IP Library › Granted Patent US 10,730,883
Granted Patent B2
US 10,730,883 · App. 16/787,251 · Granted Aug 4, 2020

Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof

Inventors: Ayman Allian (Newbury Park, CA); Jayanthy Jayanth (Buffalo, IL); Ben Klünder (Ludwigshafen, DE); Mohamed-Eslam F. Mohamed (Gurnee, IL); Ahmed A. Othman (Waukegan, IL); Patrick J. Marroum (Springfield, VA); Peter T. Mayer (Libertyville, IL)
Assignee: AbbVie Inc.
C07D487/14A61K9/0053A61K31/4985A61K47/12A61K47/38C07B2200/13
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Quick Facts
Patent No.
US 10,730,883
App. No.
16/787,251
Granted
Aug 4, 2020
Kind
B2
Abstract

The present disclosure relates to processes for preparing (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide, solid state forms thereof, and corresponding pharmaceutical compositions, methods of treatment (including treatment of rheumatoid arthritis), kits, methods of synthesis, and products-by-process.

Claims (8)

1. An oral extended-release solid dosage form comprising (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide in an amount sufficient to deliver 30 mg of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide free base equivalent, wherein oral administration of a single 30 mg dose of the solid dosage form to healthy adult subjects under fasting conditions results in a mean AUC inf from about 453 ng·hours/mL to about 660 ng·hours/mL, and a mean C max from about 55 ng/mL to about 85 ng/m L, of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide.

2. The solid dosage form of claim 1 , wherein the administration results in a mean C max from about 55 ng/mL to about 70 ng/mL.

3. The solid dosage form of claim 1 , wherein the administration results in a T max from about 1.0 hour to about 4.0 hours of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide.

4. The solid dosage form of claim 3 , wherein the median T max is about 2.0 hours.

5. An oral extended-release solid dosage form comprising (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide in an amount sufficient to deliver 30 mg of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide free base equivalent, wherein the solid dosage form is bioequivalent to an oral extended-release film-coated tablet consisting of:

(i) in the intragranular core: 30.7 mg of Freebase Hydrate Form C, 79.9 mg of microcrystalline cellulose, and 9.5 mg of hydroxypropyl methyl cellulose;

(ii) in the extragranular core: 67.2 mg of microcrystalline cellulose, 100.6 mg of mannitol, 96.0 mg of tartaric acid, 86.5 mg of hydroxypropyl methyl cellulose, 2.4 mg of colloidal silicon dioxide/silica, and 7.2 mg of magnesium stearate; and

(iii) 14.4 mg of a film coat comprising polyvinyl alcohol, titanium dioxide, polyethylene glycol 3350, talc, and iron oxide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2020
From: KLÜNDER, BEN
To: ABBVIE DEUTSCHLAND GMBH & CO. KG
Reel/Frame 052892/0346 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2020
From: ABBVIE DEUTSCHLAND GMBH & CO. KG
To: ABBVIE INC.
Reel/Frame 052892/0495 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2020
From: ALLIAN, AYMAN; JAYANTH, JAYANTHY; MOHAMED, MOHAMED-ESLAM F.; OTHMAN, AHMED A.; MARROUM, PATRICK J.; MAYER, PETER T.
To: ABBVIE INC.
Reel/Frame 052853/0785 →
Continuity (10)
Continuation 16656237 · Oct 17, 2019
Continuation 16458622 · Jul 1, 2019
Continuation 15891012 · Feb 7, 2018
Continuation 15891012 · Feb 7, 2018
Continuation 15295561 · Oct 17, 2016
Provisional Application 62352380 · Jun 20, 2016
Provisional Application 62301537 · Feb 29, 2016
Provisional Application 62267672 · Dec 15, 2015
Provisional Application 62242797 · Oct 16, 2015
Related Publication 20200181158A1 · Jun 11, 2020
Cited By (1)
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