The Safety Of Combo Formulation In The Treatment Of Multiple Episodes Of Acute Migraine Over 12 Months

NCT00442221 | Completed Phase 3 DMC

• 1 other identifier: MT400-303
• Study Type: interventional
• Target: 500
• Locations: 1 country
• Sites: 2

Brief Summary

The objective of this study is to assess the safety of a single-tablet dose of Combo Formulation for the treatment of moderate to severe migraines

Conditions

Migraine Headaches

Keywords

Migrane headaches

Outcome Measures

Primary Outcomes (2)

• END POINTS

• Adverse events, physical examination findings, vital signs and clinical laboratory findings will be evaluated.

Interventions

Sumatriptan and Naproxen sodium DRUG

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subject is a male or a female who is not pregnant or is not lactating. A female is eligible to enter and participate in this study if she is of:
• Non-childbearing potential (i.e., physiologically incapable of becoming pregnant); or,
• Child-bearing potential, has a negative pregnancy test (urine or serum) at screen, and employs one of the following acceptable measures of contraception:
• Complete abstinence from intercourse from 2 weeks prior to administration of the investigational product, throughout the study, and for a time interval after completion or premature discontinuation from the study to account for elimination of the investigational drug (a minimum of 24 hrs); subjects utilizing this method must agree to use an alternate method of contraception if they should become sexually active and will be queried on whether they have been abstinent in the preceding 2 weeks when they present to the clinic for randomized treatment; or,
• Female sterilization; or,
• Sterilization of male partner; or,
• Implants of levonorgestrel; or,
• Injectable progestogen; or,
• Oral contraceptive (combined or progestogen only); or,
• Any intrauterine device (IUD) with published data showing that the lowest expected failure rate is less than 1% per year (not all IUDs meet this criterion); or,
• Any other method with published data showing that the lowest expected failure rate for that method is less than 1% per year.
• Barrier method only if used in combination with any of the above acceptable methods
• Subject is 18 - 65 years of age.
• Subject's first migraine occurred prior to the age of 50 years.
• Subject has at least a 6-month history, immediately prior to screening, of migraine with or without aura according to the International Headache Society criteria (see Appendix I).

You may not qualify if:

• Subject has received another investigational drug within the 4 weeks preceding this study, or subject was enrolled in this study previously.
• Subject has any concurrent medical or psychiatric condition that may affect the interpretation of efficacy and/or safety data or which otherwise contraindicates participation in a clinical trial with a new chemical entity. This includes, but is not limited to, chronic unstable debilitating diseases such as HIV infection, multiple sclerosis, cancer, etc.
• Subject has a clinically significant disorder that, in the opinion of the investigator, would result in the subject's inability to understand and comply with the requirements of the study.
• Subject has a history, symptoms, or signs of ischemic cardiac, cerebrovascular or peripheral vascular syndromes or other significant underlying cardiovascular diseases.
• Subject has a history of cardiac arrhythmias requiring medication or a history of a clinically significant electrocardiogram (ECG) abnormality that, in the investigator's opinion, contraindicates participation in this study.
• Subject has a history of cerebrovascular abnormalities including stroke and/or transient ischemic attacks.
• Subject who, in the investigator's opinion, is likely to have unrecognized cardiovascular disease, based on history or the presence of risk factors (e.g. hypertension, hypercholesterolemia, smoker, obesity, diabetes, strong family history of coronary artery disease, female with surgical or physiological menopause, or male over 40 years of age).
• Subject has evidence or history of ischemic abdominal syndromes, peripheral vascular disease or Raynaud syndrome.
• Subject has uncontrolled hypertension at screening (sitting systolic pressure \>160 millimeters of mercury (mmHg), diastolic pressure \>95 mmHg).
• Subject has a history of epilepsy or conditions associated with a lowered seizure threshold.
• Subject has a history of basilar or hemiplegic migraine.
• Subject has a history of impaired hepatic or renal function that, in the investigator's opinion, contraindicates participation in this study; or the subject has any other abnormal laboratory value of clinical significance for this study.
• Subject has a history of non-migraine (i.e., tension-type, sinus, etc.) headache frequency greater than or equal to 15 days/month in each of the 3 months prior to screening.
• Subject has had \>6 migraine attacks/month in either of the 2 months prior to screening.
• Subject is currently taking a monoamine oxidase inhibitor (MAOI), has taken a MAOI within the 2 weeks prior to screening, or plans to take a MAOI within 2 weeks after treatment.

Sponsors & Collaborators

• POZEN: lead

Study Sites (2)

POZEN Inc.

Chapel Hill, North Carolina, 27517, United States

Location

Headache Wellness Center

Greensboro, North Carolina, 27401, United States

Location

MeSH Terms

Conditions

Migraine Disorders

Interventions

Sumatriptan; Naproxen

Condition Hierarchy (Ancestors)

Headache Disorders, Primary; Headache Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases

Intervention Hierarchy (Ancestors)

Sulfonamides; Amides; Organic Chemicals; Sulfones; Sulfur Compounds; Tryptamines; Indoles; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Naphthaleneacetic Acids; Naphthalenes; Polycyclic Aromatic Hydrocarbons; Hydrocarbons, Aromatic; Hydrocarbons, Cyclic; Hydrocarbons; Polycyclic Compounds

Study Officials

• David Taylor

  POZEN

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Expanded Access: Yes

Study Record Dates

• First Submitted: February 28, 2007
• First Posted: March 1, 2007
• Study Start: May 1, 2004
• Study Completion: August 1, 2004
• Last Updated: March 1, 2007

Record last verified: 2007-02

Locations

US (2)