Pharsight

Drug Patents owned by Takeda Pharms Usa

1. List of Actoplus Met drug patents

ACTOPLUS MET's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9101660 TAKEDA PHARMS USA Solid preparation
Jan, 2027

(3 years from now)

US9320714 TAKEDA PHARMS USA Tablet
Feb, 2029

(5 years from now)

Drugs and Companies using METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE ingredient

Market Authorisation Date: 29 August, 2005

Treatment: NA

Dosage: TABLET;ORAL

More Information on Dosage

ACTOPLUS MET family patents

7

Japan

4

United States

2

Portugal

2

Spain

2

Korea, Republic of

2

Canada

2

New Zealand

2

European Union

1

Israel

1

South Africa

1

Denmark

1

Mexico

1

Australia

1

Hong Kong

1

Russia

1

Slovenia

1

Morocco

1

Norway

1

Costa Rica

1

Colombia

1

Brazil

1

Cyprus

1

Poland

1

China

1

Ukraine

2. List of Actoplus Met Xr drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8668931 TAKEDA PHARMS USA Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
Sep, 2023

(5 months from now)

US8470368 TAKEDA PHARMS USA Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
Sep, 2023

(5 months from now)

US9060941 TAKEDA PHARMS USA Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
Sep, 2023

(5 months from now)

US7959946 TAKEDA PHARMS USA Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
Jul, 2026

(3 years from now)

US7785627 TAKEDA PHARMS USA Pharmaceutical formulation containing a biguanide and a thiazolidinedione derivative
Jul, 2026

(3 years from now)

Drugs and Companies using METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE ingredient

Market Authorisation Date: 12 May, 2009

Treatment: NA

Dosage: TABLET, EXTENDED RELEASE;ORAL

How can I launch a generic of ACTOPLUS MET XR before it's patent expiration?
More Information on Dosage

ACTOPLUS MET XR family patents

17

United States

7

Korea, Republic of

6

Japan

5

China

4

Australia

4

European Union

3

Hong Kong

3

Spain

3

Canada

3

New Zealand

2

Brazil

2

Taiwan, Province of China

1

Israel

1

South Africa

1

Mexico

1

Morocco

1

Norway

1

Costa Rica

1

Argentina

1

Singapore

1

Malaysia

1

Peru

1

Georgia

1

Ukraine

EA

1

EA

3. List of Alunbrig drug patents

ALUNBRIG's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US9012462 TAKEDA PHARMS USA Phosphorous derivatives as kinase inhibitors
Apr, 2031

(8 years from now)

US10385078 TAKEDA PHARMS USA Crystalline forms of 5-chloro-N4-[-2-(dimethylphosphoryl)phenyl]-N2-{2-methoxy-4-[4-(4-methylpiperazin-1-YL) piperidin-1-YL]phenyl}pyrimidine-2,4-diamine
Nov, 2035

(12 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9273077 TAKEDA PHARMS USA Phosphorus derivatives as kinase inhibitors
May, 2029

(6 years from now)

US9611283 TAKEDA PHARMS USA Methods for inhibiting cell proliferation in ALK-driven cancers
Apr, 2034

(11 years from now)

Exclusivity Exclusivity Expiration
Orphan Drug Exclusivity (ODE) May 22, 2027
New Indication (I) May 22, 2023

Drugs and Companies using BRIGATINIB ingredient

Market Authorisation Date: 28 April, 2017

Treatment: Treatment of anaplastic lymphoma kinase (alk)-positive metastatic non-small cell lung cancer (nsclc)

Dosage: TABLET;ORAL

More Information on Dosage

ALUNBRIG family patents

22

United States

9

Japan

5

Korea, Republic of

4

Israel

4

China

4

European Union

3

Mexico

3

Lithuania

3

Hungary

2

Denmark

2

Australia

2

Slovenia

2

Norway

2

Croatia

2

Portugal

2

Spain

EA

2

EA

2

Canada

1

South Africa

1

Hong Kong

1

Philippines

1

Costa Rica

1

Singapore

1

Colombia

1

Brazil

1

Cyprus

1

Netherlands

1

Peru

1

Poland

1

Dominican Republic

1

Chile

1

RS

1

Ecuador

1

Luxembourg

1

Ukraine

1

Tunisia

1

New Zealand

4. List of Colcrys drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7964647 TAKEDA PHARMS USA Colchicine compositions and methods
Oct, 2028

(5 years from now)

US8093297 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Oct, 2028

(5 years from now)

US8097655 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics
Oct, 2028

(5 years from now)

US8415396 TAKEDA PHARMS USA Colchine compositions and methods
Oct, 2028

(5 years from now)

