Imbruvica Patent Expiration

Imbruvica is a drug owned by Pharmacyclics Llc. It is protected by 81 US drug patents filed from 2017 to 2024 out of which none have expired yet. Imbruvica's patents will be open to challenges from 24 February, 2025. Based on its patents and exclusivities, its generic launch date is estimated to be Sep 03, 2036. Details of Imbruvica'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.
US9296753 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Oct, 2033

(8 years from now)

Active
US9725455 Crystalline forms of a bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10106548 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10125140 Crystalline forms of a bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US8008309 Inhibitors of bruton's tyrosine kinase
Nov, 2027

(2 years from now)

Active
US8735403 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US9181257 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8957079 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US7514444 Inhibitors of bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8697711 Inhibitors of bruton'S tyrosine kinase
Dec, 2026

(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).
US10828259

(Pediatric)

Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Sep, 2036

(11 years from now)

Active
US10010507

(Pediatric)

Pharmaceutical formulations of a bruton's tyrosine kinase inhibitor
Sep, 2036

(11 years from now)

Active
US10213386

(Pediatric)

Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Sep, 2036

(11 years from now)

Active
US9655857

(Pediatric)

Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Sep, 2036

(11 years from now)

Active
US9655857 Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Mar, 2036

(11 years from now)

Active
US10213386 Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Mar, 2036

(11 years from now)

Active
US10010507 Pharmaceutical formulations of a bruton's tyrosine kinase inhibitor
Mar, 2036

(11 years from now)

Active
US10828259 Pharmaceutical formulations of a Bruton's tyrosine kinase inhibitor
Mar, 2036

(11 years from now)

Active
US9795604

(Pediatric)

Methods of treating and preventing graft versus host disease
Apr, 2035

(10 years from now)

Active
US10695350

(Pediatric)

Methods of treating and preventing graft versus host disease
Apr, 2035

(10 years from now)

Active
US10463668

(Pediatric)

Methods of treating and preventing graft versus host disease
Apr, 2035

(10 years from now)

Active
US10463668 Methods of treating and preventing graft versus host disease
Oct, 2034

(9 years from now)

Active
US9795604 Methods of treating and preventing graft versus host disease
Oct, 2034

(9 years from now)

Active
US10695350 Methods of treating and preventing graft versus host disease
Oct, 2034

(9 years from now)

Active
US9296753

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Apr, 2034

(9 years from now)

Active
US9540382

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Feb, 2034

(9 years from now)

Active
US10106548

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US10125140

(Pediatric)

Crystalline forms of a bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US10961251

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US9725455

(Pediatric)

Crystalline forms of a bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US10752634

(Pediatric)

Crystalline forms of a brutons tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US10294232

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US10294231

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US9713617

(Pediatric)

Crystalline forms of a Bruton's tyrosine kinase inhibitor
Dec, 2033

(9 years from now)

Active
US9540382 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Aug, 2033

(8 years from now)

Active
US10752634 Crystalline forms of a brutons tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US9713617 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10961251 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10294231 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10294232 Crystalline forms of a Bruton's tyrosine kinase inhibitor
Jun, 2033

(8 years from now)

Active
US10478439

(Pediatric)

Use of inhibitors of bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US9814721

(Pediatric)

Use of inhibitors of bruton'S tyrosine kinase (BTK)
Dec, 2031

(7 years from now)

Active
US10653696

(Pediatric)

Use of inhibitors of bruton's tyrosine kinase (BTK)
Dec, 2031

(7 years from now)

Active
US8754090

(Pediatric)

Use of inhibitors of bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US9125889

(Pediatric)

Use of inhibitors of Bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US10004746

(Pediatric)

Use of inhibitors of Bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US9801883

(Pediatric)

Use of inhibitors of bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US9801881

(Pediatric)

Use of inhibitors of bruton's tyrosine kinase (BTK)
Dec, 2031

(7 years from now)

Active
US8999999

(Pediatric)

Use of inhibitors of Bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US10016435

(Pediatric)

Use of inhibitors of Bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US10751342

(Pediatric)

Use of inhibitors of Bruton's tyrosine kinase (Btk)
Dec, 2031

(7 years from now)

