Abstract: The invention relates to an inhalation powder for treating migraine, containing the CGRP antagonist 1-[N2-[3,5-dibromo-N-[[4-(3,4-dihydro-2(1H)-oxoquinazolin-3-yl)-1-piperidinyl]carbonyl]-D-tyrosyl]-L-lysyl]-4-(4-pyridinyl)-piperazine [BIBN4096] of formula I as the active substance base in the form of spherically nanostructured microparticles, and a process for the manufacture thereof.
Type:
Application
Filed:
February 12, 2003
Publication date:
January 22, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co., KG
Abstract: Crystalline forms of the compounds (R)-2-(4-amidinophenylaminomethyl)-1-methyl-5-[1-(carboxymethylamino)-1-(pyrrolidinocarbonyl)-ethyl]-benzimidazole and the monohydrochloride thereof, processes for the preparation thereof and the use thereof as pharmaceutical compositions.
Type:
Application
Filed:
June 17, 2003
Publication date:
January 15, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Guenter Linz, Peter Sieger, Gunnar Schreiner, Werner Rall, Rolf Schmid
Abstract: A pharmaceutical composition comprising:
Type:
Application
Filed:
March 24, 2003
Publication date:
January 15, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Rolf Banholzer, Helmut Meissner, Gerd Morschhaeuser, Michael P. Pieper, Gerald Pohl, Richard Reichl, Georg Speck, Christopher John Montague Meade, Michel Pairet, Ingo Konetzki
Abstract: The invention relates to a crystalline micronisate of (1&agr;,2&bgr;,4&bgr;,5&agr;,7&bgr;)-7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane-bromide, processes for preparing it and its use for preparing a pharmaceutical composition, particularly for preparing a pharmaceutical composition with an anticholinergic activity.
Type:
Application
Filed:
March 10, 2003
Publication date:
January 1, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Helmut Bender, Hagen Graebner, Konrad Schindler, Michael Trunk, Michael Walz
Abstract: The present invention relates to novel pharmaceutical compositions based on a new anticholinergic 1 and heterocyclic compounds 2, processes for preparing them and their use in the treatment of respiratory complaints.
Type:
Application
Filed:
April 8, 2003
Publication date:
January 1, 2004
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Rolf Banholzer, Helmut Meissner, Gerd Morschhaeuser, Michael P. Pieper, Gerald Pohl, Richard Reichl, Georg Speck, Christopher John Montague Meade, Michel Pairet
Abstract: An inhalation kit comprising: (a) an inhaler displaying a flow resistance of about 0.01 to 0.1 {square root}{square root over (kPa)} min/L; and (b) an inhalable powder comprising tiotropium in admixture with a physiologically acceptable excipient with an average particle size of between 10 to 500 &mgr;m, and a method of administering an inhalable powder containing tiotropium in admixture with a physiologically acceptable excipient with an average particle size of between 10 &mgr;m to 500 &mgr;m, the method comprising actuating an inhaler a flow resistance of about 0.01 to 0.1 {square root}{square root over (kPa)} min/L containing the inhalable powder.
Type:
Application
Filed:
April 4, 2003
Publication date:
December 25, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The present invention relates to a new, essentially four-step process for preparing beta-L-2′-deoxy-thymidine starting from L-arabinose. The process according to the invention is particularly important for mass production of beta-L-2′-deoxy-thymidine.
Type:
Application
Filed:
April 14, 2003
Publication date:
December 25, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Franz Dietrich Klingler, Paul Kreye, Wolfgang Baumgarten
Abstract: The invention relates to a new industrially useable process for preparing tropenol, optionally in the form of the acid addition salts thereof.
Type:
Application
Filed:
May 29, 2003
Publication date:
December 25, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Rolf Banholzer, Gisela Bodenbach, Andreas Mathes, Helmut Meissner, Peter Specht
Abstract: The invention relates to new drug combinations based on sodium channel blockers 1 and fibrinolytics 2, processes for the preparation thereof as well as the use thereof for preparing pharmaceutical compositions for the treatment of ischaemic conditions.
Type:
Application
Filed:
June 12, 2003
Publication date:
December 25, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Hermann Duettmann, Annerose Mauz, Sophie Banzet
Abstract: The present invention relates to substituted piperidines of general formula 1
Type:
Application
Filed:
March 13, 2003
Publication date:
December 25, 2003
Applicant:
Boehringer ingelheim Pharma GmbH & Co.