US8093296 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics
Oct, 2028

(5 years from now)

US8093298 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics
Oct, 2028

(5 years from now)

US8415395 TAKEDA PHARMS USA Colchicine compositions and methods
Oct, 2028

(5 years from now)

US7981938 TAKEDA PHARMS USA Colchicine compositions and methods
Oct, 2028

(5 years from now)

US7964648 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Oct, 2028

(5 years from now)

US7935731 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics
Dec, 2028

(5 years from now)

US7619004 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics
Dec, 2028

(5 years from now)

US7601758 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and macrolide antibiotics in the treatment of gout flares
Feb, 2029

(5 years from now)

US7820681 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Feb, 2029

(5 years from now)

US7906519 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Feb, 2029

(5 years from now)

US8440721 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Feb, 2029

(5 years from now)

US8440722 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Feb, 2029

(5 years from now)

US7915269 TAKEDA PHARMS USA Methods for concomitant administration of colchicine and a second active agent
Feb, 2029

(5 years from now)

Drugs and Companies using COLCHICINE ingredient

Market Authorisation Date: 29 July, 2009

Treatment: Method of treating gout flares; For the treatment and prophylaxis of gout flares & the treatment of familial mediterranean fever; Method of using colchicine for the prophylaxis of gout flares; Method ...

Dosage: TABLET;ORAL

How can I launch a generic of COLCRYS before it's patent expiration?
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COLCRYS family patents

32

United States

5. List of Dexilant drug patents

DEXILANT's oppositions filed in EPO
Can you believe DEXILANT received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US6664276 TAKEDA PHARMS USA Benzimidazole compound crystal
Jan, 2023

(2 months ago)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6664276

(Pediatric)

 TAKEDA PHARMS USA Benzimidazole compound crystal
Jul, 2023

(3 months from now)

US8722084 TAKEDA PHARMS USA Controlled release preparation
Oct, 2023

(6 months from now)

US8784885 TAKEDA PHARMS USA Controlled release preparation
Oct, 2023

(6 months from now)

US8784885

(Pediatric)

 TAKEDA PHARMS USA Controlled release preparation
Apr, 2024

(1 year, 13 days from now)

US8722084

(Pediatric)

 TAKEDA PHARMS USA Controlled release preparation
Apr, 2024

(1 year, 13 days from now)

US8461187 TAKEDA PHARMS USA Multiple PPI dosage form
Jan, 2026

(2 years from now)

US9238029 TAKEDA PHARMS USA Multiple PPI dosage form
Jan, 2026

(2 years from now)

US9011926 TAKEDA PHARMS USA Method for producing granules
Feb, 2026

(2 years from now)

US8461187

(Pediatric)

 TAKEDA PHARMS USA Multiple PPI dosage form
Jul, 2026

(3 years from now)

US7790755 TAKEDA PHARMS USA Controlled release preparation
Aug, 2026

(3 years from now)

US8105626 TAKEDA PHARMS USA Granules containing acid-unstable chemical in large amount
Sep, 2026

(3 years from now)

US7790755

(Pediatric)

 TAKEDA PHARMS USA Controlled release preparation
Feb, 2027

(3 years from now)

US8105626

(Pediatric)

 TAKEDA PHARMS USA Granules containing acid-unstable chemical in large amount
Mar, 2027

(3 years from now)

US8871273 TAKEDA PHARMS USA Method for producing granules
Jan, 2028

(4 years from now)

US8173158 TAKEDA PHARMS USA Methods of treating gastrointestinal disorders independent of the intake of food
Mar, 2030

(6 years from now)

US8173158

(Pediatric)

 TAKEDA PHARMS USA Methods of treating gastrointestinal disorders independent of the intake of food
Sep, 2030

(7 years from now)

US9233103 TAKEDA PHARMS USA Methods for treating heartburn, gastric bleeding or hemorrhage in patients receiving clopidogrel therapy
Mar, 2032

(8 years from now)

Drugs and Companies using DEXLANSOPRAZOLE ingredient

Market Authorisation Date: 30 January, 2009

Treatment: For the treatment of heartburn associated with symptomatic non-erosive gastroesophageal disease (gerd); To maintain healing of ee and relief of heartburn; For healing of all grades of erosive esophagi...

