IP Library Granted Patent US 10,487,060
Granted Patent B2
US 10,487,060 · App. 15/896,779 · Granted Nov 26, 2019

5-[(piperazin-1-yl)-3-oxo-propyl]-imidazolidine-2,4-dione derivatives as ADAMTS inhibitors for the treatment of osteoarthritis

Inventors: Franck Laurent Brebion (Romainville, FR); Luke Jonathan Alvey (Romainville, FR); David Amantini (Romainville, FR); Frédéric André De Ceuninck (Paris, FR); Pierre Marc Marie Joseph Deprez (Romainville, FR); Romain Luc Marie Gosmini (Romainville, FR); Hélène Marie Jary (Romainville, FR); Christophe Peixoto (Romainville, FR); Iuliana Ecaterina Pop-Botez (Houilles, FR); Marie Laurence Claire Varin (Romainville, FR)
Assignees: GALAPAGOS NV; LES LABORATOIRES SERVIER
C07D233/78A61K31/496A61K31/5377A61K31/55C07D401/04C07D401/12C07D401/14C07D403/06C07D403/14C07D405/12C07D417/12
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Quick Facts
Patent No.
US 10,487,060
App. No.
15/896,779
Granted
Nov 26, 2019
Kind
B2
Abstract

The present invention discloses compounds according to Formula I: Wherein R 1 , R 2 , R 3a , R 3b , and Cy are as defined herein. The present invention relates to compounds inhibiting ADAMTS, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of inflammatory conditions, and/or diseases involving degradation of cartilage and/or disruption of cartilage homeostasis by administering a compound of the invention.

Claims (222)

1. A method of treating and/or preventing osteoarthritis comprising administering to a subject in need thereof, a compound according to Formula I:

wherein

R 1 is:

H,

C 1-4 alkyl optionally substituted with one or more independently selected R 4 groups,

C 3-7 monocyclic cycloalkyl optionally substituted with one or more independently selected R 4 groups,

4-7 membered monocyclic heterocycloalkyl comprising 1 to 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected C 1-4 alkyl, —C(═O)C 1-4 alkyl, or —C(═O)OC 1-4 alkyl,

phenyl optionally substituted with one or more independently selected R 5 groups,

phenyl fused to a 5-6 membered monocyclic heterocycloalkyl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, which heterocycloalkyl is optionally substituted with one or more ═O,

5-6 membered monocyclic heteroaryl comprising 1 or 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected R 5 groups;

R 2 is independently selected from:

H,

OH,

C 1-4 alkoxy, or

C 1-4 alkyl optionally substituted with one

OH,

—CN,

C 1-4 alkoxy optionally substituted with one phenyl, or

5-6 membered monocyclic heteroaryl comprising 1 or 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected C 1-4 alkyl;

each R 3a , and R 3b is independently selected from:

H, or

C 1-4 alkyl;

Cy is

6-10 membered monocyclic or fused bicyclic aryl optionally substituted with one or more independently selected R 6 groups,

5-10 membered monocyclic or fused bicyclic heteroaryl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected R 6 groups;

R 4 is

halo,

OH,

—CN,

C 1-4 alkyl,

C 1-4 alkoxy optionally substituted with C 1-4 alkoxy, or phenyl,

C 1-4 thioalkoxy,

4-7-membered monocyclic heterocycloalkyl comprising one or more heteroatoms independently selected from N, S, or O, optionally substituted with one or more halo, or —C(═O)OC 1-4 alkyl,

phenyl,

—S(═O) 2 C 1-4 alkyl

—C(═OR 7a

—C(═O)NR 7b R 7c

—NHC(═O)OR 7d

—NHC(═O)R 7e , or

NR 8a R 8b ;

each R 5 is

halo,

OH,

—CN,

C 1-4 alkyl optionally substituted with one or more independently selected halo, —NR 9a R 9b , or —C(═O)NR 9c R 9d ,

C 1-4 alkoxy optionally substituted with —NR 9e R 9f , or

—S(═O) 2 C 1-4 alkyl;

each R 6 is

halo,

—CN,

—NO 2 ,

—CH 3 ,

5-10 membered monocyclic or fused bicyclic heteroaryl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected halo, C 1-4 alkyl, or C 1-4 alkoxy, or

