Ibsrela Patent Expiration

Ibsrela is a drug owned by Ardelyx Inc. It is protected by 5 US drug patents filed from 2019 to 2024 out of which none have expired yet. Ibsrela's patents have been open to challenges since 13 September, 2023. Based on its patents and exclusivities, its generic launch date is estimated to be Aug 01, 2033. Details of Ibsrela'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.
US8541448 Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
Aug, 2033

(8 years from now)

Active
US8969377 Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
Dec, 2029

(5 years from now)

Active
US12016856 Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
Dec, 2029

(5 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).
US9006281 Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
May, 2030

(5 years from now)

Active
US9408840 Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorder
Dec, 2029

(5 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 Ibsrela's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 8th Yr, Small Entity 09 Feb, 2024 US9408840
Payment of Maintenance Fee, 8th Yr, Small Entity 14 Oct, 2022 US9006281
Patent Term Extension Certificate 06 Oct, 2022 US8541448
Payment of Maintenance Fee, 8th Yr, Small Entity 06 Sep, 2022 US8969377
Notice of Final Determination -Eligible 20 Jul, 2022 US8541448
Notice of Final Determination -Eligible 14 Jul, 2022 US8541448
FDA Final Eligibility Letter 17 Feb, 2022 US8541448
Payment of Maintenance Fee, 8th Yr, Small Entity 24 Mar, 2021 US8541448
transaction for FDA Determination of Regulatory Review Period 08 Feb, 2021 US8541448
Second letter to regulating agency to determine regulatory review period 15 Jul, 2020 US8541448


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

Exclusivity Information

Ibsrela holds 1 exclusivities. All of its exclusivities have expired in 2024. Details of Ibsrela's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Sep 12, 2024

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

Ibsrela's Family Patents

Ibsrela has patent protection in a total of 21 countries. It's US patent count contributes only to 31.1% of its total global patent coverage. 1 country has all of their patents expired or invalidated which has opened up potential generic launch opportunities in this particular country. Click below to unlock the full patent family tree for Ibsrela.

Family Patents

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Generic Launch

Generic Release Date:

Ibsrela's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Aug 01, 2033 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Ibsrela Generics:

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

Alternative Brands for Ibsrela

Ibsrela which is used for treating irritable bowel syndrome with constipation., has several other brand drugs using the same active ingredient (Tenapanor Hydrochloride). Given below is the list of those companies and their brand drugs, to help you identify new opportunities, assess competitors, and plan your market strategies more effectively.

Drug Owner Drug Name
Ardelyx Inc
Xphozah






About Ibsrela

Ibsrela is a drug owned by Ardelyx Inc. It is used for treating irritable bowel syndrome with constipation. Ibsrela uses Tenapanor Hydrochloride as an active ingredient. Ibsrela was launched by Ardelyx Inc in 2019.

Approval Date:

Ibsrela was approved by FDA for market use on 12 September, 2019.

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 Ibsrela is 12 September, 2019, its NCE-1 date is estimated to be 13 September, 2023.

Active Ingredient:

Ibsrela uses Tenapanor Hydrochloride as the active ingredient. Check out other Drugs and Companies using Tenapanor Hydrochloride ingredient

Treatment:

Ibsrela is used for treating irritable bowel syndrome with constipation.

Dosage:

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

Strength Dosage Form Availability Application Pathway
EQ 50MG BASE TABLET Prescription ORAL