Letairis Patent Expiration

Letairis is a drug owned by Gilead Sciences Inc. It is protected by 9 US drug patents filed from 2013 to 2017. Out of these, 3 drug patents are active and 6 have expired. Letairis's patents have been open to challenges since 16 June, 2011. Based on its patents and exclusivities, its generic launch date is estimated to be Oct 14, 2031. Details of Letairis's patents and their expiration are given in the table below.

Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9549926 Compositions and methods of treating pulmonary hypertension
Oct, 2031

(6 years from now)

Active
US9474752 Method for treating a pulmonary hypertension condition
Dec, 2027

(3 years from now)

Active
US8377933 Method for treating a pulmonary hypertension condition
Dec, 2027

(3 years from now)

Active
USRE42462 Carboxylic acid derivatives, their preparation and use
Jul, 2018

(6 years ago)

Expired
US5840722 Use of carboxylic acid derivatives as drugs
Nov, 2015

(8 years ago)

Expired
US8349843 Carboxylic acid derivatives, their preparation and use
Oct, 2015

(9 years ago)

Expired
US7601730 Carboxylic acid derivatives, their preparation and use
Oct, 2015

(9 years ago)

Expired
US7109205 Carboxylic acid derivatives, their preparation and use
Oct, 2015

(9 years ago)

Expired
US5703017 3-(Het) arylcarboxylic acid derivatives, their preparation and intermediates for their preparation
Dec, 2014

(9 years ago)

Expired


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 Letairis's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 8th Year, Large Entity 10 Jul, 2024 US9549926
Expire Patent 15 Feb, 2021 US8349843
Maintenance Fee Reminder Mailed 31 Aug, 2020 US8349843
Payment of Maintenance Fee, 8th Year, Large Entity 06 Aug, 2020 US8377933
Payment of Maintenance Fee, 4th Year, Large Entity 09 Jul, 2020 US9549926
Expire Patent 22 Oct, 2018 US7109205 (Litigated)
Maintenance Fee Reminder Mailed 30 Apr, 2018 US7109205 (Litigated)
Expire Patent 13 Nov, 2017 US7601730
Patent Issue Date Used in PTA Calculation 24 Jan, 2017 US9549926
Recordation of Patent Grant Mailed 24 Jan, 2017 US9549926


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

Exclusivity Information

Letairis holds 3 exclusivities. All of its exclusivities have expired in 2018. Details of Letairis's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Jun 15, 2012
Orphan Drug Exclusivity(ODE) Jun 15, 2014
New Indication(I-716) Oct 02, 2018

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Several oppositions have been filed on Letairis'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 Letairis's generic, the next section provides detailed information on ongoing and past EP oppositions related to Letairis patents.

Letairis's Oppositions Filed in EPO

Letairis has faced multiple oppositions in the European Patent Office. The earliest opposition was filed on Feb 18, 2016, by Teva Pharmaceutical Industries, Ltd.. This opposition was filed on patent number EP07855065A. Click below to reveal the latest opposition data.


Application Filing Date Opposition Party Legal Status
Patent litigations
EP11833507A Dec, 2017 SANDOZ AG Revoked
EP11833507A Dec, 2017 Zentiva Group, a.s. Revoked
EP11833507A Dec, 2017 Generics (U.K.) Limited Revoked
EP11833507A Dec, 2017 Teva Pharmaceutical Industries Ltd Revoked
EP11833507A Dec, 2017 STADA Arzneimittel AG Revoked
EP11833507A Dec, 2017 Alfred E. Tiefenbacher (GmbH & Co. KG) Revoked
EP07855065A Feb, 2016 Alfred E. Tiefenbacher (GmbH & Co. KG) Revoked
EP07855065A Feb, 2016 TEVA PHARMACEUTICAL INDUSTRIES, LTD. Revoked


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

Letairis's Family Patents

Letairis has patent protection in a total of 26 countries. It's US patent count contributes only to 27.9% of its total global patent coverage. 6 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 Letairis.

Family Patents

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Generic Launch

Generic Release Date:

Letairis's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Oct 14, 2031 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Letairis Generic API suppliers:

Ambrisentan is the generic name for the brand Letairis. 9 different companies have already filed for the generic of Letairis, with Apotex having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Letairis's generic

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

You can seek FDA approval to launch a generic drug before the expiration of Letairis's patents related by providing a 'paragraph IV certification' in your application, which states that the patent submitted by the Letairis'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 Letairis -

Strength Submission Date ANDA(s) Filed First applicant approval Last patent expiry 180 day status
5 mg and 10 mg 09 Feb, 2015 1 28 Mar, 2019 09 Jul, 2018 Extinguished





About Letairis

Letairis is a drug owned by Gilead Sciences Inc. It is used for treating pulmonary arterial hypertension (PAH) in combination with tadalafil by inhibiting endothelin receptors. Letairis uses Ambrisentan as an active ingredient. Letairis was launched by Gilead in 2007.

Approval Date:

Letairis was approved by FDA for market use on 15 June, 2007.

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 Letairis is 15 June, 2007, its NCE-1 date is estimated to be 16 June, 2011.

Active Ingredient:

Letairis uses Ambrisentan as the active ingredient. Check out other Drugs and Companies using Ambrisentan ingredient

Treatment:

Letairis is used for treating pulmonary arterial hypertension (PAH) in combination with tadalafil by inhibiting endothelin receptors.

Dosage:

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

Strength Dosage Form Availability Application Pathway
10MG TABLET Prescription ORAL
5MG TABLET Prescription ORAL