Average Co-Inventor Count = 9.66
ph-index = 8
The patent ph-index is calculated by counting the number of publications for which an author has been cited by other authors at least that same number of times.
Company Filing History:
1. Merck Sharp + Dohme Corp. (18 from 2,405 patents)
2. Lycera Corporation (6 from 36 patents)
18 patents:
1. 11174248 - Indazolyl-spiro[2.3]hexane-carbonitrile derivatives as LRRK2 inhibitors, pharmaceutical compositions, and uses thereof
2. 11161854 - Indazolyl-spiro[2.2]pentane-carbonitrile derivatives as LRRK2 inhibitors, pharmaceutical compositions, and uses thereof
3. 10745364 - Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
4. 10689369 - Substituted indazole compounds as RORgammaT inhibitors and uses thereof
5. 10584121 - Heteroaryl substituted benzoic acids as RORgammaT inhibitors and uses thereof
6. 10377768 - Tetrahydronaphthyridine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
7. 10344000 - Substituted bicyclic pyrazole compounds as RORgammaT inhibitors and uses thereof
8. 10287272 - Substituted indazole compounds as RORgammaT inhibitors and uses thereof
9. 10221142 - Substituted pyrazole compounds as RORgammaT inhibitors and uses thereof
10. 10221146 - Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
11. 10196354 - 4-heteroaryl substituted benzoic acid compounds as RORgammaT inhibitors and uses thereof
12. 9809561 - Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
13. 9745265 - 4-heteroaryl substituted benzoic acid compounds as RORgammaT inhibitors and uses thereof
14. 9663502 - 2-Acylamidomethyl and sulfonylamidomethyl benzoxazine carbamates for inhibition of RORgamma activity and the treatment of disease
15. 9663522 - 3-aminocycloalkyl compounds as RORgammaT inhibitors and uses thereof