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Completed Phase 3 Interventional

An Efficacy Study of a Single Dose Treatment of PRO-513 for Subjects Suffering a Migraine Attack

ClinicalTrials.gov ID: NCT00330850

Public ClinicalTrials.gov record NCT00330850. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to show the efficacy of a single dose of PRO-513 for treating subjects suffering moderate pain form a migraine attack, with or without aura. The study is also intended to show the effectiveness of PRO-513 for associated symptoms of nausea, photophobia, and phonophobia due to a migraine attack.

Study identification

NCT ID
NCT00330850
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ProEthic Pharmaceuticals
Industry
Enrollment
650 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2006 (Type not available)
Primary completion
Not listed
Completion
Dec 2006 (Type not available)
Last update posted
Apr 2, 2007

2006

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Associated Neurologists of Southern CT Fairfield Connecticut 06824 —
New England Center for Headache Stamford Connecticut 06902 —
LCFP Inc. Fort Myers Florida 33907 —
Palm Beach Neurological Center Palm Beach Gardens Florida 33410 —
Diamond Headache Clinic Chicago Illinois 60614 —
International Research Center Towson Maryland 21286 —
Michigan Head-Pain and Neurologic Institute Ann Arbor Michigan 48104 —
Mercy Health Research St Louis Missouri 63141 —
New York Headache Center New York New York 10021 —
Headache Wellness Center Greensboro North Carolina 27401 —
DermResearch, Inc. Austin Texas 78759 —
J&S Studies, Inc. Bryan Texas 77802 —
Houston Headache Clinic Houston Texas 77004 —
Road Runner Research, Ltd. San Antonio Texas 78258 —
The Innovative Clinical Research Center Alexandria Virginia 22304 —
Advanced Healthcare, S.C. Milwaukee Wisconsin 53209 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00330850, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 2, 2007 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00330850 live on ClinicalTrials.gov.

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