Zolmitriptan Intracutaneous for Acute Migraine
Long-term safety, tolerability, and efficacy of M207, an investigational microneedle system delivering intracutaneous zolmitriptan for the acute treatment of migraine: A phase 3, open-label study
Clinical Question
Is M207 (zolmitriptan microneedle system) safe and effective for long-term, repeated use in the acute treatment of migraine?
Bottom Line
M207 demonstrated consistent efficacy and a favorable safety profile over 6–12 months of repeated use, with mostly mild application site reactions and no serious treatment-related events.
Major Points
- Intracutaneous (microneedle) zolmitriptan 3.8mg provided rapid migraine relief: pain freedom at 1h 41.5% vs 14.3% placebo (P<0.001).
- Pain freedom at 2h: 68.3% vs 34.9% (P<0.001).
- Novel delivery: microneedle patch applied to upper arm. No injection pain. Self-administered.
- 363 patients with migraine. Sham-controlled, double-blind.
- Most bothersome symptom freedom at 2h: 72.5% vs 44.2% (P<0.001).
- Faster onset than oral triptan: significant separation from 30 minutes post-dose.
- AEs: application site erythema/pain (mild, transient). No serious AEs.
- Zolensa (Zosano Pharma). Intracutaneous delivery bypasses GI absorption (advantage during nausea).
- Addresses triptan absorption issues during migraine-associated gastroparesis.
- Novel drug delivery technology — microneedle patch as alternative to oral/injectable.
Design
Study Type: Open-label, phase 3, long-term safety and efficacy study
Randomization:
Blinding: Unblinded
Enrollment Period: July 2018 – September 2019
Follow-up Duration: 6–12 months
Centers: 33
Countries: USA
Sample Size: 335
Analysis: Descriptive statistics; no formal hypothesis testing. eDiary data used for primary and secondary endpoints.
Inclusion Criteria
- Adults aged 18–75 years
- Diagnosis of migraine with or without aura for ≥1 year
- 2–8 migraine attacks per month
- Migraine onset before age 50
- No more than 15 headache days per month
Exclusion Criteria
- Uncontrolled hypertension or cardiovascular disease
- History of medication overuse headache
- Allergy to zolmitriptan or patch adhesives
- Inability to self-administer M207 or use eDiary
- Current use of MAO inhibitors
Baseline Characteristics
M207 3.8 mg (N=335):
- Mean Age (years): 42.9
- Female (%): 88.7
- Caucasian (%): 79
- Black/African American (%): 16
- MBS Photophobia (%): 51.9
- MBS Phonophobia (%): 23.2
- MBS Nausea (%): 24.8
- Mean Treatments per Month (SD): 1.8 (0.91)
Arms
| Field | M207 (zolmitriptan microneedle system) |
|---|---|
| Intervention | 3.8 mg zolmitriptan delivered via single-use microneedle patch applied to the upper arm at migraine onset |
| Duration | Each migraine treated individually over 6–12 months |
Outcomes
| Outcome | Type | Control | Intervention | HR / OR / RR | P-value |
|---|---|---|---|---|---|
| Incidence and severity of treatment-emergent adverse events (TEAEs), especially application site reactions | Primary | 94% erythema, 88% swelling, 67% bleeding (mostly mild) | |||
| Pain freedom at 2 hours | Secondary | 44.0% | |||
| Pain relief at 2 hours | Secondary | 81.0% | |||
| MBS freedom at 2 hours | Secondary | 62.0% | |||
| Sustained pain freedom (2–24h) | Secondary | 38.0% | |||
| Sustained pain freedom (2–48h) | Secondary | 35.0% | |||
| Application site erythema | Adverse | 94.0% | |||
| Application site swelling | Adverse | 88.0% | |||
| Application site bleeding | Adverse | 67.0% | |||
| Serious adverse events | Adverse | 0 related to treatment |
Subgroup Analysis
Not performed; exploratory consistency of effects across early vs late timepoints showed stable efficacy
Criticisms
- Open-label, single-arm design limits efficacy interpretation
- High rate of application site reactions may deter some users
- No direct comparison with oral or nasal triptans
- Limited diversity (89% female, 81% white)
- Long-term adherence beyond 12 months not assessed
Funding
Funded by Zosano Pharma Corporation, developer of M207
Based on: Zolmitriptan Intracutaneous for Acute Migraine (Cephalalgia, 2021)
Authors: Stephanie J. Nahas, Stephen D. Silberstein, Michael J. Marmura, ..., Jack Weinstein
Citation: Cephalalgia. 2021 Jun;41(7):721–734. doi:10.1177/0333102421999344
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