IP Library Granted Patent US 8,530,485
Granted Patent B2
US 8,530,485 · App. 13/076,220 · Granted Sep 10, 2013

Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors

Inventors: James D. Rodgers (Landenberg, PA); Stacey Shepard (Wilmington, DE)
Assignee: Incyte Corporation
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Quick Facts
Patent No.
US 8,530,485
App. No.
13/076,220
Granted
Sep 10, 2013
Kind
B2
Abstract

The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.

Claims (10)

1. A pharmaceutical composition comprising a compound, which is 3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier; wherein said composition is suitable for oral administration and for providing sustained release of said compound or said salt.

2. The pharmaceutical composition of claim 1 , wherein the compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof.

3. The pharmaceutical composition of claim 2 , wherein said composition is a unit dosage form.

4. The pharmaceutical composition of claim 3 , wherein said unit dosage form is a tablet.

5. The pharmaceutical composition of claim 3 , wherein said unit dosage form is a capsule.

6. The pharmaceutical composition of claim 3 , wherein said unit dosage form further comprises an enteric coating.

7. The pharmaceutical composition according to claim 3 , wherein the unit dosage form comprises from about 5 to about 1000 mg of said compound or said salt.

8. The pharmaceutical composition according to claim 2 , further comprising one or more excipients selected from lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, and methyl cellulose.

9. The pharmaceutical composition according to claim 2 , further comprising microcrystalline cellulose.

10. The pharmaceutical composition according to claim 2 , further comprising lactose.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE OMMISSION OF SECOND RECEIVING PARTY NAME PREVIOUSLY RECORDED AT REEL: 035292 FRAME: 0004. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 2, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION; INCYTE CORPORATION
Reel/Frame 036054/0696 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION AND INCYTE CORPORATION
Reel/Frame 035924/0004 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2011
From: RODGERS, JAMES D.; SHEPARD, STACEY; MADUSKUIE, THOMAS P.; WANG, HAISHENG; FALAHATPISHEH, NIKOO; RAFALSKI, MARIA; ARVANITIS, ARGYRIOS G.; STORACE, LOUIS; JALLURI, RAVI KUMAR; FRIDMAN, JORDAN S.; VADDI, KRISHNA
To: INCYTE CORPORATION
Reel/Frame 026519/0803 →
Continuity (8)
Continuation 12549170 · Aug 27, 2009
Continuation 11637545 · Dec 12, 2006
Provisional Application 60749905 · Dec 13, 2005
Provisional Application 60810231 · Jun 2, 2006
Provisional Application 60850625 · Oct 10, 2006
Provisional Application 60856872 · Nov 3, 2006
Provisional Application 60859404 · Nov 16, 2006
Related Publication 20110223210A1 · Sep 15, 2011