—NR 9g R 9h ;

each R 7a , R 7b , R 7c , R 7d , or R 7e , is

H, or

C 1-4 alkyl optionally substituted with OH, or C 1-4 alkoxy;

each R 8a , or R 8b is independently selected from

H, or

C 1-4 alkyl optionally substituted with OH, C 1-4 alkoxy, or phenyl:

each R 9a , R 9b , R 9c , R 9d , R 9e , R 9f , R 9g , and R 9h is independently selected from H, or C 1-4 alkyl;

or a pharmaceutically acceptable salt thereof;

provided that:

R 1 and R 2 are not simultaneously H, and when R 1 is Me, and R 2 is H, then Cy is not

or a pharmaceutically acceptable salt thereof.

2. The method according to claim 1 , wherein the compound has Formula II:

wherein R 1 , R 2 , R 3a , R 3b , and Cy are as defined in claim 1 .

3. The method according to claim 1 , wherein R 1 is H.

4. The method according to claim 1 , wherein R 1 is C 1-4 alkyl.

5. The method according to claim 1 , wherein R 1 is C 3-7 monocyclic cycloalkyl.

6. The method according to claim 1 , wherein the compound has Formula IIIa or IIIb:

wherein R 2 , R 3a , R 3b and Cy are as described in claim 1 .

7. The method according to claim 1 , wherein R 2 is C 1-4 alkyl.

8. The method according to claim 1 , wherein the compound has Formula IVa or IVb:

wherein R 3a , R 3b and Cy are as described in claim 1 .

9. The method according to claim 1 , wherein each R 3a , and R 3b is independently selected from H or CH 3 .

10. The method according to claim 1 , wherein Cy is 6-10 membered aryl, substituted with one or more independently selected R 6 groups.

11. The method according to claim 1 , wherein Cy is phenyl substituted with one or more independently selected R 6 groups.

12. The method according to claim 10 , wherein each R 6 is F, Cl, CN, CH 3 , or NO 2 .

13. The method according to claim 1 , wherein the compound is 5-[3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chloro-5-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

(5S)-5-cyclopropyl-5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

(5S)-5-cyclopropyl-5-[(2S)-3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(4-chlorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[4-(3,4-difluorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione,

5-[2-[4-(3,5-dichlorophenyl)piperazine-1-carbonyl]butyl]-5-methyl-imidazolidine-2,4-dione,

(S)-5-((S)-3-((S)-4-(3-chloro-4-fluorophenyl)-3-methylpiperazin-1-yl) -2-methyl-3-oxopropyl)-5-(methoxymethyl)imidazolidine-2,4-dione,

5-[3-[4-(3-chlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[4-(3-chloro-2-methyl-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

tert-butyl N-[2-[4-[3-[4-(3,4-difluorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-2,5-dioxo-imidazolidin-4-yl]ethyl]carbamate,

(5S)-5-cyclopropyl-5-[3-(3S)-4-(3,5-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

(5R)-5-[(2S)-3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-methyl-imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-[3-fluoro-5-(1H-pyrazol-4-yl)phenyl]-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-(hydroxymethyl)-3-oxo-propyl]-5-methyl-imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chlorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[(3S)-4-(4-chloro-3,5-difluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-methyl-imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-methylsulfonylethyl)imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

(5S)-cyclopropyl-5-[3-[(3S)-4-(3,5-difluorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-fluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[4-(4-chloro-3,5-difluoro-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[4-(5-fluoro-2-methyl-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione, or

5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione.

14. The method according to claim 1 , wherein the compound or pharmaceutically acceptable salt thereof is formulated as a medicament.

