TheraRadar

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Data updated: Mar 10, 2026

ZEMBRACE SYMTOUCH

SUMATRIPTAN SUCCINATE
Neurology Approved 2016-01-28
2
Indications
--
Phase 3 Trials
10
Years on Market

Details

Status
Prescription
First Approved
2016-01-28
Routes
SUBCUTANEOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: SUMATRIPTAN SUCCINATE

ZEMBRACE SYMTOUCH Approval History

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What ZEMBRACE SYMTOUCH Treats

1 indications

ZEMBRACE SYMTOUCH is approved for 1 conditions since its original approval in 2016. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Migraine
Source: FDA Label

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ZEMBRACE SYMTOUCH FDA Label Details

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Indications & Usage

FDA Label (PDF)

ZEMBRACE SymTouch is indicated for the acute treatment of migraine with or without aura in adults. ZEMBRACE SymTouch is a serotonin (5-HT 1B/1D ) receptor agonist (triptan) indicated for: Acute treatment of migraine with or without aura in adults. Limitations of Use : Use only if a clear diagnosis of migraine has been established. Not indicated for the prophylactic therapy of migraine. Limitations of Use : Use only if a clear diagnosis of migraine has been established. If a patient has no response to the first migraine attack treated with ZEMBRACE SymTouch, reconsider the diagnosis before ZEMB...

ZEMBRACE SYMTOUCH Patents & Exclusivity

Latest Patent: Jan 2036

Patents (3 active)

US10537554 Expires Jan 29, 2036
US11364224 Expires Jan 29, 2036
US12097183 Expires Jan 29, 2036
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.