TheraRadar
Data updated: May 26, 2026

ZYCUBO (copper histidinate)

Rare Disease Approved 2026-01-12

ZYCUBO is a copper replacement therapy used for pediatric patients with Menkes disease. This genetic condition interferes with how the body absorbs copper from food and moves it across the blood-brain barrier, leading to a deficiency. This medication helps these children by providing a usable form of copper to support essential copper-dependent enzymes.

Source: FDA Label • SENTYNL THERAPS INC

How ZYCUBO Works

This medication works by providing a bioavailable source of copper through subcutaneous injections, which allows the mineral to bypass the gastrointestinal tract where absorption is normally blocked in Menkes disease. By delivering copper directly, it helps overcome transport issues caused by ATP7A gene variants and supports the activity of copper-dependent enzymes.

1
Indication
--
Phase 3 Trials
1
Priority Reviews
0
Years on Market

Details

Status
Prescription
First Approved
2026-01-12
Patent Cliff
2033

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Routes
SUBCUTANEOUS
Dosage Forms
POWDER

Companies

Active Ingredient: COPPER HISTIDINATE

ZYCUBO Approval History

Original
New Indication
New Form
Label Update
1 FDA actions from 2026 to 2026
Jan 2026 ORIGINAL Priority
New Drug · Type 1 - New Molecular Entity

What ZYCUBO Treats

1 indications

ZYCUBO is approved for 1 conditions since its original approval in 2026. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Menkes Disease
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.

ZYCUBO FDA Label Details

Indications & Usage

FDA Label (PDF)

ZYCUBO is indicated for the treatment of Menkes Disease.

ZYCUBO Patents & Exclusivity

Exclusivity: Jan 2033

Exclusivity

NCE Until Jan 2031
ODE-520 Until Jan 2033
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.