Active
US9801881 Use of inhibitors of bruton's tyrosine kinase (BTK)
Jun, 2031

(6 years from now)

Active
US10016435 Use of inhibitors of Bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US8999999 Use of inhibitors of Bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US10004746 Use of inhibitors of Bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US9814721 Use of inhibitors of bruton'S tyrosine kinase (BTK)
Jun, 2031

(6 years from now)

Active
US10653696 Use of inhibitors of bruton's tyrosine kinase (BTK)
Jun, 2031

(6 years from now)

Active
US10478439 Use of inhibitors of bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US11672803 Use of inhibitors of Brutons tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US8754090 Use of inhibitors of bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US9125889 Use of inhibitors of Bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US9801883 Use of inhibitors of bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US10751342 Use of inhibitors of Bruton's tyrosine kinase (Btk)
Jun, 2031

(6 years from now)

Active
US8008309

(Pediatric)

Inhibitors of bruton's tyrosine kinase
May, 2028

(3 years from now)

Active
US8563563

(Pediatric)

Inhibitors of bruton's tyrosine kinase
Oct, 2027

(2 years from now)

Active
US8735403

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US7514444

(Pediatric)

Inhibitors of bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8703780

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8957079

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US9181257

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8754091

(Pediatric)

Inhibitors of bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8952015

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8497277

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8476284

(Pediatric)

Inhibitors of Bruton's tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8697711

(Pediatric)

Inhibitors of bruton'S tyrosine kinase
Jun, 2027

(2 years from now)

Active
US8563563 Inhibitors of bruton's tyrosine kinase
Apr, 2027

(2 years from now)

Active
US8703780 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8952015 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8497277 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8476284 Inhibitors of Bruton's tyrosine kinase
Dec, 2026

(2 years from now)

Active
US8754091 Inhibitors of bruton's tyrosine kinase
Dec, 2026

(2 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 Imbruvica's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 8th Year, Large Entity 13 Jun, 2024 US9540382
Request for Trial Granted 01 May, 2024 US11672803 (Litigated)
Payment of Maintenance Fee, 4th Year, Large Entity 11 Apr, 2024 US10828259
Payment of Maintenance Fee, 4th Year, Large Entity 11 Jan, 2024 US10752634
Payment of Maintenance Fee, 4th Year, Large Entity 11 Jan, 2024 US10751342 (Litigated)
Letter from FDA or Dept of Agriculture re PTE application 18 Dec, 2023 US8008309
Payment of Maintenance Fee, 4th Year, Large Entity 10 Nov, 2023 US10695350
Petition Requesting Trial 06 Nov, 2023 US11672803 (Litigated)
Payment of Maintenance Fee, 4th Year, Large Entity 12 Oct, 2023 US10653696 (Litigated)
Payment of Maintenance Fee, 8th Year, Large Entity 10 Aug, 2023 US9296753


While patent expiration is one way of estimating the generic date of a drug, if a patent gets invalidated somehow, the generic of the drug may arrive early. Being aware of all relevant patents can help in avoiding legal pitfalls. Given below are details of the litigation history of Imbruvica and ongoing litigations to help you estimate the early arrival of Imbruvica generic.

Imbruvica's Litigations

Imbruvica been subject to various legal proceedings, including patent litigations. The earliest legal proceeding was initiated on Apr 20, 2015, against patent number US8754090. The petitioner Coalition for Affordable Drugs IV LLC, challenged the validity of this patent, with Pharmacyclics, Inc. as the respondent. Click below to track the latest information on how companies are challenging Imbruvica's patents.

