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The Effect of Sumatriptan and Placebo on CGRP Induced Headache

The Effect of Sumatriptan and Placebo on CGRP Induced Headache

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03542357
Enrollment
30
Registered
2018-05-31
Start date
2018-02-15
Completion date
2018-09-01
Last updated
2019-09-12

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

Conditions

Migraine

Brief summary

To develop a pragmatic migraine model the investigators will induce headache in healthy volunteers and in patients with migraine without aura with aCalcitonine Gene Related Peptide (CGRP). If the headache responds to sumatriptan, the model can be used to test new drug candidates.

Detailed description

There remains a great need for more effective anti-migraine drugs with fewer side effects. Human experimental models are valuable in early phase development of new anti-migraine drugs but useful models have not yet been developed. The investigators' group has shown that Calcitonine Gene Related Peptide (CGRP) induce headache/migraine in both healthy volunteers and in patients with migraine without aura (MO). To validate this model, the headache must respond to specific migraine treatment with sumatriptan. Hypothesis: CGRP induces a migraine-like headache in both healthy subjects and in MO-patients and induced headache responds to a specific anti migraine drug; sumatriptan. Aim: Developing a pragmatic and valid model for the testing of new anti-migraine drugs.

Interventions

DRUGCalcitonin Gene Related Peptide

CGRP is given both study days to induce headache. One day the headache is treated with placebo and the other day with sumatriptan

CGRP is given both study days to induce headache. One day the headache is treated with placebo and the other day with sumatriptan

DRUGPlacebo Oral Tablet

CGRPis given both study days to induce headache. One day the headache is treated with placebo and the other day with sumatriptan

Sponsors

Danish Headache Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy: Healthy subjects of both sexes Age 18-60 years Weight 45-95 kg. Females were requested to use effective contraception. Migraine patients: Migraine patients who meet IHS criteria for migraine with or without aura of both sexes 18-60 years 45-95 kg.

Exclusion criteria

Healthy: Any type of headache (except episodic tension-type headache \< 1 day per week) Serious somatic or psychiatric disease Pregnancy Intake of daily medication (except oral contraceptives). Migraine patients: Any other type of headache then migraine without aura (except episodic tension-type headache \< 1 day per week) Serious somatic or psychiatric disease Pregnancy Intake of daily medication (except oral contraceptives) Triptan non-responders

Design outcomes

Primary

MeasureTime frameDescription
AUC after infusion1 yearThe investigators will assess the outcome measures 1 year after the beginning of the study

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026