Dosage: CAPSULE, DELAYED RELEASE;ORAL

How can I launch a generic of DEXILANT before it's patent expiration?
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DEXILANT family patents

35

United States

23

Japan

12

European Union

9

Korea, Republic of

8

Canada

7

Argentina

7

Spain

6

China

5

Denmark

5

Australia

5

Brazil

5

Portugal

5

Cyprus

4

Mexico

4

Hong Kong

4

Malaysia

4

Taiwan, Province of China

3

Israel

3

Russia

3

Norway

3

Costa Rica

3

Peru

3

Poland

3

New Zealand

2

South Africa

2

Slovenia

2

Singapore

OA

1

OA

1

Austria

1

Belgium

1

Hungary

1

Morocco

1

Germany

1

Colombia

1

Chile

6. List of Dexilant Solutab drug patents

DEXILANT SOLUTAB's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US6664276 TAKEDA PHARMS USA Benzimidazole compound crystal
Jan, 2023

(2 months ago)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6664276

(Pediatric)

 TAKEDA PHARMS USA Benzimidazole compound crystal
Jul, 2023

(3 months from now)

US8784885 TAKEDA PHARMS USA Controlled release preparation
Oct, 2023

(6 months from now)

US8784885

(Pediatric)

 TAKEDA PHARMS USA Controlled release preparation
Apr, 2024

(1 year, 13 days from now)

US9238029 TAKEDA PHARMS USA Multiple PPI dosage form
Jan, 2026

(2 years from now)

US8461187 TAKEDA PHARMS USA Multiple PPI dosage form
Jan, 2026

(2 years from now)

US9011926 TAKEDA PHARMS USA Method for producing granules
Feb, 2026

(2 years from now)

US8461187

(Pediatric)

 TAKEDA PHARMS USA Multiple PPI dosage form
Jul, 2026

(3 years from now)

US8871273 TAKEDA PHARMS USA Method for producing granules
Jan, 2028

(4 years from now)

US8871273

(Pediatric)

 TAKEDA PHARMS USA Method for producing granules
Jul, 2028

(5 years from now)

US9241910 TAKEDA PHARMS USA Orally-disintegrating solid preparation
Mar, 2029

(5 years from now)

Drugs and Companies using DEXLANSOPRAZOLE ingredient

Market Authorisation Date: 26 January, 2016

Treatment: Treatment of heartburn associated with non-erosive gastroesophageal reflux disease (gerd) for 4 weeks; Maintain healing of erosive esophagitis (ee) for up to 6 months

Dosage: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE;ORAL

More Information on Dosage

DEXILANT SOLUTAB family patents

30

United States

21

Japan

10

European Union

8

Argentina

7

Korea, Republic of

7

Canada

5

Australia

5

Brazil

5

Spain

5

Peru

5

Taiwan, Province of China

5

China

4

Mexico

4

Costa Rica

4

Malaysia

4

New Zealand

3

South Africa

3

Denmark

3

Hong Kong

3

Norway

3

Portugal

3

Cyprus

3

Poland

2

Israel

2

Slovenia

2

Morocco

2

Chile

OA

1

OA

1

Austria

1

Belgium

1

Hungary

1

Uruguay

1

Germany

1

Colombia

1

Singapore

1

Dominican Republic

1

Ecuador

1

Georgia

1

Ukraine

EA

1

EA

1

Tunisia

7. List of Duetact drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7700128 TAKEDA PHARMS USA Solid preparation comprising an insulin sensitizer, an insulin secretagogue and a polyoxyethylene sorbitan fatty acid ester
Jan, 2027

(3 years from now)

US8071130 TAKEDA PHARMS USA Solid preparation
Jun, 2028

(5 years from now)

Drugs and Companies using GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE ingredient

Market Authorisation Date: 28 July, 2006

Treatment: NA

Dosage: TABLET;ORAL

How can I launch a generic of DUETACT before it's patent expiration?
More Information on Dosage

DUETACT family patents

6

Japan

3

Korea, Republic of

2

South Africa

2

Australia

2

Russia

2

Morocco

2

Norway

2

United States

2

Argentina

2

Croatia

2

Brazil

2

Spain

2

Peru

2

Taiwan, Province of China

2

China

2

Georgia

2

Canada

2

New Zealand

2

European Union

1

Israel

1

Denmark

1

Mexico

1

Jordan

1

Slovenia

1

Hungary

1

Costa Rica

1

Portugal

1

Cyprus

1

Malaysia

1

Poland

1

Ukraine

8. List of Exkivity drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US9796712 TAKEDA PHARMS USA Heteroaryl compounds for kinase inhibition
May, 2035

(12 years from now)

US10227342 TAKEDA PHARMS USA Heteroaryl compounds for kinase inhibition
May, 2035

(12 years from now)

Exclusivity Exclusivity Expiration
New Chemical Entity Exclusivity (NCE) Sep 15, 2026
Orphan Drug Exclusivity (ODE) Sep 15, 2028

Drugs and Companies using MOBOCERTINIB SUCCINATE ingredient

NCE-1 date: 2025-09-15

Market Authorisation Date: 15 September, 2021

Treatment: Treatment of patients with non-small cell lung cancer (nsclc) with epidermal growth factor receptor (egfr) exon 20 exon insertion mutations whose disease has progressed on or after platinum-based chem...