15. A method of treating and/or preventing osteoarthritis comprising administering to a subject in need thereof, a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound according to Formula I:

wherein

R 1 is:

H,

C 1-4 alkyl optionally substituted with one or more independently selected R 4 groups,

C 3-7 monocyclic cycloalkyl optionally substituted with one or more independently selected R 4 groups,

4-7 membered monocyclic heterocycloalkyl comprising 1 to 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected C 1-4 alkyl, —C(═O)C 1-4 alkyl, or —C(═O)OC 1-4 alkyl,

phenyl optionally substituted with one or more independently selected R 5 groups,

phenyl fused to a 5-6 membered monocyclic heterocycloalkyl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, which heterocycloalkyl is optionally substituted with one or more ═O,

5-6 membered monocyclic heteroaryl comprising 1 or 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected R 5 groups:

R 2 is independently selected from:

H,

OH,

C 1-4 alkoxy, or

C 1-4 alkyl optionally substituted with one

OH,

—CN,

C 1-4 alkoxy optionally substituted with one phenyl, or

5-6 membered monocyclic heteroaryl comprising 1 or 2 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected C 1-4 alkyl;

each R 3a , and R 3b is independently selected from:

H, or

C 1-4 alkyl:

Cy is

6-10 membered monocyclic or fused bicyclic aryl optionally substituted with one or more independently selected R 6 groups,

5-10 membered monocyclic or fused bicyclic heteroaryl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected R 6 groups;

R 4 is

halo,

OH,

—CN,

C 1-4 alkyl,

C 1-4 alkoxy optionally substituted with C 1-4 alkoxy, or phenyl,

C 1-4 thioalkoxy,

4-7-membered monocyclic heterocycloalkyl comprising one or more heteroatoms independently selected from N, S, or 0, optionally substituted with one or more halo, or —C(═O)OC 1-4 alkyl,

phenyl,

—S(═O) 2 C 1-4 alkyl

—C(═O)OR 7a

—C(═O)NR 7b R 7c

—NHC(═O)OR 7d

—NHC(═O)R 7e , or

—NR 8a R 8b ;

each R 5 is

halo,

OH,

—CN,

C 1-4 alkyl optionally substituted with one or more independently selected halo, —NR 9a R 9b , or —C(═O)NR 9c R 9d ,

C 1-4 alkoxy optionally substituted with —NR 9e R 9f , or

—S(═O) 2 C 1-4 alkyl;

each R 6 is

halo,

—CN,

—NO 2

—CH 3

5-10 membered monocyclic or fused bicyclic heteroaryl comprising 1, 2 or 3 heteroatoms independently selected from N, O, or S, optionally substituted with one or more independently selected halo, C 1-4 alkyl, or C 1-4 alkoxy, or

—NR 9g R 9h ;

each R 7a , R 7b , R 7c , R 7d , or R 7e , is

H, or

C 1-4 alkyl optionally substituted with OH, or C 1-4 alkoxy;

each R 8a , or R 8b is independently selected from

H, or

C 1-4 alkyl optionally substituted with OH, C 1-4 alkoxy, or phenyl;

each R 9a , R 9b , R 9c , R 9d , R 9e , R 9f , R 9g , and R 9h is independently selected from H, or C 1-4 alkyl;

or a pharmaceutically acceptable salt thereof;

provided that:

R 1 and R 2 are not simultaneously H, and

when R 1 is Me, and R 2 is H, then Cy is not

or a pharmaceutically acceptable salt thereof.

16. The method according to claim 15 , further comprising administering a second therapeutic agent.

17. The method according to claim 15 , wherein the compound has Formula II:

wherein R 1 , R 2 , R 3a , R 3b , and Cy are as defined in claim 15 .

18. The method of claim 15 , wherein R 1 is H.

19. The method of claim 15 , wherein R 1 is C 1-4 alkyl.

20. The method of claim 15 , wherein R 1 is C 3-7 monocyclic cycloalkyl.

21. The method of claim 15 , wherein the compound has Formula IIIa or IIIb:

wherein R 2 , R 3a , R 3b and Cy are as described in claim 15 .

22. The method of claim 15 , wherein R 2 is C 1-4 alkyl.

23. The method of claim 15 , wherein the compound has Formula IVa or IVb:

wherein R 3a , R 3b and Cy are as described in claim 15 .

24. The method of claim 15 , wherein each R 3a , and R 3b is independently selected from H or CH 3 .

25. The method of claim 15 , wherein Cy is 6-10 membered aryl, substituted with one or more independently selected R 6 groups.

