Isturisa Patent Expiration

Isturisa is a drug owned by Recordati Rare Diseases Inc. It is protected by 6 US drug patents filed in 2020 out of which none have expired yet. Isturisa's patents have been open to challenges since 06 March, 2024. Based on its patents and exclusivities, its generic launch date is estimated to be Oct 12, 2035. Details of Isturisa'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.
US9434754 Use of an adrenal hormone-modifying agent
Jan, 2031

(6 years from now)

Active
US8314097 Organic compounds
Mar, 2029

(4 years from now)

Active
US8835646 Organic compounds
Aug, 2026

(1 year, 7 months from now)

Active
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US10709691 Pharmaceutical dosage forms
Oct, 2035

(10 years from now)

Active
US10143680 Pharmaceutical dosage forms
Jul, 2035

(10 years from now)

Active
US8609862 Use of an adrenal hormone-modifying agent
Jan, 2031

(6 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 Isturisa's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 12th Year, Large Entity 20 May, 2024 US8314097
Email Notification 13 Mar, 2024 US9434754
Recordation of Patent eCertificate of Correction 12 Mar, 2024 US9434754
Patent eCofC Notification 12 Mar, 2024 US9434754
Mail Patent eCofC Notification 12 Mar, 2024 US9434754
Payment of Maintenance Fee, 8th Year, Large Entity 06 Mar, 2024 US9434754
transaction for FDA Determination of Regulatory Review Period 29 Feb, 2024 US8314097
transaction for FDA Determination of Regulatory Review Period 29 Feb, 2024 US8609862
transaction for FDA Determination of Regulatory Review Period 23 Feb, 2024 US8609862
transaction for FDA Determination of Regulatory Review Period 23 Feb, 2024 US8314097


FDA has granted several exclusivities to Isturisa. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Isturisa, 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 Isturisa.

Exclusivity Information

Isturisa holds 2 exclusivities out of which none have expired. Its last outstanding exclusivity is set to expire in 2027. Details of Isturisa's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Mar 06, 2025
Orphan Drug Exclusivity(ODE-286) Mar 06, 2027

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US patents provide insights into the exclusivity only within the United States, but Isturisa 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 Isturisa's family patents as well as insights into ongoing legal events on those patents.

Isturisa's Family Patents

Isturisa has patent protection in a total of 44 countries. It's US patent count contributes only to 12.5% of its total global patent coverage. 2 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 Isturisa.

Family Patents

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Generic Launch

Generic Release Date:

Isturisa's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Oct 12, 2035 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Isturisa Generics:

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





About Isturisa

Isturisa is a drug owned by Recordati Rare Diseases Inc. It is used for treating Cushing's disease. Isturisa uses Osilodrostat Phosphate as an active ingredient. Isturisa was launched by Recordati Rare in 2020.

Approval Date:

Isturisa was approved by FDA for market use on 06 March, 2020.

NCE-1 date:

NCE-1 date also known as the four year date occurs four years after the original drug approval and marks the first opportunity for a generic manufacturer to file an ANDA with a Paragraph IV certification. This is the earliest point when generic competition might begin, provided the challenge is successful. Since the approval date for Isturisa is 06 March, 2020, its NCE-1 date is estimated to be 06 March, 2024.

Active Ingredient:

Isturisa uses Osilodrostat Phosphate as the active ingredient. Check out other Drugs and Companies using Osilodrostat Phosphate ingredient

Treatment:

Isturisa is used for treating Cushing's disease.

Dosage:

Isturisa is available in tablet form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
EQ 1MG BASE TABLET Prescription ORAL
EQ 5MG BASE TABLET Prescription ORAL
EQ 10MG BASE TABLET Discontinued ORAL