A Study to Evaluate the Long-Term Safety of M207 in the Acute Treatment of Migraine
Status: | Active, not recruiting |
---|---|
Conditions: | Migraine Headaches |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 2/2/2019 |
Start Date: | November 7, 2017 |
End Date: | March 2019 |
A Long-Term, Open-Label Study to Evaluate the Safety of M207 (Zolmitriptan Intracutaneous Microneedle System) in the Acute Treatment of Migraine
This is an open-label, twelve-month safety study. There is a screening period followed by a
run-in period to record migraine activity. Qualified subjects will receive study medication
for up to twelve months for the treatment of multiple migraine attacks. Using the eDiary to
confirm they are experiencing a qualified migraine, subjects will self-administer the patches
and respond to questions in the eDiary post treatment administration.
run-in period to record migraine activity. Qualified subjects will receive study medication
for up to twelve months for the treatment of multiple migraine attacks. Using the eDiary to
confirm they are experiencing a qualified migraine, subjects will self-administer the patches
and respond to questions in the eDiary post treatment administration.
This is an open-label, twelve-month safety study. There is a screening period followed by a
run-in period (14 to 21 days) to determine eligibility for treatment with study medication
based on daily eDiary data collection. Qualified subjects will receive study medication on
Day 1 for up to twelve months for the treatment of migraine headaches. Migraines will be
treated with a single dose, consisting of two patches, but subjects can treat multiple
migraine attacks throughout the 12 months. Using the eDiary to confirm they are experiencing
a qualified migraine, subjects will self-administer the patches and continue to respond to
questions in the eDiary for 48 hours post treatment administration.
run-in period (14 to 21 days) to determine eligibility for treatment with study medication
based on daily eDiary data collection. Qualified subjects will receive study medication on
Day 1 for up to twelve months for the treatment of migraine headaches. Migraines will be
treated with a single dose, consisting of two patches, but subjects can treat multiple
migraine attacks throughout the 12 months. Using the eDiary to confirm they are experiencing
a qualified migraine, subjects will self-administer the patches and continue to respond to
questions in the eDiary for 48 hours post treatment administration.
Main Inclusion Criteria:
1. Women or men 18 to 75 years of age
2. Greater than 1 year history of episodic, migraine (with or without aura) with onset
prior to 50 years of age.
3. Migraine history during the prior 6 months must include:
1. at least 2 migraines per month
2. no more than 8 migraines per month
3. no more than 15 headache days per month
4. Women of child-bearing potential must not be pregnant, must agree to avoid pregnancy
and use an acceptable double-barrier method of birth control during the trial.
5. Willing and able to treat a minimum of 2 migraines per month with study medication and
consistently complete eDiary for up to 12 months.
Main Exclusion Criteria:
1. Contraindication to triptans
2. Use of SSRIs (drugs like Prozac®) or SNRIs (drugs like Effexor®) or anti-coagulants
(drugs like Coumadin®)
3. Known allergy or sensitivity to zolmitriptan or its derivatives or formulations
4. Known allergy or sensitivity to adhesives and/or titanium
5. Women who are pregnant, breast-feeding or plan a pregnancy during this study
6. Three or more of the following cardiovascular risk factors:
- Current tobacco use
- Hypertension or receiving anti-hypertensive medication for hypertension
- Hyperlipidemia or on prescribed anti-cholesterol treatment
- Family history of premature coronary artery disease
- Diabetes mellitus
7. History or current abuse or dependence on alcohol or drugs
We found this trial at
31
sites
Los Angeles, California 90017
Principal Investigator: Salil Nadkarni, MD
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2017 Canyon Road, Suite 41
Birmingham, Alabama 35216
Birmingham, Alabama 35216
(205) 757-8208

Principal Investigator: Hayes Williams, MD
Site Overview Achieve has two clinical research sites in Birmingham, AL. Our Birmingham sites are conveniently located...
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Anderson, South Carolina 29621
Principal Investigator: Erin Cooksey, MD
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Ann Arbor, Michigan 48104
Principal Investigator: Joel Saper, MD
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Dallas, Texas 75390
Principal Investigator: Deborah Friedman, MD
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Denver, Colorado 80230
Principal Investigator: Shaila Gogate, MD
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8001 West 26th Avenue
Hialeah, Florida 33016
Hialeah, Florida 33016
Principal Investigator: Juan Fernandez, MD
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HIgh Point, North Carolina 27262
Principal Investigator: Thomas Jarrett, MD
Phone: 336-883-9773
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1 Medical Center Dr
Lebanon, New Hampshire 03756
Lebanon, New Hampshire 03756
(603) 650-5000

Principal Investigator: Stewart Tepper, MD
Dartmouth Hitchcock Medical Center Dartmouth-Hitchcock is a national leader in patient-centered health care and building...
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Minneapolis, Minnesota 55402
Principal Investigator: Gary Berman, MD
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Mount Pleasant, South Carolina 29464
Principal Investigator: Cynthia Strout, MD
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New Braunfels, Texas 78130
Principal Investigator: Frank Hampel Jr., MD
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Palo Alto, California 94304
Principal Investigator: Nada Hindiyeh, MD
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1020 Walnut St
Philadelphia, Pennsylvania 19107
Philadelphia, Pennsylvania 19107
(215) 955-6000

Principal Investigator: Stephanie Nahas-Geiger, MD
Thomas Jefferson University We are dedicated to the health sciences and committed to educating professionals,...
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Plymouth, Minnesota 55441
Principal Investigator: Hemalini Mehta, MD
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Raleigh, North Carolina 27607
Principal Investigator: Craig LaForce, MD
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Raleigh, North Carolina 27609
Principal Investigator: John Rubino, MD
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Rochester, New York 14609
Principal Investigator: Matthew Davis, MD
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3862 Mexico Road
Saint Peters, Missouri 63303
Saint Peters, Missouri 63303
Principal Investigator: Timothy Smith, MD
Phone: 636-387-5100
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San Jose, California 95117
Principal Investigator: James Wolfe, MD
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Santa Monica, California 90404
Principal Investigator: David Kudrow, MD
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Watertown, Massachusetts 02472
Principal Investigator: Egilius Spierings, MD
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