TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

QALSODY

TOFERSEN
Approved 2023-04-25
1
Indication
--
Phase 3 Trials
1
Priority Reviews
2
Years on Market

Details

Status
Prescription
First Approved
2023-04-25
Routes
INTRATHECAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: TOFERSEN

QALSODY Approval History

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What QALSODY Treats

1 indications

QALSODY is approved for 1 conditions since its original approval in 2023. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Amyotrophic Lateral Sclerosis
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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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.

QALSODY FDA Label Details

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Indications & Usage

FDA Label (PDF)

QALSODY is indicated for the treatment of amyotrophic lateral sclerosis (ALS) in adults who have a mutation in the superoxide dismutase 1 ( SOD1 ) gene. This indication is approved under accelerated approval based on reduction in plasma neurofilament light chain (NfL) observed in patients treated with QALSODY [see Clinical Studies ] . Continued approval for this indication may be contingent upon verification of clinical benefit in confirmatory trial(s). QALSODY is an antisense oligonucleotide indicated for the treatment of amyotrophic lateral sclerosis (ALS) in adults who have a mutation in th...

QALSODY Patents & Exclusivity

Latest Patent: Mar 2035
Exclusivity: Apr 2030

Patents (3 active)

US10968453 Expires Apr 1, 2035
US10669546 Expires Apr 1, 2035
US10385341 Expires Apr 1, 2035

Exclusivity

NCE Until Apr 2028
ODE-432 Until Apr 2030
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.