TheraRadar

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Data updated: Mar 10, 2026

ANDEMBRY

GARADACIMAB-GXII
Approved 2025-06-16

Andembry (garadacimab-gxii) is a monoclonal antibody indicated for the prevention of hereditary angioedema (HAE) attacks. The treatment is approved for use in adult and pediatric patients aged 12 years and older. It serves as a prophylactic therapy to reduce the frequency of the inflammatory swelling episodes associated with this condition.

Source: FDA Label β€’ CSL BEHRING LLC

How ANDEMBRY Works

Garadacimab-gxii functions by binding to and inhibiting activated Factor XII (FXIIa), the initial factor in the contact activation pathway. This inhibition prevents the conversion of prekallikrein to kallikrein and subsequently reduces the generation of bradykinin. By lowering bradykinin levels, the drug limits the biological processes that cause inflammation and swelling during HAE attacks.

Source: FDA Label
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-06-16
Routes
SUBCUTANEOUS
Dosage Forms
INJECTABLE

Companies

Active Ingredient: GARADACIMAB-GXII

ANDEMBRY Approval History

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What ANDEMBRY Treats

1 indications

ANDEMBRY is approved for 1 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Hereditary Angioedema
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.

ANDEMBRY FDA Label Details

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Indications & Usage

FDA Label (PDF)

ANDEMBRY is indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients aged 12 years and older. ANDEMBRY is an activated Factor XII (FXIIa) inhibitor (monoclonal antibody) indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients aged 12 years and older.

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Data Sources

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