Pharsight

Ucb Inc patents expiration

1. Briviact patents expiration

BRIVIACT Litigations
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US6784197 UCB INC 2-oxo-1-pyrrolidine derivatives, processes for preparing them and their uses
Feb, 2021

(3 years ago)

US6911461 UCB INC 2-oxo-1-pyrrolidine derivatives, processes for preparing them and their uses
Feb, 2026

(1 year, 10 months from now)

These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8492416 UCB INC 2-oxo-1-pyrrolidine derivatives, processes for preparing them and their uses
Feb, 2021

(3 years ago)

US10729653 UCB INC Pharmaceutical compositions comprising 2-oxo-1-pyrrolidine derivatives
Apr, 2030

(5 years from now)

Drug Exclusivity Drug Exclusivity Expiration
New Patient Population(NPP) Aug 27, 2024
New Chemical Entity Exclusivity(NCE) May 12, 2021

Drugs and Companies using BRIVARACETAM ingredient

NCE-1 date: 12 May, 2020

Market Authorisation Date: 12 May, 2016

Treatment: Treatment of partial-onset seizures in patients 4 years of age and older

Dosage: TABLET;ORAL; SOLUTION;ORAL; SOLUTION;INTRAVENOUS

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

BRIVIACT family patents

Family Patents

2. Fintepla patents expiration

FINTEPLA's oppositions filed in EPO
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US10947183 UCB INC Fenfluramine compositions and methods of preparing the same
Dec, 2036

(12 years from now)

These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US9603814 UCB INC Method for the treatment of Dravet syndrome
May, 2033

(9 years from now)

US10478441 UCB INC Method for the treatment of Dravet syndrome
May, 2033

(9 years from now)

US9603815 UCB INC Method for the treatment of Dravet syndrome
May, 2033

(9 years from now)

US9549909 UCB INC Method for the treatment of dravet syndrome
May, 2033

(9 years from now)

US9610260 UCB INC Method for the treatment of Dravet Syndrome
May, 2033

(9 years from now)

US10478442 UCB INC Method for the treatment of Dravet Syndrome
May, 2033

(9 years from now)

US9610260

(Pediatric)

UCB INC Method for the treatment of Dravet Syndrome
Nov, 2033

(9 years from now)

US9603815

(Pediatric)

UCB INC Method for the treatment of Dravet syndrome
Nov, 2033

(9 years from now)

US9549909

(Pediatric)

UCB INC Method for the treatment of dravet syndrome
Nov, 2033

(9 years from now)

US9603814

(Pediatric)

UCB INC Method for the treatment of Dravet syndrome
Nov, 2033

(9 years from now)

US10478442

(Pediatric)

UCB INC Method for the treatment of Dravet Syndrome
Nov, 2033

(9 years from now)

US10478441

(Pediatric)

UCB INC Method for the treatment of Dravet syndrome
Nov, 2033

(9 years from now)

US10950331 UCB INC Control system for control of distribution of medication
Sep, 2035

(11 years from now)

US10950331

(Pediatric)

UCB INC Control system for control of distribution of medication
Mar, 2036

(11 years from now)

US10947183

(Pediatric)

UCB INC Fenfluramine compositions and methods of preparing the same
Jun, 2037

(13 years from now)

US11040018 UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Aug, 2037

(13 years from now)

US11406606 UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Aug, 2037

(13 years from now)

US11786487 UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Aug, 2037

(13 years from now)

US11759440 UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Aug, 2037

(13 years from now)

US10603290 UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Aug, 2037

(13 years from now)

US11406606

(Pediatric)

UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Feb, 2038

(13 years from now)

US11759440

(Pediatric)

UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Feb, 2038

(13 years from now)

US11786487

(Pediatric)

UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Feb, 2038

(13 years from now)

US10603290

(Pediatric)

UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Feb, 2038

(13 years from now)

US11040018

(Pediatric)

UCB INC Formulation for inhibiting formation of 5-HT2B agonists and methods of using same
Feb, 2038

(13 years from now)

US10452815 UCB INC Control system for control of distribution of medication
Jun, 2038

(14 years from now)

US10452815

(Pediatric)

