Mekinist Patent Expiration

Mekinist is a drug owned by Novartis Pharmaceuticals Corp. It is protected by 18 US drug patents filed from 2013 to 2024 out of which none have expired yet. Mekinist's patents will be open to challenges from 22 December, 2024. Based on its patents and exclusivities, its generic launch date is estimated to be Mar 02, 2034. Details of Mekinist'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.
US8703781 Pharmaceutical combination of MEK inhibitor and B-RAF inhibitors
Oct, 2030

(5 years from now)

Active
US7378423 Pyrimidine compound and medical use thereof
May, 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).
US10869869

(Pediatric)

Method of adjuvant cancer treatment
Mar, 2034

(9 years from now)

Active
US10869869 Method of adjuvant cancer treatment
Aug, 2033

(8 years from now)

Active
US8580304

(Pediatric)

Pharmaceutical composition
Jul, 2032

(7 years from now)

Active
US9399021

(Pediatric)

Pharmaceutical composition
Jul, 2032

(7 years from now)

Active
US9271941

(Pediatric)

Pharmaceutical composition
Jul, 2032

(7 years from now)

Active
US9155706

(Pediatric)

Pharmaceutical composition
Jul, 2032

(7 years from now)

Active
US9399021 Pharmaceutical composition
Jan, 2032

(7 years from now)

Active
US8580304 Pharmaceutical composition
Jan, 2032

(7 years from now)

Active
US9271941 Pharmaceutical composition
Jan, 2032

(7 years from now)

Active
US9155706 Pharmaceutical composition
Jan, 2032

(7 years from now)

Active
US8703781

(Pediatric)

Pharmaceutical combination of MEK inhibitor and B-RAF inhibitors
Apr, 2031

(6 years from now)

Active
US8952018

(Pediatric)

Pharmaceutical combination of MEK inhibitor and B-Raf inhibitors
Apr, 2031

(6 years from now)

Active
US8952018 Pharmaceutical combination of MEK inhibitor and B-Raf inhibitors
Oct, 2030

(5 years from now)

Active
US7378423

(Pediatric)

Pyrimidine compound and medical use thereof
Nov, 2027

(3 years from now)

Active
US8835443

(Pediatric)

Pyrimidine compound and medical use thereof
Dec, 2025

(1 year, 24 days from now)

Active
US8835443 Pyrimidine compound and medical use thereof
Jun, 2025

(6 months 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 Mekinist's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 4th Year, Large Entity 05 Jun, 2024 US10869869
Payment of Maintenance Fee, 8th Year, Large Entity 10 Jan, 2024 US9399021
Payment of Maintenance Fee, 8th Year, Large Entity 16 Aug, 2023 US9271941
Payment of Maintenance Fee, 8th Year, Large Entity 29 Mar, 2023 US9155706
Payment of Maintenance Fee, 8th Year, Large Entity 27 Jul, 2022 US8952018
Payment of Maintenance Fee, 8th Year, Large Entity 06 Oct, 2021 US8703781
Payment of Maintenance Fee, 8th Year, Large Entity 28 Apr, 2021 US8580304
Recordation of Patent Grant Mailed 22 Dec, 2020 US10869869
Patent Issue Date Used in PTA Calculation 22 Dec, 2020 US10869869
Email Notification 03 Dec, 2020 US10869869


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

Exclusivity Information

Mekinist holds 18 exclusivities out of which 11 have expired. Its last outstanding exclusivity is set to expire in 2030. Details of Mekinist's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Indication(I-678) Jan 08, 2017
New Chemical Entity Exclusivity(NCE) May 29, 2018
M(M-170) Nov 20, 2018
Orphan Drug Exclusivity(ODE) May 29, 2020
Orphan Drug Exclusivity(ODE-48) May 29, 2020
New Indication(I-745) Jun 22, 2020
Orphan Drug Exclusivity(ODE-57) Jan 08, 2021
New Indication(I-778) Apr 30, 2021
New Indication(I-781) May 04, 2021
M(M-246) Oct 06, 2022
Orphan Drug Exclusivity(ODE-148) Jun 22, 2024
Orphan Drug Exclusivity(ODE-182) Apr 30, 2025
Orphan Drug Exclusivity(ODE-183) May 04, 2025
New Indication(I-895) Jun 22, 2025
Pediatric Exclusivity(PED) Sep 16, 2026
New Indication(I-908) Mar 16, 2026
New Product(NP) Mar 16, 2026
Orphan Drug Exclusivity(ODE-428) Mar 16, 2030

