TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

LETYBO

LETIBOTULINUMTOXINA-WLBG Acetylcholine Release Inhibitors
Approved 2024-02-29

LETYBO (letibotulinumtoxinA-wlbg) is an acetylcholine release inhibitor and neuromuscular blocking agent. It is indicated for the temporary improvement in the appearance of moderate to severe glabellar lines in adult patients. The treatment specifically targets lines associated with the activity of the corrugator and/or procerus muscles. Its therapeutic role is to provide a temporary reduction in muscle activity in the localized area of injection.

Source: FDA Label • HUGEL INC • Acetylcholine Release Inhibitor

How LETYBO Works

LETYBO blocks cholinergic transmission at the neuromuscular junction by inhibiting the release of the neurotransmitter acetylcholine. Once injected, the drug enters the nerve terminal and cleaves SNAP25, a protein necessary for the release of acetylcholine into the synapse. This process results in a dose-dependent decrease in muscle function. Muscle activity gradually returns as the neurotoxin degrades and the nerves form axonal sprouts to reinnervate the muscle.

Source: FDA Label
1
Indication
--
Phase 3 Trials
2
Years on Market

Details

Status
Prescription
First Approved
2024-02-29
Routes
N/A
Dosage Forms
POWDER, FOR SOLUTION

Companies

Active Ingredient: LETIBOTULINUMTOXINA-WLBG

LETYBO Approval History

Loading approval history...

What LETYBO Treats

1 indications

LETYBO is approved for 1 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Glabellar Lines
Source: FDA Label

LETYBO Boxed Warning

DISTANT SPREAD OF TOXIN EFFECT The effects of all botulinum toxin products, including LETYBO, may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. LETYBO is not approved for the treatment of spasticity or any conditions other than glabellar lines [see Warnings and Precautions ( 5.1 )] . ...

🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

Loading...
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.

LETYBO FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

LETYBO is indicated for the temporary improvement in the appearance of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult patients. LETYBO is an acetylcholine release inhibitor and a neuromuscular blocking agent indicated for the temporary improvement in the appearance of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult patients.

⚠️ BOXED WARNING

WARNING: DISTANT SPREAD OF TOXIN EFFECT The effects of all botulinum toxin products, including LETYBO, may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficu...

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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