Dosage: CAPSULE;ORAL

More Information on Dosage

EXKIVITY family patents

6

United States

4

Japan

3

European Union

2

Israel

2

Australia

2

Morocco

2

Singapore

2

Korea, Republic of

2

Chile

2

China

2

Georgia

2

New Zealand

1

South Africa

1

Denmark

1

Turkey

1

Mexico

1

Saudi Arabia

1

Slovenia

1

Lithuania

1

Hungary

1

Philippines

1

Costa Rica

1

Cuba

1

Colombia

1

Brazil

1

Croatia

1

Portugal

1

Cyprus

1

Spain

1

Peru

1

Poland

1

RS

1

Ecuador

1

Ukraine

EA

1

EA

1

Canada

1

Tunisia

1

ME

9. List of Fosrenol drug patents

FOSRENOL's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7381428 TAKEDA PHARMS USA Stabilized lanthanum carbonate compositions
Aug, 2024

(1 year, 4 months from now)

US7465465 TAKEDA PHARMS USA Pharmaceutical formulation comprising lanthanum compounds
Aug, 2024

(1 year, 4 months from now)

US9023397 TAKEDA PHARMS USA Capsule and powder formulations containing lanthanum compounds
Dec, 2030

(7 years from now)

US8980327 TAKEDA PHARMS USA Capsule and powder formulations containing lanthanum compounds
Dec, 2030

(7 years from now)

Drugs and Companies using LANTHANUM CARBONATE ingredient

Market Authorisation Date: 26 October, 2004

Treatment: Reduction of serum phosphate in patients with end stage renal disease

Dosage: TABLET, CHEWABLE;ORAL

How can I launch a generic of FOSRENOL before it's patent expiration?
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FOSRENOL family patents

14

United States

7

Japan

6

European Union

5

Denmark

4

Australia

4

Slovenia

4

Portugal

4

Cyprus

4

Spain

4

Poland

4

China

4

Canada

3

Brazil

3

Korea, Republic of

EA

3

EA

2

South Africa

2

Austria

2

Hungary

2

Norway

2

Germany

1

Israel

IB

1

IB

1

Mexico

1

Finland

1

Hong Kong

1

Argentina

1

Singapore

1

Peru

1

Czech Republic

1

Iceland

1

Taiwan, Province of China

1

New Zealand

10. List of Iclusig drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US8114874 TAKEDA PHARMS USA Substituted acetylenic imidazo[1,2-B]pyridazine compounds as kinase inhibitors
Jan, 2027

(3 years from now)

US11384086 TAKEDA PHARMS USA Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1- yl)methyl]-3-(trifluoromethyl)phenyl}benzamide and its mono hydrochloride salt
Dec, 2033

(10 years from now)

US11192897 TAKEDA PHARMS USA Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide and its mono hydrochloride salt
Dec, 2033

(10 years from now)

US9493470 TAKEDA PHARMS USA Crystalline forms of 3-(imidazo[1,2-B] pyridazin-3-ylethynyl)-4-methyl-N-{4-[(4-methylpiperazin-1-yl) methyl]-3-(trifluoromethyl)phenyl}benzamide and its mono hydrochloride salt
Dec, 2033

(10 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9029533 TAKEDA PHARMS USA Substituted acetylenic imidazo[1,2-A]pyridazines as kinase inhibitors
Dec, 2026

(3 years from now)

US11192895 TAKEDA PHARMS USA Crystalline forms of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide and its mono hydrochloride salt
Dec, 2033

(10 years from now)

Exclusivity Exclusivity Expiration
New Indication (I) Dec 18, 2023

Drugs and Companies using PONATINIB HYDROCHLORIDE ingredient

Market Authorisation Date: 14 December, 2012

Treatment: A method of treating chronic myelogenous leukemia; A method for treating philadelphia chromosome positive acute lymphoblastic leukemia; A method for treating leukemia resulting from a mutation in the ...

