Skip to main content
OpenTrials
Completed

NCT Number: NCT03282227

A Study to Evaluate the Long-Term Safety of M207 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 electronic diary (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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

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

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Achieve Clinical Research, Birmingham, Alabama, United States

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Main Inclusion Criteria:

  • Women or men 18 to 75 years of age
  • Greater than 1 year history of episodic, migraine (with or without aura) with onset prior to 50 years of age.
  • Migraine history during the prior 6 months must include:
  • at least 2 migraines per month
  • no more than 8 migraines per month
  • no more than 15 headache days per month
  • 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.
  • 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:

  • Contraindication to triptans
  • Use of selective serotonin reuptake inhibitors (drugs like Prozac®) or serotonin or norepinephrine reuptake inhibitors (drugs like Effexor®) or anti-coagulants (drugs like Coumadin®)
  • Known allergy or sensitivity to zolmitriptan or its derivatives or formulations
  • Known allergy or sensitivity to adhesives and/or titanium
  • Women who are pregnant, breast-feeding or plan a pregnancy during this study
  • 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
  • History or current abuse or dependence on alcohol or drugs

Treatment and study plan

M207 Microneedle System

Drug

M207 Microneedle System 3.8 mg

Other names: ZP-Zolmitriptan Intracutaneous Microneedle System, ADAM-Zolmitriptan

Primary outcomes

  1. Number of Subjects With Any Treatment-emergent Adverse Events (TEAE) Over 12 Months

    Time frame: 0 to 12 months

    Number and % of subjects in safety population with any treatment-emergent adverse event(s) during the study. TEAE is defined as any new adverse event (AE) that started after first patch application. This was an open-label study with no control group. No statistical analyses were performed. Application site skin reactions including erythema, swelling, haemorrhage, bruise, pain, and pruritus were collected systematically via subject e-diary and/or investigator skin assessment at study visits. All other AEs were spontaneously reported by subject or observed upon examination.

Secondary outcomes

  1. Percentage of Migraine Attacks for Which Pain Freedom Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of migraine attacks for which pain freedom defined as a pain level of 'None' (Grade 0 on pain severity scale where 0: None, 1: Mild, 2: Moderate, 3: Severe, and lower values represent a better outcome) was achieved at 2 hours post-dose without the use of rescue medication. This was an open-label study with no control group. No statistical analyses were performed.

  2. Percentage of Migraine Attacks for Which Most Bothersome Symptom Freedom Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of migraine attacks for which freedom from most bothersome symptom other than pain defined as an absence of the most bothersome symptom was achieved at 2 hours post-dose without the use of rescue medication. This was an open-label study with no control group. No statistical analyses were performed.

  3. Percentage of Migraine Attacks for Which Pain Relief Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of migraine attacks for which pain relief defined as an improvement of pain severity (1) to mild (Grade 1) or none (Grade 0) from moderate (Grade 2) or severe (Grade 3) at baseline, or (2) an improvement of pain severity to none (Grade 0) from mild (Grade 1) at baseline, without rescue medication was achieved. Pain severity scale has grades: 0: None, 1: Mild, 2: Moderate, 3: Severe, where lower values represent a better outcome. This was an open-label study with no control group. No statistical analyses were performed.

  4. Percentage of Migraine Attacks for Which Nausea Freedom Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of subjects for which nausea freedom defined as absence of nausea and/or vomiting without the use of rescue medication was achieved at 2 hours post-dose. This was an open-label study with no control group. No statistical analyses were performed.

  5. Percentage of Migraine Attacks for Which Photophobia Freedom Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of migraine attacks for which photophobia freedom defined as an absence of photophobia without the use of rescue medication was achieved at 2 hours post-dose. This was an open-label study with no control group. No statistical analyses were performed.

  6. Percentage of Migraine Attacks for Which Phonophobia Freedom Was Achieved at 2 Hours Post-dose

    Time frame: 2 hours for each Migraine, up to 12 months for each subject

    Percentage of migraine attacks for which phonophobia freedom defined as an absence of phonophobia without the use of rescue medication was achieved at 2 hours post-dose. This was an open-label study with no control group. No statistical analyses were performed.

Sponsors and collaborators

Lead sponsor

Zosano Pharma Corporation

Industry

Registry information

Official study title

A Long-Term, Open-Label Study to Evaluate the Safety of M207 (Zolmitriptan Intracutaneous Microneedle System) in the Acute Treatment of Migraine

Acronym: ADAM

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Sep 13, 2017
Registry last updated
Aug 19, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.