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

Mekinist's Oppositions Filed in EPO

Mekinist has faced multiple oppositions in the European Patent Office. The earliest opposition was filed on Mar 12, 2020, by Generics (Uk) Ltd. This opposition was filed on patent number EP10824148A. Click below to reveal the latest opposition data.


Application Filing Date Opposition Party Legal Status
Patent litigations
EP19174594A May, 2023 Brand Murray Fuller LLP Granted and Under Opposition
EP19174594A May, 2023 STADA Arzneimittel AG Granted and Under Opposition
EP13835019A Jun, 2022 Generics [UK] Limited Granted and Under Opposition
EP13835019A Jun, 2022 Teva Pharmaceutical Industries Ltd Granted and Under Opposition
EP13835019A Jun, 2022 STADA Arzneimittel AG Granted and Under Opposition
EP11849974A Apr, 2021 Generics [UK] Limited Granted and Under Opposition
EP11849974A Apr, 2021 Teva Pharmaceutical Industries Ltd Granted and Under Opposition
EP10824148A Mar, 2020 Teva Pharmaceutical Industries Ltd Opposition rejected
EP10824148A Mar, 2020 Generics (UK) Ltd Opposition rejected


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

Mekinist's Family Patents

Mekinist has patent protection in a total of 45 countries. It's US patent count contributes only to 17.1% 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 Mekinist.

Family Patents

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Generic Launch

Generic Release Date:

Mekinist's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Mar 02, 2034 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Mekinist Generic API suppliers:

Trametinib Dimethyl Sulfoxide is the generic name for the brand Mekinist. 1 company has already filed for the generic of Mekinist. Check out the entire list of companies who have already received approval for Mekinist's generic





About Mekinist

Mekinist is a drug owned by Novartis Pharmaceuticals Corp. It is used for treating various cancers, including melanoma, anaplastic thyroid cancer, non-small cell lung cancer, and low-grade glioma, in combination with dabrafenib. Mekinist uses Trametinib Dimethyl Sulfoxide as an active ingredient. Mekinist was launched by Novartis in 2013.

Can you believe Mekinist received compensation for the extended wait time during the regulatory approval process?

A supplementary protection certificate (SPC) is a type of intellectual property right granted in the European Union. It provides an extension of the term of protection for a medicinal product that has been authorized for sale in the EU, beyond the 20-year term provided by the basic patent. The aim of SPCs is to compensate for the time taken to get regulatory approval for a new drug, and to provide an incentive for companies to invest in research and development in the field of medicinal products.

Approval Date:

Mekinist was approved by FDA for market use on 29 May, 2013.

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 Mekinist is 29 May, 2013, its NCE-1 date is estimated to be 22 December, 2024.

Active Ingredient:

Mekinist uses Trametinib Dimethyl Sulfoxide as the active ingredient. Check out other Drugs and Companies using Trametinib Dimethyl Sulfoxide ingredient

Treatment:

Mekinist is used for treating various cancers, including melanoma, anaplastic thyroid cancer, non-small cell lung cancer, and low-grade glioma, in combination with dabrafenib.

Dosage:

Mekinist is available in the following dosage forms - solution form for oral use, tablet form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
EQ 0.5MG TABLET Prescription ORAL
EQ 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET Discontinued ORAL
EQ 2MG TABLET Prescription ORAL
EQ 0.05MG BASE/ML SOLUTION Prescription ORAL