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NCT Number: NCT04743141

Long-term Safety Study of Rimegepant in Pediatric Subjects for the Acute Treatment of Migraine

The purpose of this study is to test the long-term safety of rimegepant in the acute treatment of migraine in children and adolescents (≥ 6 to < 18 years of age).

Recruiting

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Key information

Age range

6 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

NZOZ Wielospecjalistyczna Poradnia Lekarska SYNAPSIS, Lech Szczechowski, Katowice, Poland

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • History of migraine (with or without aura) for ≥ 6 months before Screening.
  • History of 1 to 8 moderate or severe attacks per month during the 2 months prior to screening.
  • 1 or more migraine days requiring treatment during the Observation Phase.
  • Prophylactic migraine medication is permitted if the dose has been stable for at least 12 weeks prior to the Screening Visit.
  • Ability to distinguish between migraine and other types of headaches.
  • Weight > 15 kg. For EU countries only: Participants 12 to < 18 years of age must have a body weight of >25kg.
  • Adequate venous access for blood sampling.
  • Male and female participants 6 to < 18 years of age (participants must not reach their 18th birthday on or before the Baseline visit).

Exclusion criteria

  • History of cluster headache or hemiplegic migraine headache.
  • Confounding and clinically significant pain syndrome.
  • Current uncontrolled and/or untreated psychiatric condition for a minimum of 6 months prior to the Screening Visit (lifetime history of psychosis and/or mania are excluded).
  • History of suicidal behavior or at risk of self-harm/harm to others.
  • History of major psychiatric disorder.
  • Current diagnosis or history of substance abuse
  • Reported current use of or tested positive at Screening for drugs of abuse.

Treatment and study plan

Rimegepant (PF-07899801)

Drug

Rimegepant 75 mg, 50 mg or 35 mg ODT

Primary outcomes

  1. The frequency and severity of on-treatment and treatment-emergent adverse events, serious adverse events, adverse events leading to discontinuation, clinically significant lab abnormalities

    Time frame: 58 weeks

    To evaluate the safety and tolerability of rimegepant in children and adolescents (6 to < 18 years of age).

Secondary outcomes

  1. The frequency and severity of hepatic-related adverse events and frequency of hepatic-related adverse events leading to treatment discontinuation

    Time frame: 58 weeks

    To evaluate the frequency and severity of hepatic-related adverse events and the frequency of hepatic-related treatment discontinuations in children and adolescents (6 to less than 18 years of age) treated with rimegepant.

Study contacts

Contact information is provided by the study sponsor or research team.

Pfizer Pfizer CT.gov Call Center

CONTACT

[email protected]

1-800-718-1021

Sponsors and collaborators

Lead sponsor

Pfizer

Industry

Registry information

Official study title

Phase 3, Multicenter, Open-label Study to Assess the Long-term Safety and Tolerability of Rimegepant for the Acute Treatment of Migraine (With or Without Aura) in Children and Adolescents ≥ 6 to < 18 Years of Age

Important dates

Study start
2021
Primary completion
2030
Study completion
2030
First posted
Feb 8, 2021
Registry last updated
Jul 30, 2026

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.

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