UCB INC Control system for control of distribution of medication
Dec, 2038

(14 years from now)

Drug Exclusivity Drug Exclusivity Expiration
Orphan Drug Exclusivity(ODE-312) Jun 25, 2027
New Indication(I-887) Mar 25, 2025
Orphan Drug Exclusivity(ODE-393) Mar 25, 2029
New Product(NP) Jun 25, 2023
Pediatric Exclusivity(PED) Sep 25, 2029

Drugs and Companies using FENFLURAMINE HYDROCHLORIDE ingredient

Market Authorisation Date: 25 June, 2020

Treatment: Use in combination with stiripentol, valproate, and clobazam for the treatment of seizures associated with dravet syndrome; Use in combination with stiripentol for the treatment of seizures associated...

Dosage: SOLUTION;ORAL

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

FINTEPLA family patents

Family Patents

3. Fluxid patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6221392 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

US6024981 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

Drugs and Companies using FAMOTIDINE ingredient

Market Authorisation Date: 24 September, 2004

Treatment: NA

Dosage: TABLET, ORALLY DISINTEGRATING;ORAL

More Information on Dosage

FLUXID family patents

Family Patents

4. Kemstro patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6221392 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

US6024981 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

Drugs and Companies using BACLOFEN ingredient

Market Authorisation Date: 30 October, 2003

Treatment: NA

Dosage: TABLET, ORALLY DISINTEGRATING;ORAL

More Information on Dosage

KEMSTRO family patents

Family Patents

5. Keppra patents expiration

KEPPRA's oppositions filed in EPO
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8802142 UCB INC Pharmaceutical compositions comprising levetiracetam and process for their preparation
Jun, 2031

(7 years from now)

US8802142

(Pediatric)

UCB INC Pharmaceutical compositions comprising levetiracetam and process for their preparation
Dec, 2031

(7 years from now)

Drug Exclusivity Drug Exclusivity Expiration
New Patient Population(NPP) Dec 16, 2014
Pediatric Exclusivity(PED) Jun 16, 2015

Drugs and Companies using LEVETIRACETAM ingredient

Market Authorisation Date: 06 January, 2006

Treatment: NA

Dosage: TABLET;ORAL

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

KEPPRA family patents

Family Patents

6. Keppra Xr patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7858122 UCB INC Extended release formulation of levetiracetam
Sep, 2028

(4 years from now)

Drug Exclusivity Drug Exclusivity Expiration
New Dosage Form(NDF) Sep 12, 2011

Drugs and Companies using LEVETIRACETAM ingredient

Market Authorisation Date: 12 September, 2008

Treatment: NA

Dosage: TABLET, EXTENDED RELEASE;ORAL

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

KEPPRA XR family patents

Family Patents

7. Nayzilam patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US8809322 UCB INC Methods and compositions for the delivery of a therapeutic agent
Jan, 2028

(3 years from now)

US9289432 UCB INC Methods and compositions for the delivery of a therapeutic agent
Jan, 2028

(3 years from now)

US8217033 UCB INC Methods and compositions for the delivery of a therapeutic agent
Jan, 2028

(3 years from now)

US9687495 UCB INC Methods and systems for the delivery of a therapeutic agent
Jan, 2028

(3 years from now)

Drug Exclusivity Drug Exclusivity Expiration
Orphan Drug Exclusivity(ODE-243) May 17, 2026
New Product(NP) May 21, 2022

Drugs and Companies using MIDAZOLAM ingredient

Market Authorisation Date: 17 May, 2019

Treatment: Acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from a patient's usual seizure pattern in patie...

