A Study to Learn About the Study Medicine NURTEC® ODT 75 mg After it is Released Into the Markets in Korea
← catalyst calendarNCT07497854 · readout in 1,441 d
Sponsored by Pfizer (industry) · PFE — their whole pipeline →.
Phase
—
Status
Not yet recruiting
Study type
Observational
Enrollment
3,000estimated
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-10-01 | estimated | When the study began enrolling |
| Primary completion | 2030-07-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2030-08-01 | estimated | The whole study's end, after follow-up |
| First posted | 2026-03-27 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-15 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Migraine With or Without Aura
Intervention
- Drug: Rimegepant sulfate
Primary outcomes
what the primary-completion date above is the date OFTo evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
To evaluate the safety of NURTEC® ODT 75 mg (Rimegepant sulfate) in adult patients with acute treatment of migraine with or without aura and with preventive treatment of episodic migraine.
measured 28 days after from last administration of NURTEC® ODT 75 mg (Rimegepant sulfate)
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