Wednesday, July 8, 2026

Drug profile · INN

suzetrigine

suzetrigine (JOURNAVX) is an FDA-listed pharmaceutical active ingredient. Associated with Vertex Pharmaceuticals (Australia) Pty.. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 1
Pipeline programs 8
News articles 4
Drug details — suzetrigine

Quick answer

suzetrigine (JOURNAVX) is an FDA-listed pharmaceutical active ingredient. Associated with Vertex Pharmaceuticals (Australia) Pty.. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN suzetrigine
Brand JOURNAVX
Route ORAL
Formulation TABLET

Approval history

Authority Status Date
FDA approved

Recent coverage

Lilly buys 4E in non-opioid pain push: what investors should watch
High impact Analysismoderate to severe acute painJun 16, 2026

Lilly buys 4E in non-opioid pain push: what investors should watch

FDA · moderate to severe acute pain · 6 min

Eli Lilly is buying 4E Therapeutics, adding another non-opioid pain pipeline to its portfolio after the SiteOne transaction. The move comes as Journavx (suzetrigine) advances in the market and in multiple clinical trials.

Dr. Sarah Mitchell
FDA approves Vertex’s Journavx as first non-opioid pain drug for acute pain
High impact Analysismoderate-to-severe acute painJun 7, 2026

FDA approves Vertex’s Journavx as first non-opioid pain drug for acute pain

FDA · moderate-to-severe acute pain · 7 min

The FDA approved Vertex Pharmaceuticals’ Journavx (suzetrigine) on 30 January 2025 for moderate-to-severe acute pain in adults. The decision creates a new non-opioid catalyst to track for BD teams, investors, and analysts.

Dr. Sarah Mitchell
FDA Approves Vertex’s First-in-Class Non-Opioid Pain Drug Journavx
Critical impact Analysismoderate-to-severe acute painJun 7, 2026

FDA Approves Vertex’s First-in-Class Non-Opioid Pain Drug Journavx

FDA · moderate-to-severe acute pain · 8 min

The FDA approved Journavx (suzetrigine) on 30 January 2025 for moderate-to-severe acute pain in adults, including postoperative pain. The decision gives Vertex the first non-opioid analgesic in this setting and creates a new catalyst set for BD teams, investors, and analysts.

Dr. Sarah Mitchell
Vertex launches Journavx after FDA approval for acute pain
High impact AnalysisoncologyJun 7, 2026

Vertex launches Journavx after FDA approval for acute pain

FDA · oncology · 9 min

Vertex’s Journavx (suzetrigine) became the first FDA-approved non-opioid analgesic for moderate to severe acute pain on January 30, 2025. This plan frames the catalyst, label, and upcoming clinical milestones for BD teams, investors, and analysts.

Dr. Sarah Mitchell

Pipeline programs

  1. SUZ Phase 3 · Vertex Pharmaceuticals (Australia) · Acute Pain
  2. Suzetrigine Phase 3 · Vertex Pharmaceuticals (Australia) · Diabetic Peripheral Neuropathic Pain
  3. Suzetrigine (SUZ) Phase 3 · Vertex Pharmaceuticals (Australia) · Acute Pain
  4. Suzetrigine Phase 2 · Vertex Pharmaceuticals (Australia) · Diabetic Peripheral Neuropathy
  5. SUZ Phase 1 · Vertex Pharmaceuticals (Australia) · Pain
  6. Suzetrigine Approved · Vertex Pharmaceuticals (Australia) · Acute Pain
  7. Suzetrigine Approved · Vertex Pharmaceuticals (Australia) · Pain
  8. suzetrigine Approved · Vertex Pharmaceuticals (Australia) · Pain, Acute Postoperative
  1. US 11834441

    Substituted tetrahydrofurans as modulators of sodium channels

    Expires Mon Nov 30 2043 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is suzetrigine?

suzetrigine (JOURNAVX) is an FDA-listed pharmaceutical active ingredient. Associated with Vertex Pharmaceuticals (Australia) Pty.. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for suzetrigine?

JOURNAVX is a marketed brand name for suzetrigine. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of suzetrigine?

suzetrigine has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.