Dosage: TABLET;ORAL

How can I launch a generic of ICLUSIG before it's patent expiration?
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ICLUSIG family patents

40

United States

8

Australia

8

China

8

Japan

6

Canada

6

European Union

5

Mexico

4

Israel

EA

4

EA

3

Brazil

3

Spain

3

Korea, Republic of

2

Denmark

2

Slovenia

2

Hungary

2

Portugal

2

Poland

1

Hong Kong

1

Lithuania

1

Cyprus

1

Chile

1

Luxembourg

1

New Zealand

11. List of Intuniv drug patents

Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6811794 TAKEDA PHARMS USA Sustained release pharmaceutical dosage forms with minimized pH dependent dissolution profiles
Jul, 2022

(8 months ago)

US6811794

(Pediatric)

 TAKEDA PHARMS USA Sustained release pharmaceutical dosage forms with minimized pH dependent dissolution profiles
Jan, 2023

(2 months ago)

Drugs and Companies using GUANFACINE HYDROCHLORIDE ingredient

Market Authorisation Date: 02 September, 2009

Treatment: Treatment of attention-deficit hyperactivity disorder

Dosage: TABLET, EXTENDED RELEASE;ORAL

How can I launch a generic of INTUNIV before it's patent expiration?
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INTUNIV family patents

1

United States

12. List of Kazano drug patents

Can you believe KAZANO received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US8288539 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Jun, 2025

(2 years from now)

US7807689 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Jun, 2028

(5 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8173663 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Mar, 2025

(1 year, 11 months from now)

US8900638 TAKEDA PHARMS USA Solid preparation comprising alogliptin and metformin hydrochloride
May, 2029

(6 years from now)

Drugs and Companies using ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE ingredient

Market Authorisation Date: 25 January, 2013

Treatment: Method of treating diabetes comprising administering a compound such as alogliptin; Method of treating diabetes comprising administering alogliptin

Dosage: TABLET;ORAL

How can I launch a generic of KAZANO before it's patent expiration?
More Information on Dosage

KAZANO family patents

12

United States

9

China

7

Japan

3

Israel

3

Argentina

3

Korea, Republic of

3

Taiwan, Province of China

2

South Africa

2

Australia

2

Morocco

2

Norway

2

Costa Rica

2

Brazil

2

Malaysia

2

Spain

2

Peru

2

Georgia

2

Ukraine

EA

2

EA

2

Canada

2

New Zealand

2

European Union

1

Denmark

1

Austria

1

Mexico

1

Jordan

1

Hong Kong

1

Slovenia

1

Hungary

1

Germany

1

Colombia

1

Croatia

1

Portugal

1

Cyprus

1

Netherlands

1

Dominican Republic

1

Poland

1

RS

1

Luxembourg

1

Ecuador

1

Tunisia

13. List of Mydayis drug patents

MYDAYIS Litigations
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6913768 TAKEDA PHARMS USA Sustained release delivery of amphetamine salts
May, 2023

(a month from now)

US9173857 TAKEDA PHARMS USA Controlled dose drug delivery system
May, 2026

(3 years from now)

US8846100 TAKEDA PHARMS USA Controlled dose drug delivery system
Aug, 2029

(6 years from now)

Exclusivity Exclusivity Expiration
Pediatric Exclusivity (PED) Mar 13, 2023

Drugs and Companies using AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE ingredient

Market Authorisation Date: 20 June, 2017

Treatment: Treatment of attention deficit hyperactivity disorder

Dosage: CAPSULE, EXTENDED RELEASE;ORAL

How can I launch a generic of MYDAYIS before it's patent expiration?
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MYDAYIS family patents

9

United States

1

Israel

1

South Africa

OA

1

OA

1

Denmark

1

Austria

1

Mexico

1

Australia

1

Hong Kong

1

Slovenia

1

Morocco

1

Norway

1

Costa Rica

AP

1

AP

1

Germany

1

Croatia

1

Brazil

1

Cyprus

1

Spain

1

Korea, Republic of

1

Poland

1

Iceland

1

China

1

Ecuador

1

Ukraine

1

Japan

EA

1

EA

1

Canada

1

New Zealand

1

European Union

14. List of Nesina drug patents

Can you believe NESINA received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US8288539 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Mar, 2025

(1 year, 11 months from now)

US7807689 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Jun, 2028

(5 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8173663 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Dec, 2025

(2 years from now)

US8697125 TAKEDA PHARMS USA Tablet preparation without causing a tableting trouble
Jun, 2029

(6 years from now)

Drugs and Companies using ALOGLIPTIN BENZOATE ingredient

Market Authorisation Date: 25 January, 2013

Treatment: Method of treating diabetes comprising administering a compound such as alogliptin; Method of treating diabetes comprising administering alogliptin

Dosage: TABLET;ORAL

How can I launch a generic of NESINA before it's patent expiration?
More Information on Dosage