Dosage: SPRAY;NASAL

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

NAYZILAM family patents

Family Patents

8. Neupro patents expiration

NEUPRO's oppositions filed in EPO
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US7413747 UCB INC Transdermal therapeutic system for treating Parkinsonism
Mar, 2019

(5 years ago)

US6699498 UCB INC Transdermal therapeutic systems having improved stability and their production
Nov, 2020

(3 years ago)

US6884434 UCB INC Transdermal therapeutic system which contains a d2 agonist and which is provided for treating parkinsonism, and a method for the production thereof
Mar, 2021

(3 years ago)

US8617591 UCB INC Transdermal delivery system for the administration of rotigotine
Jul, 2023

(8 months ago)

US8246980 UCB INC Transdermal delivery system
Nov, 2025

(1 year, 7 months from now)

US8246979 UCB INC Transdermal delivery system for the administration of rotigotine
Sep, 2027

(3 years from now)

US10130589 UCB INC Polyvinylpyrrolidone for the stabilization of a solid dispersion of the non-crystalline form of rotigotine
Dec, 2030

(6 years from now)

US10350174 UCB INC Polyvinylpyrrolidone for the stabilization of a solid dispersion of the non-crystalline form of rotigotine
Dec, 2030

(6 years from now)

US9925150 UCB INC Polyvinylpyrrolidone for the stabilization of a solid dispersion of the non-crystalline form of rotigotine
Mar, 2032

(7 years from now)

Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) May 09, 2012
New Indication(I-647) Apr 02, 2015
New Indication(I-646) Apr 02, 2015

Drugs and Companies using ROTIGOTINE ingredient

NCE-1 date: 10 May, 2011

Market Authorisation Date: 02 April, 2012

Treatment: A method for the treatment of a patient suffering from a disease treatable with rotigotine, comprising applying the claimed transdermal delivery system (tds) to the skin of the patient; Treatment of s...

Dosage: FILM, EXTENDED RELEASE;TRANSDERMAL

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

NEUPRO family patents

Family Patents

9. Niravam patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US6024981 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

US6221392 UCB INC Rapidly dissolving robust dosage form
Apr, 2018

(6 years ago)

Drugs and Companies using ALPRAZOLAM ingredient

Market Authorisation Date: 19 January, 2005

Treatment: NA

Dosage: TABLET, ORALLY DISINTEGRATING;ORAL

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

NIRAVAM family patents

Family Patents

10. Vimpat patents expiration

VIMPAT Litigations
Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US5654301 UCB INC Amino acid derivative anticonvulsant
Aug, 2014

(9 years ago)

USRE38551 UCB INC Anticonvulsant enantiomeric amino acid derivatives
Mar, 2022

(2 years ago)

Drug Exclusivity Drug Exclusivity Expiration
New Dosing Schedule(D-188) Apr 28, 2026
New Patient Population(NPP) Oct 14, 2024
New Dosing Schedule(D-144) Aug 29, 2017
New Indication(I-696) Aug 29, 2017
New Dosing Schedule(D-143) Aug 29, 2017
New Indication(I-878) Nov 16, 2023
New Chemical Entity Exclusivity(NCE) Oct 28, 2013

Drugs and Companies using LACOSAMIDE ingredient

NCE-1 date: 28 October, 2012

Market Authorisation Date: 28 October, 2008

Treatment: Method of treating, as adjunctive therapy, partial-onset seizures in a patient with epilepsy aged 17 years and older; Method of use for treatment of partial-onset seizures in patients 4 years of age a...

Dosage: TABLET;ORAL; SOLUTION;INTRAVENOUS; SOLUTION;ORAL

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

VIMPAT family patents

Family Patents

11. Zilbrysq patents expiration

Drug Patent Number Company Drug Patent Title Drug Patent Expiry Activity Alert
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance.
US10562934 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

US10208089 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

US10106579 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

US10435438 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

US11014965 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US11752190 UCB INC Modulators of complement activity
Jun, 2035

(11 years from now)

US10835574 UCB INC Modulators of complement activity
Jun, 2035

(11 years from now)

US11535650 UCB INC Modulation of complement activity
Jun, 2035

(11 years from now)

Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Oct 17, 2028
Orphan Drug Exclusivity(ODE-446) Oct 17, 2030

Drugs and Companies using ZILUCOPLAN SODIUM ingredient

NCE-1 date: 18 October, 2027

Market Authorisation Date: 17 October, 2023

Treatment: Treatment of generalized myasthenia gravis (gmg) in an adult patient who is anti-acetylcholine receptor (achr) antibody positive by subcutaneous administration of c5 complement inhibitor zilucoplan

Dosage: SOLUTION;SUBCUTANEOUS

More Information on Dosage

ZILBRYSQ family patents

Family Patents