Skip to content

Prestige 2- RimegePant in RElation to obeSiTy in miGainE

Status
Not yet recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521475-31-00
Enrollment
26
Registered
2026-03-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine

Brief summary

- Response or non-response to rimegepant 75 mg or 2x75 mg expressed as percentage in pain freedom or freedom from the most bothersome migraine-associated symptom apart from headache after 2 hours (reported in questionnaire)

Detailed description

- Freedom from photophobia, phonophobia, nausea and pain relief 2 hours after administration of rimegepant in either 75 mg or 2x75 mg during a moderate to severe migraine episode; probability of using rescue medication within 24 hours after the dose; sustained freedom from pain, sustained pain relief, pain relapse 2 hours to 48 hours after the dose - Blood: sex steroid levels, rimegepant concentration, CGRP. parameters: Total body weight, total body water (TBW), free mass (FFM), fat mass (FM), s

Interventions

Sponsors

Konvent Der Barmherzigen Brueder
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
- Response or non-response to rimegepant 75 mg or 2x75 mg expressed as percentage in pain freedom or freedom from the most bothersome migraine-associated symptom apart from headache after 2 hours (reported in questionnaire)

Secondary

MeasureTime frame
- Freedom from photophobia, phonophobia, nausea and pain relief 2 hours after administration of rimegepant in either 75 mg or 2x75 mg during a moderate to severe migraine episode; probability of using rescue medication within 24 hours after the dose; sustained freedom from pain, sustained pain relief, pain relapse 2 hours to 48 hours after the dose - Blood: sex steroid levels, rimegepant concentration, CGRP. parameters: Total body weight, total body water (TBW), free mass (FFM), fat mass (FM), s

Outcome results

None listed

Source: EU CTIS · Data processed: Mar 14, 2026