IP Library Granted Patent US 10,093,691
Granted Patent B2
US 10,093,691 · App. 15/288,139 · Granted Oct 9, 2018

Crystallization method and bioavailability

Inventors: Mazen Hanna (Lutz, FL); Ning Shan (Tampa, FL); Miranda L. Cheney (Bishops Quay, IE); David R. Weyna (Lutz, FL); Raymond Houck (Oakmont, PA)
Assignee: GRUNENTHAL GMBH
C07F9/65061A61K31/675C07C229/08C07C229/26C07D213/82C07D473/34C07B2200/13
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Quick Facts
Patent No.
US 10,093,691
App. No.
15/288,139
Granted
Oct 9, 2018
Kind
B2
Abstract

Preparation and in vitro and in vivo characterization of novel forms of active pharmaceutical ingredients, suitable for pharmaceutical compositions in drug delivery systems for humans.

Claims (8)

1. A pharmaceutical composition comprising a crystalline molecular complex comprising zoledronic acid, sodium zoledronate, and water and a pharmaceutically acceptable excipient,

wherein the crystalline molecular complex is characterized by a powder x-ray diffraction pattern having peaks at about 8.1, 13.3, 21.5, 24.6, and 25.6±0.2 degrees two-theta, a powder x-ray diffraction pattern as shown in FIG. 1 , or a Fourier transform infrared spectroscopy pattern as shown in FIG. 2 .

2. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is a unit dose;

wherein the unit dose comprises between about 1 mg to about 500 mg, about 10 mg to about 400 mg, about 10 mg to about 300 mg, about 10 mg to about 200 mg, or about 10 mg to about 100 mg of the zoledronic acid.

3. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is an oral dosage form;

wherein the oral dosage form is an enteric coated tablet, an enteric coated caplet, an enteric coated capsule, an enterically coated soft gelatin capsule, or an enterically coated hard gelatin capsule.

4. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated as a sustained release formulation, an immediate release formulation, a delayed+sustained release formulation, an enteric release formulation, modified enteric release formulation, or a biphasic release formulation.

5. A method for the treatment of disease states associated with osteoporosis, hypercalcemia, cancer induced bone metastasis, Paget's disease, adjuvant cancer therapy, or neoadjuvant cancer therapy comprising the step of administering the pharmaceutical composition of claim 1 daily, twice weekly, weekly, or with a time between doses of 10 days, two weeks, three weeks, four weeks, six weeks, eight weeks, or two months.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2019
From: GRUNENTHAL GMBH
To: THAR PHARMA, LLC
Reel/Frame 050762/0370 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2017
From: THAR PHARMACEUTICALS, INC.
To: GRUNENTHAL GMBH
Reel/Frame 041224/0125 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2016
From: HANNA, MAZEN; SHAN, NING; CHENEY, MIRANDA L.; WEYNA, DAVID R.; HOUCK, RAYMOND
To: THAR PHARMACEUTICALS, INC.
Reel/Frame 039993/0200 →
Continuity (21)
Continuation 14730843 · Jun 4, 2015
Continuation 13567827 · Aug 6, 2012
Continuation In Part 12847568 · Jul 30, 2010
Continuation In Part 13387490
Continuation In Part PCTUS2011023427 · Feb 2, 2011
Continuation In Part 12847568 · Jul 30, 2010
Continuation In Part PCTUS2010043916 · Jul 30, 2010
Continuation In Part PCTUS2010043892 · Jul 30, 2010
Provisional Application 61230222 · Jul 31, 2009
Provisional Application 61288036 · Dec 18, 2009
Provisional Application 61302110 · Feb 6, 2010
Provisional Application 61312879 · Mar 11, 2010
Provisional Application 61318503 · Mar 29, 2010
Provisional Application 61359544 · Jun 29, 2010
Provisional Application 61230234 · Jul 31, 2009
Provisional Application 61333041 · May 10, 2010
Provisional Application 61333028 · May 10, 2010
Provisional Application 61379814 · Sep 3, 2010
Provisional Application 61455778 · Oct 26, 2010
Provisional Application 61522116 · Aug 10, 2011
Related Publication 20170022227A1 · Jan 26, 2017