← Back to Treatments
🏅 FDA Orphan Designation

Kalbitor

ECALLANTIDE

Manufacturer: Takeda Pharmaceuticals America, Inc.

Indicated for:
Hereditary angioedema
⚠️

Black Box Warning (Boxed Warning)

A Boxed Warning is the FDA's strongest safety warning — it indicates serious or life-threatening risks identified during clinical trials or post-market surveillance. It does not mean the medication is unsafe for all patients; your prescriber weighs these risks against the benefits for your specific situation. Source: FDA-approved prescribing information.

View full prescribing information on DailyMed (NLM) ↗

FDA-Approved Indications (1)

indicated for treatment of acute attacks of hereditary angioedema (HAE) in patients 12 years of age and older

Population: pediatric ≥12 years and older

Indications & Usage

1 INDICATIONS AND USAGE KALBITOR ® (ecallantide) is indicated for treatment of acute attacks of hereditary angioedema (HAE) in patients 12 years of age and older. KALBITOR is a plasma kallikrein inhibitor indicated for treatment of acute attacks of hereditary angioedema (HAE) in patients 12 years of age and older. ( 1 )

💙 Support Programs

View all →
Kalbitor
Takeda
Apply ↗
Kalbitor
Takeda Pharmaceuticals America, Inc.
Apply ↗

Where shown, WAC (Wholesale Acquisition Cost) is an estimate only — your actual cost depends on your insurance plan. Always verify pricing with your pharmacy or insurer.

Medical disclaimer: This information is for educational purposes only. Always consult a qualified healthcare provider before making treatment decisions. Data sourced from FDA and current as of our last update.