Inventors:
Rudolf Hurnaus, Klaus Rudolf, Stephan Georg Mueller, Dirk Stenkamp, Philipp Lustenberger, Alexander Dreyer, Kai Gerlach, Marcus Schindler, Kirsten Arndt, Eckhart Bauer
Abstract: The present invention relates to the use of 2-amino-4,5,6,7-tetrahydro-6-propylamino-benzothiazole (pramipexole), the (+)- or (−)-enantiomer thereof or one of the pharmacologically acceptable salts thereof in conjunction with another antidepressant for the improved treatment of depression and depressive states.
Type:
Grant
Filed:
July 6, 2000
Date of Patent:
December 23, 2003
Assignee:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The present invention relates to novel pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors, processes for preparing them and their use in the treatment of respiratory diseases.
Type:
Application
Filed:
April 7, 2003
Publication date:
December 4, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Birgit Jung, Michel Pairet, Michael P. Pieper, Hans Clemens Reiser
Abstract: A pharmaceutical composition comprising:
Type:
Application
Filed:
March 19, 2003
Publication date:
December 4, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Rolf Banholzer, Helmut Meissner, Gerd Morschhaeuser, Michael P. Pieper, Gerald Pohl, Richard Reichl, Georg Speck, Christopher John Montague Meade, Michel Pairet
Abstract: The present invention relates to a new pharmaceutical combination for treating benign prostatic hyperplasia (BPH) or for the long-term prevention of acute urinary retention (AUR).
Type:
Application
Filed:
April 24, 2003
Publication date:
December 4, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The present invention relates to the use of specific EGF-receptor antagonists for preparing a pharmaceutical composition for the prevention and/or treatment of benign prostatic hyperplasia and/or prostatic hypertrophy, a method for the treatment or prevention of benign prostatic hyperplasia/prostatic hypertrophy comprising administering an EGF-receptor antagonist of groups (A), (B) or (C), described herein optionally in combination with known compounds for the treatment of benign prostatic hyperplasia/prostatic hypertrophy, as well as associated pharmaceutical compositions.
Type:
Application
Filed:
May 8, 2003
Publication date:
December 4, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & CO. KG
Inventors:
Thomas Singer, Stefan Platz, Florian Colbatzky
Abstract: The invention relates to the use of LTB4 antagonists for preparing a pharmaceutical composition for the treatment or prevention of respiratory diseases in companion and domesticated animals.
Type:
Application
Filed:
March 24, 2003
Publication date:
December 4, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The invention relates to the use of p38 kinase inhibitors for the preparation of a pharmaceutical composition suitable for inhalation for the treatment of mucus hypersecretion. Furthermore the invention is directed to pharmaceutical compositions suitable for inhalation comprising p38 kinase inhibitors and to methods for the preparation thereof.
Type:
Application
Filed:
March 27, 2003
Publication date:
November 27, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Abstract: The present invention relates to genetically engineered mammalian host cells comprising an enhanced level of active anti-apoptosis genes and methods to generate such host cells. More particularly, the invention pertains to methods which modulate the level of anti-apoptosis active genes within host cells and to host cells showing an enhanced cell viability by delaying/inhibiting programmed cell death naturally occurring in such cells.
Type:
Application
Filed:
March 28, 2003
Publication date:
November 27, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Barbara Enenkel, Heiko Meents, Martin Fussenegger
Abstract: The invention relates to a prodrug that is capable of being converted into a drug by the catalytic action of human fibroblast activation protein (FAP&agr;), said prodrug is chemically stable under physiological conditions and can be used for the manufacture of physically stable aqueous formulations. It has a cleavage site which is recognised by FAP&agr;, and the drug released by the enzymatic activity of FAP&agr; is cytotoxic or cytostatic under physiological conditions.
Type:
Application
Filed:
January 3, 2003
Publication date:
November 13, 2003
Applicant:
Boehringer Ingelheim Pharma GmbH & Co. KG
Inventors:
Stefan Blech, Pilar Garin-Chesa, Martin Lenter, John Edward Park, Stefan Peters, Steffen Breitfelder