Last updated on November 19, 2024
Patent Proceeding Filing Date Status Respondent Petitioner
Patent litigations
US11672803 November, 2023 Trial Instituted
(01 May, 2024)
Pharmacyclics LLC BeiGene USA, Inc. et al.
US9795604 March, 2019 Final Written Decision
(24 Sep, 2020)
Pharmacyclics LLC et al. Sandoz Inc. et al.
US8754090 April, 2015 Terminated-Denied
(19 Oct, 2015)
Pharmacyclics, Inc. Coalition for Affordable Drugs IV LLC


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

Exclusivity Information

Imbruvica holds 27 exclusivities out of which 22 have expired. Its last outstanding exclusivity is set to expire in 2029. Details of Imbruvica's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Indication(I-680) Feb 12, 2017
New Indication(I-689) Jul 28, 2017
New Indication(I-702) Jan 29, 2018
New Chemical Entity Exclusivity(NCE) Nov 13, 2018
New Indication(I-729) Mar 04, 2019
New Dosing Schedule(D-165) May 06, 2019
New Indication(I-736) May 06, 2019
New Indication(I-737) May 06, 2019
New Indication(I-741) Jan 18, 2020
New Indication(I-753) Aug 02, 2020
Orphan Drug Exclusivity(ODE-55) Nov 13, 2020
Orphan Drug Exclusivity(ODE-60) Feb 12, 2021
Orphan Drug Exclusivity(ODE-72) Jul 28, 2021
New Dosing Schedule(D-176) Aug 24, 2021
M(M-236) Jan 25, 2022
Orphan Drug Exclusivity(ODE-86) Jan 29, 2022
Orphan Drug Exclusivity(ODE-109) Mar 04, 2023
Orphan Drug Exclusivity(ODE-117) May 06, 2023
Orphan Drug Exclusivity(ODE-128) Jan 18, 2024
Orphan Drug Exclusivity(ODE) Aug 02, 2024
ODE*(ODE*) Aug 02, 2024
Orphan Drug Exclusivity(ODE-152) Aug 02, 2024
M(M-14) Aug 24, 2025
New Product(NP) Aug 24, 2025
New Patient Population(NPP) Aug 24, 2025
Pediatric Exclusivity(PED) Feb 24, 2026
Orphan Drug Exclusivity(ODE-405) Aug 24, 2029

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

Imbruvica's Oppositions Filed in EPO

Imbruvica has faced multiple oppositions in the European Patent Office. The earliest opposition was filed on Oct 17, 2018, by Generics (U.K.) Limited. This opposition was filed on patent number EP12166302A. Click below to reveal the latest opposition data.


Application Filing Date Opposition Party Legal Status
Patent litigations
EP12166302A Oct, 2018 Generics (U.K.) Limited Revoked


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

Imbruvica's Family Patents

Imbruvica has patent protection in a total of 43 countries. It's US patent count contributes only to 35.1% 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 Imbruvica.

Family Patents

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Generic Launch

Generic Release Date:

Imbruvica's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Sep 03, 2036 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Imbruvica Generic API suppliers:

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

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

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

Strength Submission Date ANDA(s) Filed First applicant approval Last patent expiry 180 day status
70 mg 14 Dec, 2018 1 31 Mar, 2021 30 Oct, 2033 Eligible
140 mg 13 Nov, 2017 8 31 Mar, 2021 24 Oct, 2034 Deferred
140 mg and 560 mg 05 Nov, 2018 1 03 Mar, 2036
280 mg and 420 mg 14 Dec, 2018 1 03 Mar, 2036





About Imbruvica

Imbruvica is a drug owned by Pharmacyclics Llc. It is used for treating various types of leukemias, lymphomas, and graft-versus-host disease, including those with specific genetic deletions. Imbruvica uses Ibrutinib as an active ingredient. Imbruvica was launched by Pharmacyclics Llc in 2018.

Approval Date:

Imbruvica was approved by FDA for market use on 16 February, 2018.

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 Imbruvica is 16 February, 2018, its NCE-1 date is estimated to be 24 February, 2025.

Active Ingredient:

Imbruvica uses Ibrutinib as the active ingredient. Check out other Drugs and Companies using Ibrutinib ingredient

Treatment:

Imbruvica is used for treating various types of leukemias, lymphomas, and graft-versus-host disease, including those with specific genetic deletions.

Dosage:

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

Strength Dosage Form Availability Application Pathway
280MG TABLET Prescription ORAL
420MG TABLET Prescription ORAL
560MG TABLET Discontinued ORAL
140MG TABLET Prescription ORAL
70MG/ML SUSPENSION Prescription ORAL
70MG CAPSULE Prescription ORAL


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