roxane Laboratories.

COMPLETED
Registry status
NA
Development phase
33 participants
Enrollment target
1
Study location

Study Summary

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

Conditions Studied

Interventions

  • DRUG naratriptan hydrochoride

Study Locations (1)

Washington

  • Charles River Northwest Kinetics - Tacoma

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2007-08
Est. Completion 2007-09
Phase NA
Roxane Laboratories

93 total trials

What the finished NCT01161654 record still lists

NCT01161654 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 358-participant average among 102 other Migraine trials with a reported enrollment target (91% lower).

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 1 intervention - of which naratriptan hydrochoride is the first listed.

NCT01161654 reports a single indexed study location in Washington.

Frequently Asked Questions

What is clinical trial NCT01161654 about?

NCT01161654 is a clinical study titled "Bioequivalency Study of Naratriptan Hydrochloride 2.5 mg Under Fed Conditions". The objective of this study was to prove the bioequivalence of Naratriptan Hydrochloride Tablet under fed conditions.

What is the current status of trial NCT01161654?

This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2007-08. Estimated completion is 2007-09.

What conditions does trial NCT01161654 study?

This clinical trial studies the following conditions: Migraine.

What interventions are being tested in trial NCT01161654?

The interventions under investigation include: naratriptan hydrochoride (DRUG).

Who is sponsoring clinical trial NCT01161654?

This trial is sponsored by Roxane Laboratories, which has 93 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01161654 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Migraine

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01161654's enrollment target sits among peer trials

33 90th of 102 higher than 13 of 102 other Migraine trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Migraine trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01161654, the US trial registry maintained by the National Library of Medicine. NCT01161654 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.