IP Library Granted Patent US 10,500,202
Granted Patent B2
US 10,500,202 · App. 15/827,417 · Granted Dec 10, 2019

Pharmaceutical formulation containing tadalafil

Inventors: Betti Szabóné Ordasi (Budapest, HU); Tamás Jordán (Öcsöd, HU); Richárd Balázs Kárpáti (Tatabánya, HU); Andrea Ujhelyi (Nyiregyhaza, HU); Tamás Solymosi (Békéscsaba, HU); Hristos Glavinas (Szeged, HU); Genovéva Filipcsei (Budapest, HU)
Assignee: Druggability Technologies IP Holdco Limited
A61K31/4985A61K9/1617A61K9/1635A61K9/1682A61K9/19A61K47/20A61K47/32A61P9/12A61P13/08A61P15/10A61P21/00
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Quick Facts
Patent No.
US 10,500,202
App. No.
15/827,417
Granted
Dec 10, 2019
Kind
B2
Abstract

Disclosed herein are pharmaceutical compositions comprising Tadalafil, or a salt, or derivatives thereof and pharmaceutical excipients, processes for the preparation thereof, and pharmaceutical compositions containing them. The pharmaceutical compositions have improved physicochemical properties that provide faster onset of action for the treatment of erectile dysfunction.

Claims (15)

1. A pharmaceutical composition comprising

10-40% by weight of Tadalafil or a salt thereof;

35-70% by weight of a primary pharmaceutical excipient which is copovidone (copolymer of vinylpyrrolidone and vinyl acetate); and

5-50% by weight of a secondary pharmaceutical excipient which is sodium lauryl sulfate;

wherein said pharmaceutical composition is obtained by a process comprising mixing followed by spray-drying;

wherein said pharmaceutical composition has a controlled particle size in the range between 10 nm and 500 nm; and

wherein said pharmaceutical composition shows X-ray amorphous character in the solid form.

2. The pharmaceutical composition as recited in claim 1 , wherein said composition is characterized by said Raman spectrum as shown in FIG. 7 .

3. The pharmaceutical composition as recited in claim 1 , wherein said particle size is between 10 nm and 200 nm.

4. The pharmaceutical composition as recited in claim 1 , wherein said pharmaceutical composition shows a t max of 0.5-0.75 hours.

5. The pharmaceutical composition as recited in claim 1 , wherein said pharmaceutical composition has a dissolution profile such that about 60% of the pharmaceutical composition is dissolved in simulated gastric fluid over two hours.

6. A pharmaceutical dosage form comprising the pharmaceutical composition according to claim 1 , together with pharmaceutically acceptable excipients.

7. The pharmaceutical dosage form comprising the pharmaceutical composition according to claim 6 , wherein said pharmaceutical dosage form is suitable for oral administration.

8. The pharmaceutical composition as recited in claim 1 , wherein the pharmaceutical composition has an apparent solubility in water of at least 0.7 mg/mL.

9. The pharmaceutical composition as recited in claim 1 , wherein the pharmaceutical composition has a PAMPA permeability of at least 4×10 −6 cm/s when dispersed in water, FaSSIF or FeSSIF biorelevant media, which does not decrease in time at least for 6 months.

Assignments (3)
MERGER Recorded Feb 18, 2021
From: DRUGGABILITY TECHNOLOGIES IP HOLDCO LIMITED
To: NANGENEX NANOTECHNOLOGY INCORPORATED
Reel/Frame 055321/0877 →
CHANGE OF NAME Recorded Feb 18, 2021
From: NANGENEX NANOTECHNOLOGY INCORPORATED
To: TAVANTA THERAPEUTICS HUNGARY INCORPORATED
Reel/Frame 055322/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2018
From: SZABÓNÉ ORDASI, BETTI; JORDÁN, TAMÁS; KÁRPÁTI, RICHÁRD BALÁZS; UJHELYI, ANDREA; SOLYMOSI, TAMÁS; GLAVINAS, HRISTOS; FILIPCSEI, GENOVÉVA
To: DRUGGABILITY TECHNOLOGIES IP HOLDCO LIMITED
Reel/Frame 045592/0879 →
Continuity (4)
Provisional Application 62502157 · May 5, 2017
Provisional Application 62438539 · Dec 23, 2016
Provisional Application 62428309 · Nov 30, 2016
Related Publication 20180161325A1 · Jun 14, 2018