26. The method of claim 15 , wherein Cy is phenyl substituted with one or more independently selected R 6 groups.

27. The method of claim 25 , wherein each R 6 is F, Cl, CN, CH 3 , or NO 2 .

28. The method of claim 15 , wherein the compound is

5-[3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chloro-5-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

(5S)-5-cyclopropyl-5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

(5S)-5-cyclopropyl-5-[(2S)-3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(4-chlorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[4-(3,4-difluorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione,

5-[2-[4-(3,5-dichlorophenyl)piperazine-1-carbonyl]butyl]-5-methyl-imidazolidine-2,4-dione,

(S)-5-((S)-3-((S)-4-(3-chloro-4-fluorophenyl)-3-methylpiperazin-1 -yl)-2-methyl-3-oxopropyl)-5-(methoxymethyl)imidazolidine-2,4-dione,

5-[3-[4-(3-chlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

5-[3-[4-(3-chloro-2-methyl-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-cyclopropyl-imidazolidine-2,4-dione,

tert-butyl N-[2-[4-[3-[4-(3,4-difluorophenyl)piperazin-1 -yl]-2-methyl-3-oxo-propyl]-2,5-dioxo-imidazolidin-4-yl]ethyl]carbamate,

(5S)-5-cyclopropyl-5-[3-[(3S)-4-(3,5-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

(5R)-5-[(2S)-3-[(3S)-4-(3-chloro-4-fluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-methyl-imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-[3-fluoro-5-(1H-pyrazol-4-yl)phenyl]-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-(hydroxymethyl)-3-oxo -propyl]-5-methyl-imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3,4-difluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-chlorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[(3S)-4-(4-chloro-3,5-difluoro-phenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-methyl-imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-methylsulfonylethyl)imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

(5S)-cyclopropyl-5-[3-[(3S)-4-(3,5-difluorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[(3S)-4-(3-fluorophenyl)-3-methyl-piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione,

5-[3-[4-(4-chloro-3,5-difluoro-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione,

5-cyclopropyl-5-[3-[4-(5-fluoro-2-methyl-phenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]imidazolidine-2,4-dione,

5-[3-[4-(3,5-dichlorophenyl)piperazin-1-yl]-2-methyl-3-oxo-propyl]-5-(methoxymethyl)imidazolidine-2,4-dione, or

5-[3-[(3S)-4-(3,4-dichlorophenyl)-3-methyl-piperazin-1-yl]-3-oxo-propyl]-5-(2-pyridyl)imidazolidine-2,4-dione.

Assignments (6)
CHANGE OF NAME Recorded Jun 4, 2026
From: GALAPAGOS
To: LAKEFRONT BIOTHERAPEUTICS
Reel/Frame 074845/0068 →
RELEASE OF SECURITY INTEREST Recorded Feb 15, 2022
From: GILEAD SCIENCES, INC.
To: GALAPAGOS NV
Reel/Frame 059020/0871 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2021
From: LES LABORATOIRES SERVIER
To: GALAPAGOS NV
Reel/Frame 057442/0384 →
SECURITY INTEREST Recorded Aug 23, 2019
From: GALAPAGOS NV
To: GILEAD SCIENCES, INC.
Reel/Frame 050149/0161 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2018
From: BREBION, FRANCK LAURENT; AMANTINI, DAVID; DEPREZ, PIERRE MARC MARIE JOSEPH; GOSMINI, ROMAIN LUC MARIE; JARY, HÉLÈNE MARIE; PEIXOTO, CHRISTOPHE; VARIN, MARIE LAURENCE CLAIRE; ALVEY, LUKE JONATHAN
To: GALAPAGOS NV
Reel/Frame 046317/0233 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2018
From: DE CEUNINCK, FRÉDÉRIC ANDRÉ; POP-BOTEZ, IULIANA ECATERINA
To: LES LABORATOIRES SERVIER
Reel/Frame 046317/0573 →
Priority Claims (1)
EP 14307129 · Dec 22, 2014 · regional
Continuity (2)
Continuation 15538393
Related Publication 20180258052A1 · Sep 13, 2018