TheraRadar
Data updated: May 26, 2026

ORFADIN (nitisinone)

Hydroxyphenylpyruvate Dioxygenase Inhibitors
Rare Disease Approved 2002-01-18

ORFADIN is indicated for the treatment of Hereditary Tyrosinemia Type 1.

Source: FDA Label • SWEDISH ORPHAN • 4-Hydroxyphenyl-Pyruvate Dioxygenase Inhibitor

How ORFADIN Works

Nitisinone is a competitive inhibitor of 4-hydroxyphenyl-pyruvate dioxygenase, an enzyme upstream of fumarylacetoacetate hydrolase (FAH) in the tyrosine catabolic pathway. By inhibiting this enzyme, it prevents the formation of maleylacetoacetate and fumarylacetoacetate, which otherwise convert to

3
Indications
--
Phase 3 Trials
1
Priority Reviews
24
Years on Market

Details

Status
Prescription
First Approved
2002-01-18
Patent Cliff
2033

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Routes
ORAL
Dosage Forms
SUSPENSION, CAPSULE

Companies

Active Ingredient: NITISINONE

ORFADIN Approval History

2003
2004
2005
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
57 FDA actions from 2002 to 2019 · 1 indication expansions
May 2019 SUPPL
Label · Labeling
Sep 2017 SUPPL
Efficacy
Jun 2017 SUPPL
Label · Labeling

What ORFADIN Treats

1 indications

ORFADIN is approved for 1 conditions since its original approval in 2002. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Hereditary Tyrosinemia Type 1
Source: FDA Label

Drugs Similar to ORFADIN

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1 shared
ETON
Shared indications:
Hereditary Tyrosinemia Type 1
NITYR
NITISINONE
1 shared
CYCLE
Shared indications:
Hereditary Tyrosinemia Type 1
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Clinical Trial Registry

8 trials
Trial Sponsor ID Phase Status Title
NCT01390077 results posted WLN02 Ph 2, Ph 3 completed Nitisinone (NTBC) In Different Age Groups Of Patients With Alkaptonuria
NCT01838655 results posted 130124 13-EI-0124 Ph 1, Ph 2 completed Nitisinone for Type 1B Oculocutaneous Albinism
NCT02750345 results posted CT-003 PXL227430 Ph 1 completed Bioequivalence Study of Two Oral Nitisinone Formulations to Treat Hereditary Tyrosinemia (HT-1)
NCT02750709 results posted CT-001 PXL225418 Ph 1 completed Bioequivalence Study of Two Nitisinone Formulations Compared to Orfadin
NCT02750332 results posted CT-002 PXL225421 Ph 1 completed Bioavailability Food-Effect Study of an Oral Nitisinone Formulation to Treat Hereditary Tyrosinemia (HT-1)
NCT02323529 HT-1 Sobi.NTBC-003 Ph 3 completed Efficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Nitisinone in HT-1
NCT01734889 results posted Sobi.NTBC-002 Ph 1 completed Taste and Palatability of Orfadin Suspension
NCT01828463 SONIA1 UoL000928 Ph 2 completed Dose Response Study of Nitisinone in Alkaptonuria
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Active Pipeline

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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.

ORFADIN FDA Label Details

Indications & Usage

FDA Label (PDF)

ORFADIN is indicated for the treatment of Hereditary Tyrosinemia Type 1.

View full patent landscape →
1 OB patents · 1 families · 35 international docs across 23 countries

ORFADIN Patents & Exclusivity

Latest Patent: Feb 2033

Patents (1 active)

US9301932 Expires Feb 28, 2033
Source: FDA Orange Book

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Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2033
  • 1 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 2 similar drugs
  • Same target/indication analysis
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Data Sources

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