NESINA family patents

12

United States

8

China

6

Japan

3

Argentina

3

Taiwan, Province of China

2

Israel

2

Norway

2

Croatia

2

Spain

2

Korea, Republic of

2

Canada

2

European Union

1

South Africa

1

Denmark

1

Austria

1

Mexico

1

Australia

1

Hong Kong

1

Slovenia

1

Morocco

1

Hungary

1

Costa Rica

1

Germany

1

Brazil

1

Portugal

1

Cyprus

1

Malaysia

1

Netherlands

1

Peru

1

Poland

1

Chile

1

RS

1

Luxembourg

1

Georgia

1

Ukraine

EA

1

EA

1

New Zealand

15. List of Ninlaro drug patents

NINLARO's oppositions filed in EPO
Can you believe NINLARO received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US8546608 TAKEDA PHARMS USA Proteasome inhibitors and methods of using the same
Aug, 2024

(1 year, 4 months from now)

US7687662 TAKEDA PHARMS USA Proteasome inhibitors
Aug, 2027

(4 years from now)

US8530694 TAKEDA PHARMS USA Proteasome inhibitors
Aug, 2027

(4 years from now)

US8003819 TAKEDA PHARMS USA Proteasome inhibitors
Aug, 2027

(4 years from now)

US8859504 TAKEDA PHARMS USA Boronate ester compounds and pharmaceutical compositions thereof
Jun, 2029

(6 years from now)

US7442830 TAKEDA PHARMS USA Proteasome inhibitors
Nov, 2029

(6 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9233115 TAKEDA PHARMS USA Proteasome inhibitors and methods of using the same
Aug, 2024

(1 year, 4 months from now)

US8871745 TAKEDA PHARMS USA Proteasome inhibitors
Aug, 2027

(4 years from now)

US9175017 TAKEDA PHARMS USA Boronate ester compounds and pharmaceutical compositions thereof
Jun, 2029

(6 years from now)

Exclusivity Exclusivity Expiration
Orphan Drug Exclusivity (ODE) Nov 20, 2022

Drugs and Companies using IXAZOMIB CITRATE ingredient

Market Authorisation Date: 20 November, 2015

Treatment: Use in combination with lenalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received at least one prior therapy

Dosage: CAPSULE;ORAL

How can I launch a generic of NINLARO before it's patent expiration?
More Information on Dosage

NINLARO family patents

47

United States

15

China

12

Hong Kong

12

Korea, Republic of

10

Japan

10

European Union

9

Israel

8

Taiwan, Province of China

7

Argentina

7

New Zealand

6

South Africa

6

Brazil

6

Peru

EA

6

EA

5

Mexico

4

Denmark

4

Philippines

4

Portugal

4

Malaysia

4

Spain

4

Ukraine

4

Canada

3

Australia

3

Slovenia

3

Norway

3

Costa Rica

3

Singapore

3

Croatia

3

Cyprus

3

Poland

3

Ecuador

3

Georgia

2

Chile

2

RS

1

Austria

1

Lithuania

1

Hungary

1

Morocco

1

Germany

1

Colombia

1

Netherlands

1

Dominican Republic

1

Iceland

1

Luxembourg

1

Tunisia

16. List of Omontys drug patents

Can you believe OMONTYS received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US7919118 TAKEDA PHARMS USA Spacer moiety for poly (ethylene glycol) modified peptide based compounds
May, 2024

(1 year, 1 month from now)

US7084245 TAKEDA PHARMS USA Peptides that bind to the erythropoietin receptor
May, 2024

(1 year, 1 month from now)

US7528104 TAKEDA PHARMS USA Peptides that bind to the erythropoietin receptor
May, 2024

(1 year, 1 month from now)

US7414105 TAKEDA PHARMS USA Peptides that bind to the erythropoietin receptor
May, 2024

(1 year, 1 month from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7919461 TAKEDA PHARMS USA Erythropoietin receptor peptide formulations and uses
Jun, 2026

(3 years from now)

US7550433 TAKEDA PHARMS USA Erythropoietin receptor peptide formulations and uses
Jun, 2026

(3 years from now)

Drugs and Companies using PEGINESATIDE ACETATE ingredient

Market Authorisation Date: 27 March, 2012

Treatment: Treatment of anemia due to chronic kidney disease

Dosage: SOLUTION;INTRAVENOUS, SUBCUTANEOUS

More Information on Dosage

OMONTYS family patents

32

United States

9

Japan

6

Korea, Republic of

6

European Union

5

New Zealand

4

South Africa

4

Mexico

4

Australia

4

Norway

4

Brazil

4

China

EA

4

EA

4

Canada

3

Iceland

2

Denmark

2

Hong Kong

2

Slovenia

2

Costa Rica

2

Singapore

2

Croatia

2

Portugal

2

Cyprus

2

Spain

2

Poland

2

Ukraine

1

Israel

OA

1

OA

1

Austria

1

Morocco

AP

1

AP

1

Germany

YU

1

Yugoslavia

1

Georgia

1

ME

17. List of Oseni drug patents

Can you believe OSENI received compensation for the extended wait time during the regulatory approval process?
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US8288539 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Mar, 2025

