IP Library Patent Application 14131282
Patent Application
App. No. 14/131,282

DARUNAVIR COMBINATION FORMULATIONS

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Quick Facts
Patent No.
US None
App. No.
14/131,282
Abstract

This invention relates to solid oral dosage forms of the HIV inhibitor Darunavir and/or a pharmaceutically acceptable salt or solvate thereof, and combination formulations thereof.

Claims (16)

1 . An oral dosage form comprising about 0.4 to 0.6% by weight (w/w) of a lubricant, about 3% by weight (w/w) of a disintegrant, 17 to 20% by weight (w/w) of silicon dioxide loaded with GS-9350 corresponding to a total amount of about 150 mg free form equivalent of GS-9350 and about 50 to 60% by weight (w/w) of darunavir granulate, said darunavir granulate consisting of darunavir and/or a pharmaceutically acceptable salt or solvate thereof, Hypromellose and any residual water from the granulation.

2 . An oral dosage form according to claim 1 , wherein the silicon dioxide loaded with GS-9350 is colloidal silicon dioxide.

3 . An oral dosage form according to claim 1 , wherein the Hypromellose is Hypromellose 2910 15 mPa·s.

4 . An oral dosage form according to claim 1 , comprising about 0.5% by weight (w/w) of a lubricant

5 . An oral dosage form according to claim 1 , wherein the desintegrant is polyplasdone XL-10 and the lubricant is magnesium stearate

6 . An oral dosage form according to claim 1 , comprising about 800 mg free form equivalent of Darunavir.

7 . A process for preparing an oral dosage form as claimed in claim 1 which comprises the steps of:

Providing granulated darunavir by; mixing water and Hypromellose, spraying this first mixture on a powder of darunavir and/or a pharmaceutically acceptable salt or solvate thereof, and drying the so obtained darunavir granulate

Providing a second mixture comprising microcrystalline cellulose, silicon dioxide loaded with GS-9350, a disintegrant,

Adding granulated darunavir to the mixture and subsequent dry-blending

Adding a lubricant and mixing until homogeneous,

Compressing the mixture to provide the oral dosage form, said oral dosage form then being optionally film-coated.

8 . A process for preparing an oral dosage form according to claim 7 , wherein the silicon dioxide loaded with GS-9350 is colloidal silicon dioxide.

9 . An oral dosage form as claimed in claim 1 for use in medicine.

10 . An oral dosage form as claimed in claim 1 for use in the treatment of HIV infection.

11 . A method for the treatment of an HIV infection in a subject which comprises administering to the subject an effective amount of an oral dosage form as claimed in claim 1 .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2015
From: JANSSEN R & D IRELAND
To: JANSSEN SCIENCES IRELAND UC
Reel/Frame 035496/0382 →
CORRECTIVE ASSIGNMENT TO CORRECT THE COMMA OMITTED IN ASSIGNEE NAME PREVIOUSLY RECORDED AT REEL: 031928 FRAME: 0343. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 12, 2015
From: JANSSEN R&D IRELAND (FORMERLY KNOWN AS TIBOTEC PHARMACEUTICALS); JANSSEN PHARMACEUTICA NV
To: JANSSEN R&D IRELAND (FORMERLY KNOWN AS TIBOTEC PHARMACEUTICALS); GILEAD SCIENCES, INC.
Reel/Frame 035197/0441 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2014
From: DELAET, URBAIN ALFONS C.; HEYNS, PHILIP ERNA H.; JANS, EUGEEN MARIA JOZEF; MERTENS, ROEL JOS M.; AVOORT, GEERT VAN DER
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 031928/0277 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2014
From: JANSSEN PHARMACEUTICA NV
To: JANSSEN R&D IRELAND (FORMERLY KNOWN AS TIBOTEC PHARMACEUTICALS); GILEAD SCIENCES
Reel/Frame 031928/0343 →