Abstract: The invention relates to pharmaceutical compositions comprising rivaroxaban, suitable for immediate release, and processes of preparing such compositions, preferably by a melt-granulation process or by a specific direct-compression process.
Abstract: The present invention relates to Escitalopram having a small median particle size and a solid pharmaceutical composition comprising the same.
Type:
Grant
Filed:
October 18, 2007
Date of Patent:
August 28, 2012
Assignee:
Ratiopharm GmbH
Inventors:
Parshwakumar V. Kalyankar, Ganesh V. Gat, Jawed Hussain
Abstract: The present invention relates to an orally disintegrating dosage form containing aripiprazole. The formulation of the invention shows a fast disintegration.
Type:
Application
Filed:
September 9, 2010
Publication date:
August 23, 2012
Applicant:
ratiopharm GmbH
Inventors:
Parshwakumar V. Kalyankar, Ganesh V. Gat, Javed Hussain
Abstract: The present invention relates to a pharmaceutical composition that comprises the active substance metformin in combination with one of the active substances sitagliptin or vildagliptin. The present invention further relates to a method of production of said pharmaceutical composition.
Abstract: The invention relates to a co-precipitate comprising a phosphodiesterase-5 inhibitor (PDE-5-inhibitor) and a pharmaceutically compatible copolymer carrier comprising 2 or more different acrylic acid derivatives, a method for production thereof and a medication comprising the co-precipitate according to the invention, a method for producing said medication and the use of said medication for treating an illness wherein the inhibiting of phosphodiesterase-5 is of therapeutic benefit.
Abstract: The invention relates to a process for producing pharmaceutically acceptable salts of fingolimod (I), comprising the step of reacting N-[1,1-bis hydroxymethyl-3-(4-octyl phenyl)-propyl]-acylamide (II) with an acidic compound. Furthermore, the invention provides different pharmaceutically acceptable salts of fingolimod and a polymorphic form of fingolimod hydrochloride.
Abstract: The invention concerns desfesoterodine in the form of a tartaric acid salt, in particular in the polymorphic “R form”, as well as a process for its production. In a second aspect, the invention concerns the desfesoterodine of the invention in a microencapsulated form.
Type:
Application
Filed:
May 10, 2010
Publication date:
May 24, 2012
Applicant:
RATIOPHARM GMBH
Inventors:
Dirk Fischer, Gettraud Koellner, Katrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The invention relates to dry processes for the production of oral dosage forms, especially tablets, containing retigabine and adhesion promoter. In addition, the invention relates to compacted intermediates containing retigabine and an adhesion promoter. Finally, the invention relates to single-dose and multiple-dose containers, preferably sachets and stick-packs, containing the intermediate of the invention.
Abstract: The present invention relates to a process for the production of statins, which are known as HMG-CoA reductase inhibitors. A few of the intermediate compounds for use in the process in accordance with the invention are novel compounds and the invention also relates to these novel intermediate compounds.
Type:
Grant
Filed:
April 28, 2006
Date of Patent:
April 3, 2012
Assignee:
Ratiopharm GmbH
Inventors:
Vitali Tararov, Armin Boerner, Gerd Koenig, Andrei Korostylev
Abstract: The invention relates to novel salts of the active substance rasagiline. The salts show excellent processability even after prolonged storage and an excellent storage stability usually superior to known salts after being processed into tablets.
Abstract: The invention relates to an orodispersible tablet comprising the components pharmaceutically acceptable sildenafil salt (a), polymeric adsorbent (b), in particular cation exchanger resin, sweetener (c), and flavoring (d) and, preferably, mucilage (e) and glidant (f).
Abstract: The invention relates to tablets, especially tablets with modified release, containing (a) retigabine and a combination of (b) water-soluble excipient and (c) non-water-soluble excipient; and a process for producing them.
Abstract: The invention relates to solid retigabine in non-crystalline form together with a surface stabiliser in the form of a stable intermediate. In the intermediate of the invention, retigabine is preferably present in amorphous form or in the form of a solid solution. The invention further relates to processes for the production of retigabine in a solid, non-crystalline form and to pharmaceutical formulations containing solid, non-crystalline retigabine.
Abstract: The invention relates to amorphous ambrisentan, preferably together with a surface stabiliser in the form of a stable intermediate. The invention further relates to methods of producing stable amorphous ambrisentan and pharmaceutical formulations containing stable amorphous ambrisentan.
Type:
Application
Filed:
August 7, 2009
Publication date:
January 26, 2012
Applicant:
Ratiopharm GmbH
Inventors:
Kathrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The present invention relates to a pharmaceutical composition comprising N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine as active pharmaceutical ingredient and a process of preparing such composition.
Type:
Application
Filed:
August 24, 2009
Publication date:
January 19, 2012
Applicant:
Ratiopharm GmbH
Inventors:
Katrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The invention relates to an intermediate, obtainable by jointly compacting (i) crystalline cinacalcet or a pharmaceutically acceptable salt thereof, with (ii) a hydrophilising agent, and also tablets containing the intermediates of the invention. The invention further relates to cinacalcet tablets with a bimodal pore size distribution and a method of preparing the tablets of the invention. Finally, the invention relates to the use of a pH adjuster for preparing cinacalcet formulations which can preferably be administered independently of mealtimes.
Type:
Application
Filed:
September 24, 2009
Publication date:
January 12, 2012
Applicant:
RATIOPHARM GMBH
Inventors:
Kathrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The present invention relates to a solid composition containing at least one pharmaceutically compatible auxiliary ingredient and rasagiline or a pharmaceutically compatible salt thereof as an active ingredient. The invention further relates to a method for producing said solid composition and to a medicine comprising said solid composition.
Type:
Application
Filed:
December 18, 2009
Publication date:
December 22, 2011
Applicant:
Ratiopharm GMBH
Inventors:
Katrin Rimkus, Sandra Brueck, Frank Muskulus, Jana Paetz
Abstract: The present invention relates to a pharmaceutical composition comprising N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine as active pharmaceutical ingredient and a process of preparing such composition.
Type:
Application
Filed:
August 24, 2009
Publication date:
December 15, 2011
Applicant:
ratiopharm GmbH
Inventors:
Katrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The invention relates to pharmaceutical compositions comprising 5-Chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)-phenyl]-1,3-oxazolidin-5-yl}-methyl)-2-thiophencarboxamid and processes of preparing such compositions. In a second aspect, the present invention relates to a preferred pellet-layering process for preparing such compositions.
Type:
Application
Filed:
July 7, 2009
Publication date:
December 8, 2011
Applicant:
RATIOPHARM GMBH
Inventors:
Katrin Rimkus, Frank Muskulus, Sandra Brueck, Jana Paetz
Abstract: The invention relates to a process for the preparation of tablets containing moxifloxacin, comprising the steps of (i) providing moxifloxacin, pharmaceutically acceptable salts, solvates or hydrates thereof, optionally mixed with one or more pharmaceutical excipients; (ii) compacting it into a slug; (iii) granulating the slug; and (iv) compressing the resulting granules into tablets; and also tablets, granules and compacted material containing compacted moxifloxacin.