(1 year, 11 months from now)

US7807689 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Jun, 2028

(5 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8173663 TAKEDA PHARMS USA Dipeptidyl peptidase inhibitors
Mar, 2025

(1 year, 11 months from now)

US8637079 TAKEDA PHARMS USA Solid preparation comprising alogliptin and pioglitazone
Jun, 2029

(6 years from now)

Drugs and Companies using ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE ingredient

Market Authorisation Date: 25 January, 2013

Treatment: Method of treating diabetes comprising administering a compound such as alogliptin; Method of treating diabetes comprising administering alogliptin

Dosage: TABLET;ORAL

More Information on Dosage

OSENI family patents

12

United States

9

China

6

Japan

4

Taiwan, Province of China

3

Israel

3

Argentina

3

Korea, Republic of

2

South Africa

2

Denmark

2

Austria

2

Mexico

2

Australia

2

Hong Kong

2

Slovenia

2

Morocco

2

Norway

2

Costa Rica

2

Germany

2

Brazil

2

Croatia

2

Portugal

2

Cyprus

2

Malaysia

2

Spain

2

Poland

2

RS

2

Georgia

2

Ukraine

EA

2

EA

2

Canada

2

New Zealand

2

European Union

1

Jordan

1

Hungary

1

Netherlands

1

Dominican Republic

1

Peru

1

Chile

1

Ecuador

1

Luxembourg

1

Tunisia

1

ME

18. List of Trintellix drug patents

TRINTELLIX's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US7144884 TAKEDA PHARMS USA Phenyl-piperazine derivatives as serotonin reuptake inhibitors
Jun, 2026

(3 years from now)

US8722684 TAKEDA PHARMS USA 1-[2-(2,4-dimethylphenylsulfanyl)-phenyl] piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2031

(8 years from now)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8476279 TAKEDA PHARMS USA Phenyl-piperazine derivatives as serotonin reuptake inhibitors
Oct, 2022

(5 months ago)

US9125910 TAKEDA PHARMS USA 1-[2-(2,4 dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US9861630 TAKEDA PHARMS USA 1-[2-(2,4-dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US9125909 TAKEDA PHARMS USA 1-[2-(2,4 dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US9125908 TAKEDA PHARMS USA 1-[2-(2,4-dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US11458134 TAKEDA PHARMS USA 1-[2-(2,4-dimeihylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US9227946 TAKEDA PHARMS USA 1-[2-(2,4 dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1a activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US8969355 TAKEDA PHARMS USA 1-[2-(2,4 dimethylphenylsulfanyl)-phenyl]piperazine as a compound with combined serotonin reuptake, 5-HT3 and 5-HT1a activity for the treatment of cognitive impairment
Jun, 2027

(4 years from now)

US9278096 TAKEDA PHARMS USA Therapeutic uses of compounds having combined SERT, 5-HT3 and 5-HT1A activity
Mar, 2032

(8 years from now)

Exclusivity Exclusivity Expiration
M (M) Jan 22, 2024

Drugs and Companies using VORTIOXETINE HYDROBROMIDE ingredient

Market Authorisation Date: 30 September, 2013

Treatment: Method of treating an affective disorder such as depression; Use in the treatment of major depressive disorder to improve processing speed, an aspect of cognitive function; Method of treating depressi...

Dosage: TABLET;ORAL

How can I launch a generic of TRINTELLIX before it's patent expiration?
More Information on Dosage

TRINTELLIX family patents

28

United States

12

Denmark

11

Japan

8

Brazil

7

Korea, Republic of

6

China

5

Spain

5

European Union

4

Austria

4

Australia

4

Hong Kong

4

Norway

4

Argentina

4

Portugal

4

Cyprus

4

Poland

4

Ukraine

EA

4

EA

3

Mexico

3

Slovenia

3

Hungary

3

Germany

3

Croatia

3

Malaysia

3

RS

3

Canada

3

New Zealand

2

Israel

2

South Africa

2

Colombia

2

Iceland

2

Chile

2

Taiwan, Province of China

1

Egypt

1

Lithuania

1

Belgium

1

Morocco

YU

1

Yugoslavia

1

Netherlands

1

Luxembourg

1

Tunisia

1

ME

19. List of Uloric drug patents

ULORIC's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7361676 TAKEDA PHARMS USA Solid preparation containing single crystal form
Mar, 2024

(11 months from now)

