Procysbi Patent Expiration

Procysbi is a drug owned by Horizon Therapeutics Usa Inc. It is protected by 25 US drug patents filed from 2013 to 2022 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Feb 16, 2037. Details of Procysbi's patents and their expiration are given in the table below.

Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents protect the active ingredient(API) of the drug. Only drug patent owner can launch products that use this active ingredient until these patents expire.
US9925156 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9925157 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9925158 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US10548859

(Pediatric)

Methods for storing Cysteamine formulations and related methods of treatment
Feb, 2037

(12 years from now)

Active
US10143665

(Pediatric)

Methods for storing cysteamine formulations and related methods of treatment
Feb, 2037

(12 years from now)

Active
US10328037

(Pediatric)

Methods for storing cysteamine formulations and related methods of treatment
Feb, 2037

(12 years from now)

Active
US10905662

(Pediatric)

Methods for storing cysteamine formulations and related methods of treatment
Feb, 2037

(12 years from now)

Active
US10548859 Methods for storing Cysteamine formulations and related methods of treatment
Aug, 2036

(11 years from now)

Active
US10143665 Methods for storing cysteamine formulations and related methods of treatment
Aug, 2036

(11 years from now)

Active
US10328037 Methods for storing cysteamine formulations and related methods of treatment
Aug, 2036

(11 years from now)

Active
US10905662 Methods for storing cysteamine formulations and related methods of treatment
Aug, 2036

(11 years from now)

Active
US9233077

(Pediatric)

Delayed release cysteamine bead formulation, and methods of making and using same
Dec, 2034

(10 years from now)

Active
US9173851

(Pediatric)

Delayed release cysteamine bead formulation, and methods of making and using same
Dec, 2034

(10 years from now)

Active
US9173851 Delayed release cysteamine bead formulation, and methods of making and using same
Jun, 2034

(9 years from now)

Active
US9233077 Delayed release cysteamine bead formulation, and methods of making and using same
Jun, 2034

(9 years from now)

Active
US8026284

(Pediatric)

Enterically coated cystamine, cysteamine and derivatives thereof
Mar, 2028

(3 years from now)

Active
US8026284 Enterically coated cystamine, cysteamine and derivatives thereof
Sep, 2027

(2 years from now)

Active
US9925157

(Pediatric)

Enterically coated cysteamine, cystamine and derivatives thereof
Jul, 2027

(2 years from now)

Active
US9925156

(Pediatric)

Enterically coated cysteamine, cystamine and derivatives thereof
Jul, 2027

(2 years from now)

Active
US9925158

(Pediatric)

Enterically coated cysteamine, cystamine and derivatives thereof
Jul, 2027

(2 years from now)

Active
US9198882

(Pediatric)

Enterically coated cysteamine, cystamine and derivatives thereof
Jul, 2027

(2 years from now)

Active
US9192590

(Pediatric)

Enterically coated cysteamine, cystamine and derivatives thereof
Jul, 2027

(2 years from now)

Active
US9192590 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9925157 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9925158 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US8129433 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9198882 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active
US9925156 Enterically coated cysteamine, cystamine and derivatives thereof
Jan, 2027

(2 years from now)

Active


A patent's expiry date may change depending upon legal activities going on that patent. Critical activities like abandoning of a patent, term extension of a patent or amendment of its claims can increase or decrease the life of a patent hence affecting its expiry date and in turn affecting the generic launch date of that drug. Tracking these ongoing activities on a patent application helps to keep an eye on the latest developments in the patent process of the drug which can give an idea of how early a drug's generic could be available. The next section provides a list of recent legal activities on Procysbi's patents.

Given below is the list of recent legal activities going on the following patents of Procysbi.

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 4th Year, Large Entity 03 Aug, 2023 US10548859
Payment of Maintenance Fee, 8th Year, Large Entity 11 Jul, 2023 US9233077
Payment of Maintenance Fee, 8th Year, Large Entity 01 Jun, 2023 US9198882
Payment of Maintenance Fee, 8th Year, Large Entity 24 May, 2023 US9192590
Payment of Maintenance Fee, 8th Year, Large Entity 03 May, 2023 US9173851
Payment of Maintenance Fee, 12th Year, Large Entity 27 Mar, 2023 US8026284
Payment of Maintenance Fee, 4th Year, Large Entity 27 Dec, 2022 US10328037
Payment of Maintenance Fee, 4th Year, Large Entity 06 Jun, 2022 US10143665
Payment of Maintenance Fee, 4th Year, Large Entity 27 Sep, 2021 US9925156
Payment of Maintenance Fee, 4th Year, Large Entity 27 Sep, 2021 US9925157


FDA has granted several exclusivities to Procysbi. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Procysbi, regardless of the status of it's patents. These exclusivities hence play a crucial role in delaying the generic launch. Given below are details of the exclusivities granted to Procysbi.

