Abstract: A recombinant DNA expression vector comprising an Epstein-Barr virus origin of replication, an EBNA-1 gene, a selectable marker expression cassette and a human gamma interferon expression cassette comprising a promoter region, an open reading frame encoding human gamma interferon and a polyadenylation region; a mammalian host cell transformed by said vector; and a process for producing human gamma interferon using said transformed mammalian host cell.
Type:
Grant
Filed:
February 18, 1987
Date of Patent:
July 3, 1990
Assignee:
Meloy Laboratories Inc.
Inventors:
Janet M. Young, Nava Sarver, William N. Drohan
Abstract: Certain specific substituted 9-N-(1-azabicycolo-[2.2.2.]octan-3-yl)carboxamido-2,3,4,5-tetrahydro-1-ben zoxepins and their valuable use as 5-HT.sub.3 antagonists having CNS and gastric prokinetic activity and void of any significant D.sub.2 receptor binding properties are disclosed. Methods for their preparation also are described.
Type:
Grant
Filed:
July 31, 1989
Date of Patent:
May 8, 1990
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Raymond Youssefyeh, Scott I. Klein, Henry F. Campbell, Donald E. Kuhla
Abstract: This invention relates to substituted pyridooxazinone and naphtheridone pyridazinone and pyrazolone compounds which are useful as cardiotonic agents for the treatment of congestive heart failure, to methods for increasing cardiac contractility using said compounds, and pharmaceutical compositions including the same.
Type:
Grant
Filed:
October 11, 1988
Date of Patent:
March 6, 1990
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Alfred P. Spada, William L. Studt, Henry F. Campbell, Donald E. Kuhla, Thomas Tucker
Abstract: A method for increasing cardiotonic contractility in humans or other animals using a class of benzodiazinone-pyridazinone and hydroxy-pyrazolyl compounds and pharmaceutical compositions including the same.
Type:
Grant
Filed:
October 11, 1988
Date of Patent:
March 6, 1990
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
William L. Studt, William C. Faith, Bruce F. Molino
Abstract: Cardiotonic fused aromatic bicyclic ring substituted thiazole compounds and their salts, methods for increasing cardiac contractility in humans and other mammals by the use of said compounds, pharmaceutical compositions including said compounds and methods for compound preparation.
Type:
Grant
Filed:
July 28, 1986
Date of Patent:
April 4, 1989
Assignee:
Rorer Pharmaceutical Corporaton
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt, Bruce F. Molino
Abstract: A class of 3- and 5-amino thiatriazine compounds exhibiting pharmacological activity, including gastrointestinal anti-ulcerogenic and cytoprotective activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
December 9, 1987
Date of Patent:
March 28, 1989
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt, Stuart A. Dodson, Robert A. Galemmo, Jr., Pamela J. Durham
Abstract: This invention relates to imidazolylphenyl and 1,2,4-triazolylphenyl benzopyridazinone and pyridopyridazinone compounds of the formula ##STR1## wherein A is CH or N and not more than one of W, X, Y and Z is a N atom which possess valuable pharmaceutical preparations, e.g., increasing cardiotonic contractility. Uses of said compounds including methods for increasing cardiac contractility and in the treatment of congestive heart failure, pharmaceutical compositions including the same and methods for the preparation thereof.
Type:
Grant
Filed:
July 22, 1987
Date of Patent:
February 21, 1989
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
William C. Faith, Henry F. Campbell, Donald E. Kuhla, William L. Studt, James L. Barnes
Abstract: An acidic aqueous coating composition comprising dissolved phosphate, dissolved aluminum, dissolved dichromate, inorganic colloidal particles and a water miscible organic component including an effective film-forming amount of a water miscible material comprising an ether of a polypropylene glycol, and preferably including also another glycol material, for example, a mono-ethylene glycol material or a mono-propylene glycol material, for use in forming a glaze coating, or a base coating when said composition includes also a particulate material.
Abstract: A class of benzocyclobutene aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
February 26, 1988
Date of Patent:
November 29, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt
Abstract: Benzodiazinone-pyridazinone and -hydroxypyrazolyl compounds possess cardiotonic activity and are included in therapeutic cardiotonic compositions useful in methods for increasing cardiac contractility and for the treatment of congestive heart failure.
Type:
Grant
Filed:
June 17, 1987
Date of Patent:
November 15, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt, William C. Faith, Bruce F. Molino
Abstract: This invention relates to 6-pyridone-carbostyril compounds, uses of said compounds, including methods for increasing cardiac contractility, pharmaceutical compositions including the same and methods for the preparation thereof.
Type:
Grant
Filed:
June 25, 1986
Date of Patent:
November 15, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Henry F. Campbell, Donald E. Kuhla, Bruce F. Molino, William L. Studt
Abstract: Compounds of the formula ##STR1## wherein: Het is imidazol-1-yl or 1,2,4-triazol-1-yl;py is 2-, 3-, or 4-pyridyl;R and R.sub.2 are H or alkyl;R.sub.1 is H, alkyl or vicinal R.sub.1 groups from a C--C double bond; and x is 0 or 1;or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions including the same for cardiotonic uses and methods of treating congestive heart failure.
Type:
Grant
Filed:
October 23, 1985
Date of Patent:
November 8, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt, William C. Faith
Abstract: A class of bicyclic benzo-oxy heterocyclic ether and thioether compounds exhibiting parmacological activity, including anti-secretory and anti-ulcerogenic activity, pharaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
January 7, 1988
Date of Patent:
October 11, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt, Kent W. Neuenschwander
Abstract: A class of bicyclic benzenoid aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcero-genic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
October 5, 1987
Date of Patent:
May 31, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt
Abstract: A process for the preparation of a viscosity-stable antacid composition containing an alginic acid salt comprising reacting an antacid material with said salt at elevated temperatures to form a reaction product and recovering said reaction product in stabilized form.
Type:
Grant
Filed:
March 7, 1986
Date of Patent:
May 17, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Joseph R. Luber, Kenneth M. Feld, Richard J. Harwood, Wayne M. Grim
Abstract: A class of bicyclic benzenoid aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
July 27, 1987
Date of Patent:
May 17, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt
Abstract: A class of benzocyclobutene aminoalkylene ether and thioether compounds exhibiting pharmacological activity, including anti-secretory and anti-ulcerogenic activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
July 28, 1986
Date of Patent:
May 10, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Donald E. Kuhla, Henry F. Campbell, William L. Studt
Abstract: A class of 3- and 5-amino thiatriazine compounds exhibiting pharmacological activity, including anti-ulcerogenic and gastrointestinal cytoprotective activity, pharmaceutical compositions comprising these compounds, and methods for the treatment of gastrointestinal hyperacidity and ulcerogenic disorders in mammals using said compositions.
Type:
Grant
Filed:
April 27, 1984
Date of Patent:
May 3, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
William L. Studt, Donald E. Kuhla, Henry F. Campbell, Stuart A. Dodson
Abstract: A method for the relief of pruritus comprising the administration of an effective antipruritic amount of a N-(trifluoromethylphenyl)anthranilic acid ester to an afflicted patient.
Type:
Grant
Filed:
March 11, 1986
Date of Patent:
March 29, 1988
Assignee:
Rorer Pharmaceutical Corporation
Inventors:
Robert L. Procaccini, Kim D. Lamon, Nicholas S. Hagen