Defitelio Patent Expiration

Defitelio is a drug owned by Jazz Pharmaceuticals Inc. It is protected by 3 US drug patents filed from 2021 to 2023 out of which none have expired yet. Defitelio's patents have been open to challenges since 30 March, 2020. Based on its patents and exclusivities, its generic launch date is estimated to be Jun 22, 2032. Details of Defitelio'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).
US11236328 Euglobulin-based method for determining the biological activity of defibrotide
Jun, 2032

(7 years from now)

Active
US11085043 Euglobulin-based method for determining the biological activity of defibrotide
Jun, 2032

(7 years from now)

Active
US11746348 Euglobulin-based method for determining the biological activity of defibrotide
Jun, 2032

(7 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 Defitelio's patents.

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

Activity Date Patent Number
Patent litigations
Recordation of Patent eGrant 05 Sep, 2023 US11746348
Patent Issue Date Used in PTA Calculation 05 Sep, 2023 US11746348
Recordation of Patent Grant Mailed 05 Sep, 2023 US11746348
Mail Patent eGrant Notification 05 Sep, 2023 US11746348
Email Notification 05 Sep, 2023 US11746348
Patent eGrant Notification 05 Sep, 2023 US11746348
Electronic Review 18 Aug, 2023 US11746348
Email Notification 18 Aug, 2023 US11746348
Issue Notification Mailed 16 Aug, 2023 US11746348
Application Is Considered Ready for Issue 27 Jul, 2023 US11746348


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

Exclusivity Information

Defitelio holds 3 exclusivities. All of its exclusivities have expired in 2023. Details of Defitelio's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Mar 30, 2021
Orphan Drug Exclusivity(ODE) Mar 30, 2023
Orphan Drug Exclusivity(ODE-112) Mar 30, 2023

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

Defitelio's Oppositions Filed in EPO

Defitelio has faced multiple oppositions in the European Patent Office. The earliest opposition was filed on Aug 29, 2018, by Aechter, Bernd. This opposition was filed on patent number EP12756826A. Click below to reveal the latest opposition data.


Application Filing Date Opposition Party Legal Status
Patent litigations
EP12756826A Aug, 2018 Aechter, Bernd Patent maintained as amended


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

Defitelio's Family Patents

Defitelio has patent protection in a total of 17 countries. It's US patent count contributes only to 23.1% 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 Defitelio.

Family Patents

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Generic Launch

Generic Release Date:

Defitelio's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Jun 22, 2032 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Defitelio Generics:

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





About Defitelio

Defitelio is a drug owned by Jazz Pharmaceuticals Inc. It is used for treating hepatic veno-occlusive disease following hematopoietic stem cell transplantation in adults and pediatric patients. Defitelio uses Defibrotide Sodium as an active ingredient. Defitelio was launched by Jazz Pharms Inc in 2016.

Approval Date:

Defitelio was approved by FDA for market use on 30 March, 2016.

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 Defitelio is 30 March, 2016, its NCE-1 date is estimated to be 30 March, 2020.

Active Ingredient:

Defitelio uses Defibrotide Sodium as the active ingredient. Check out other Drugs and Companies using Defibrotide Sodium ingredient

Treatment:

Defitelio is used for treating hepatic veno-occlusive disease following hematopoietic stem cell transplantation in adults and pediatric patients.

Dosage:

Defitelio is available in solution form for intravenous use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
200MG/2.5ML (80MG/ML) SOLUTION Prescription INTRAVENOUS