Exclusivity Information

Procysbi holds 9 exclusivities out of which 6 have expired. Its last outstanding exclusivity is set to expire in 2025. Details of Procysbi's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Dosage Form(NDF) Apr 30, 2016
New Patient Population(NPP) Aug 14, 2018
Orphan Drug Exclusivity(ODE-45) Apr 30, 2020
M(M-216) Dec 22, 2020
Orphan Drug Exclusivity(ODE) Aug 14, 2022
Orphan Drug Exclusivity(ODE-97) Aug 14, 2022
ODE*(ODE*) Dec 22, 2024
Orphan Drug Exclusivity(ODE-162) Dec 22, 2024
Pediatric Exclusivity(PED) Jun 22, 2025

Stay ahead of others in designing the generic launch strategy of these 5 blockbuster drugs expiring in next 5 years.

Get the exclusive patent insights now. Don't be the last to know.

Several oppositions have been filed on Procysbi's European patents. EP oppositions can significantly impact the timeline for the generic launch of drugs. If an opposition results in the revocation or amendment of a patent, it can shorten the exclusivity period of the original drug. This can lead to an earlier entry of generic versions into the market. To help you estimate the potential early arrival of Procysbi's generic, the next section provides detailed information on ongoing and past EP oppositions related to Procysbi patents.

Procysbi's Oppositions Filed in EPO

Procysbi has faced multiple oppositions in the European Patent Office. The earliest opposition was filed on Sep 18, 2020, by Alfred E. Tiefenbacher (Gmbh & Co. Kg). This opposition was filed on patent number EP12169866A. Click below to reveal the latest opposition data.


Application Filing Date Opposition Party Legal Status
Patent litigations
EP12169866A Sep, 2020 Alfred E. Tiefenbacher (GmbH & Co. KG) Granted and Under Opposition


US patents provide insights into the exclusivity only within the United States, but Procysbi is protected by patents in multiple countries. Understanding the full scope of patent protection is crucial in strategizing market entry. By looking at the broader patent landscape, you can identify markets with weaker patent protection which could be ideal generic entry points. The following section offers details on Procysbi's family patents as well as insights into ongoing legal events on those patents.

Procysbi's Family Patents

Procysbi has patent protection in a total of 33 countries. It's US patent count contributes only to 40.7% of its total global patent coverage. 3 countries have all of their patents expired or invalidated which has opened up potential generic launch opportunities in these countries. Click below to unlock the full patent family tree for Procysbi.

Family Patents

Explore Our Curated Drug Screens

Drugs Generating Over $1 Billion in Annual Revenue
Explore the top-performing drugs that dominate the pharmaceutical industry
View List
NCE-1 Patent Expiry in the Next 1 Year
Identify opportunities as new chemical entity (NCE-1) patents approach expiry
View List
Recently Granted Patents in EP
Find the opportunity to file Oppositions
View List


Generic Launch

Generic Release Date:

Procysbi's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Feb 16, 2037 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Procysbi Generics:

There are no approved generic versions for Procysbi as of now.

How can I launch a generic of Procysbi before its drug patent expiration? :

You can seek FDA approval to launch a generic drug before the expiration of Procysbi's patents related by providing a 'paragraph IV certification' in your application, which states that the patent submitted by the Procysbi's sponsor is invalid, unenforceable, or will not be infringed by your generic product.

Given below are the details of the already filed Para IV certificates on Procysbi -

Strength Submission Date ANDA(s) Filed First applicant approval Last patent expiry 180 day status
25 mg and 75 mg 11 May, 2020 1 16 Aug, 2036
75 mg/Packet and 300 mg/Packet 16 Dec, 2021 1 16 Aug, 2036





About Procysbi

Procysbi is a drug owned by Horizon Therapeutics Usa Inc. It is used for treating nephropathic cystinosis. Procysbi uses Cysteamine Bitartrate as an active ingredient. Procysbi was launched by Horizon in 2013.

Approval Date:

Procysbi was approved by FDA for market use on 30 April, 2013.

Active Ingredient:

Procysbi uses Cysteamine Bitartrate as the active ingredient. Check out other Drugs and Companies using Cysteamine Bitartrate ingredient

Treatment:

Procysbi is used for treating nephropathic cystinosis.

Dosage:

Procysbi is available in the following dosage forms - capsule, delayed release form for oral use, granule, delayed release form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
EQ 25MG BASE CAPSULE, DELAYED RELEASE Prescription ORAL
EQ 75MG BASE CAPSULE, DELAYED RELEASE Prescription ORAL
EQ 300MG BASE/PACKET GRANULE, DELAYED RELEASE Prescription ORAL
EQ 75MG BASE/PACKET GRANULE, DELAYED RELEASE Prescription ORAL