US8372872 TAKEDA PHARMS USA Methods for concomitant treatment of theophylline and febuxostat
Sep, 2031

(8 years from now)

US9107912 TAKEDA PHARMS USA Methods for concomitant treatment of theophylline and febuxostat
Sep, 2031

(8 years from now)

Drugs and Companies using FEBUXOSTAT ingredient

Market Authorisation Date: 13 February, 2009

Treatment: Use of febuxostat for the management of hyperuricemia in patients suffering from gout and, when used with theophylline without the need for dose adjustment of theophylline

Dosage: TABLET;ORAL

How can I launch a generic of ULORIC before it's patent expiration?
More Information on Dosage

ULORIC family patents

6

United States

4

Japan

3

China

2

Canada

2

Spain

2

Australia

2

Korea, Republic of

2

European Union

1

Hong Kong

1

Slovenia

1

Russia

1

Brazil

1

Portugal

1

Denmark

1

Cyprus

20. List of Velcade drug patents

VELCADE's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US6713446 TAKEDA PHARMS USA Formulation of boronic acid compounds
Jan, 2022

(1 year, 2 months ago)

US6958319 TAKEDA PHARMS USA Formulation of boronic acid compounds
Jan, 2022

(1 year, 2 months ago)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6713446

(Pediatric)

 TAKEDA PHARMS USA Formulation of boronic acid compounds
Jul, 2022

(8 months ago)

US6958319

(Pediatric)

 TAKEDA PHARMS USA Formulation of boronic acid compounds
Jul, 2022

(8 months ago)

Exclusivity Exclusivity Expiration
Pediatric Exclusivity (PED) Apr 8, 2022

Drugs and Companies using BORTEZOMIB ingredient

Market Authorisation Date: 13 May, 2003

Treatment: NA

Dosage: INJECTABLE;INTRAVENOUS, SUBCUTANEOUS

How can I launch a generic of VELCADE before it's patent expiration?
More Information on Dosage

VELCADE family patents

9

United States

4

European Union

3

Denmark

3

Cyprus

3

Spain

2

Japan

2

Portugal

2

Canada

1

Germany

1

Hong Kong

1

Turkey

1

Australia

1

Austria

21. List of Vyvanse drug patents

VYVANSE's oppositions filed in EPO
Patent Number Company Patent Title Patent Expiry Activity Alert
These patents protects the active chemical substance. Only patent owner can launch products that use this active substance.
US7659253 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7662787 TAKEDA PHARMS USA Abuse resistant lysine amphetamine compounds
Feb, 2023

(a month ago)

US7655630 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7671031 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7659254 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7105486 TAKEDA PHARMS USA Abuse-resistant amphetamine compounds
Feb, 2023

(a month ago)

US7662788 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7674774 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7678771 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7723305 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7713936 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7700561 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7687466 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7223735 TAKEDA PHARMS USA Abuse resistant lysine amphetamine compounds
Feb, 2023

(a month ago)

US7718619 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7678770 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7687467 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7671030 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Feb, 2023

(a month ago)

US7105486

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine compounds
Aug, 2023

(4 months from now)

US7718619

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7223735

(Pediatric)

 TAKEDA PHARMS USA Abuse resistant lysine amphetamine compounds
Aug, 2023

(4 months from now)

US7655630

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7659253

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7662788

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7662787

(Pediatric)

 TAKEDA PHARMS USA Abuse resistant lysine amphetamine compounds
Aug, 2023

(4 months from now)

US7659254

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7671030

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7671031

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7674774

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7678770

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7678771

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7687466

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7687467

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7713936

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7700561

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

US7723305

(Pediatric)

 TAKEDA PHARMS USA Abuse-resistant amphetamine prodrugs
Aug, 2023

(4 months from now)

Drugs and Companies using LISDEXAMFETAMINE DIMESYLATE ingredient

Market Authorisation Date: 28 January, 2017

Treatment: For the treatment of attention deficit hyperactivity disorder (adhd); Treatment of attention deficit hyperactivity disorder (adhd) in adults; Indicated for the treatment of attention-deficit/hyperacti...

Dosage: TABLET, CHEWABLE;ORAL

How can I launch a generic of VYVANSE before it's patent expiration?
More Information on Dosage

VYVANSE family patents

688

United States

18

Australia

15

European Union

13

Japan

11

Canada

9

Korea, Republic of

8

China

5

Austria

4

Israel

4

Spain

3

Mexico

3

Brazil

2

South Africa

2

Norway

2

Germany

EA

2

EA

2

New Zealand

1

Denmark

1

Egypt

1

Hong Kong

1

Slovenia

1

Russia

1

Singapore

1

Portugal

1

Cyprus

1

Netherlands

1

Poland

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