TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

NULIBRY

FOSDENOPTERIN HYDROBROMIDE
Approved 2021-02-26
2
Indications
--
Phase 3 Trials
1
Priority Reviews
5
Years on Market

Details

Status
Prescription
First Approved
2021-02-26
Routes
INTRAVENOUS
Dosage Forms
POWDER

Companies

Active Ingredient: FOSDENOPTERIN HYDROBROMIDE

NULIBRY Approval History

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What NULIBRY Treats

1 indications

NULIBRY is approved for 1 conditions since its original approval in 2021. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Molybdenum Cofactor Deficiency
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.

NULIBRY FDA Label Details

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Indications & Usage

FDA Label (PDF)

NULIBRY is indicated to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCD) Type A. NULIBRY is cyclic pyranopterin monophosphate (cPMP) indicated to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCD) Type A.

NULIBRY Patents & Exclusivity

Latest Patent: Apr 2029
Exclusivity: Feb 2028

Patents (1 active)

US7504095 Expires Apr 9, 2029

Exclusivity

NCE Until Feb 2026
ODE-342 Until Feb 2028
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.