Inluriyo Patent Expiration

Inluriyo is a drug owned by Eli Lilly And Co. It is protected by 2 US drug patents filed in 2025 out of which none have expired yet. Inluriyo's patents will be open to challenges from 25 September, 2029. Based on its patents and exclusivities, its generic launch date is estimated to be Jul 11, 2039. Details of Inluriyo's patents and their expiration are given in the table below.

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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.
US10654866 Selective Estrogen Receptor Degraders
Jul, 2039

(13 years from now)

Active
US11117902 Selective Estrogen Receptor Degraders
Jul, 2039

(13 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 Inluriyo's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 4th Year, Large Entity 20 Feb, 2025 US11117902
Payment of Maintenance Fee, 4th Year, Large Entity 20 Oct, 2023 US10654866
Patent Issue Date Used in PTA Calculation 14 Sep, 2021 US11117902
Recordation of Patent Grant Mailed 14 Sep, 2021 US11117902
Email Notification 26 Aug, 2021 US11117902
Issue Notification Mailed 25 Aug, 2021 US11117902
Dispatch to FDC 09 Aug, 2021 US11117902
Application Is Considered Ready for Issue 09 Aug, 2021 US11117902
Issue Fee Payment Received 06 Aug, 2021 US11117902
Issue Fee Payment Verified 06 Aug, 2021 US11117902


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

Exclusivity Information

Inluriyo holds 1 exclusivities out of which none have expired. Its last outstanding exclusivity is set to expire in 2030. Details of Inluriyo's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Sep 25, 2030

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

Inluriyo's Family Patents


Family Patents

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Generic Launch

Generic Release Date:

Inluriyo's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Jul 11, 2039 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Inluriyo Generics:

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





About Inluriyo

Inluriyo is a drug owned by Eli Lilly And Co. Inluriyo uses Imlunestrant Tosylate as an active ingredient. Inluriyo was launched by Eli Lilly in 2025.

Approval Date:

Inluriyo was approved by FDA for market use on 25 September, 2025.

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 Inluriyo is 25 September, 2025, its NCE-1 date is estimated to be 25 September, 2029.

Active Ingredient:

Inluriyo uses Imlunestrant Tosylate as the active ingredient. Check out other Drugs and Companies using Imlunestrant Tosylate ingredient

Dosage:

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

Strength Dosage Form Availability Application Pathway
EQ 200MG BASE TABLET Prescription ORAL


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