Patents by Inventor Graham Nigel Maw

Graham Nigel Maw has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 6200978
    Abstract: Compounds of the formula (I)—shown below—are described. The compounds are useful in the manufacture of a pharmaceutical composition for preventing or treating inflammatory diseases such as arthritis, psoriasis, asthma, or inflammatory bowel disease, disorders of respiratory function, gastrointestinal disorders such as functional bowel disease, functional GI disorders such as irritable bowel syndrome, functional diarrhoea, functional distension, functional pain, non-ulcerogenic dyspepsia or others associated with disorders of motility or secretion, urogenital tract disorders such as incontinence, as analgesics for treating pain including non-somatic pain, or as immunosuppressants to prevent rejection in organ transplant and skin graft.
    Type: Grant
    Filed: March 3, 1999
    Date of Patent: March 13, 2001
    Assignee: Pfizer Inc.
    Inventors: Graham Nigel Maw, Donald Stuart Middleton
  • Patent number: 5922747
    Abstract: A method of treatment of a human to inhibit a steroid 5.alpha.-reductase, particularly a testosterone 5.alpha.-reductase, which comprises treating said human with an effective amount of a compound of the formula (I) ##STR1## or a pharmaceutically acceptable base salt thereof, wherein R is --CO.sub.2 H or tetrazol-5-yl;R.sup.1 is C.sub.3 -C.sub.8 alkyl optionally substituted by fluoro; andR.sup.2 is C.sub.2 -C.sub.4 alkylor with a pharmaceutically acceptable base salt or composition thereof. Conditions which are treatable by such inhibition include acne vulgaris, alopecia, seborrhoea, female hirsutism, benign prostatic hypertropy, male pattern baldness and human prostate adenocarcinomas.
    Type: Grant
    Filed: December 2, 1997
    Date of Patent: July 13, 1999
    Assignee: Pfizer Inc.
    Inventors: Julian Blagg, Graham Nigel Maw, David James Rawson
  • Patent number: 5912357
    Abstract: A compound of formula (I): ##STR1## and the pharmaceutically acceptable base salts thereof, wherein: R is CO.sub.2 R.sup.12 where R.sup.12 is H or a biolabile ester-forming group, or R is tetrazol-5-yl, and either (a) R.sup.1 is ##STR2## and R.sup.2 is F, Cl, Br, I, CH.sub.3 or CF.sub.3, or (b) R.sup.1 is C.sub.3 -C.sub.6 alkyl and R.sup.2 is C.sub.2 -C.sub.4 alkyl, useful as steroid 5-.alpha.-reductase inhibitors.
    Type: Grant
    Filed: February 15, 1996
    Date of Patent: June 15, 1999
    Assignee: Pfizer Inc
    Inventors: Julian Blagg, Graham Nigel Maw, David James Rawson
  • Patent number: 5767139
    Abstract: The present invention provides compounds of the formula: ##STR1## and the pharmaceutically acceptable salts thereof, together with pharmaceutically compositions containing, uses of, processes for the preparation of and intermediates used in the preparation of, such compounds.
    Type: Grant
    Filed: August 2, 1994
    Date of Patent: June 16, 1998
    Assignee: Pfizer, Inc.
    Inventors: Graham Nigel Maw, Julian Blagg, Colin William Greengrass, Paul William Finn
  • Patent number: 5696146
    Abstract: Compounds of formula (I) ##STR1## and the pharmaceutically acceptable base salts thereof, wherein R is --CO.sub.2 H or tetrazol-5 yl; R.sup.1 is C.sub.3 -C.sub.8 alkyl optionally substituted by fluoro; and R.sup.2 is C.sub.2 -C.sub.4 alkyl, together with compositions containing, uses of, process for the preparation of, and intermediates used in the preparation of, such compounds. The compounds have steroid 5.alpha.-reductase inhibitory activity and are useful for treating a disease such as benign prostatic hypertrophy.
    Type: Grant
    Filed: November 16, 1995
    Date of Patent: December 9, 1997
    Assignee: Pfizer Inc.
    Inventors: Julian Blagg, Graham Nigel Maw, David James Rawson