US2016340390A1PendingUtilityA1
Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
Est. expiryJun 4, 2027(~0.9 yrs left)· nominal 20-yr term from priority
A61P 9/04A61P 35/04A61P 3/06A61P 9/12A61P 43/00A61P 35/02A61P 3/10A61P 27/06A61P 35/00A61P 29/00A61P 27/04A61P 13/08A61P 1/04A61P 1/16A61P 17/06A61P 11/06A61P 1/10A61P 1/18A61P 11/16A61P 1/02A61P 1/00A61P 1/14A61P 11/00A61K 38/10A61K 47/02A61K 31/519A61K 47/60A61K 9/02C07K 7/08A61K 9/0031A61K 9/08C07K 7/64A61K 38/12A61K 45/06A61K 31/192
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Claims
Abstract
The invention provides novel guanylate cyclase-C agonist peptides and their use in the treatment of human diseases including gastrointestinal disorders, inflammation or cancer (e.g., a gastrointestinal cancer). The peptides can be administered either alone or in combination with an inhibitor of cGMP-dependent phosphodiesterase. The gastrointestinal disorder may be classified as either irritable bowel syndrome, constipation, or excessive acidity etc. The gastrointestinal disease may be classified as either inflammatory bowel disease or other GI condition, including Crohn's disease and ulcerative colitis, and cancer.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A peptide consisting essentially of the amino acid sequence of SEQ ID NO:16.
2 . A pharmaceutical composition in unit dose form comprising a guanylate cyclase receptor agonist peptide having the sequence of SEQ ID NO:16 present in a therapeutically effective amount and a pharmaceutical carrier, excipient or diluent.
3 . The pharmaceutical composition of claim 2 , wherein the unit dose form is selected from the group consisting of a tablet, a capsule, a solution and inhalation formulation.
4 . A method for preventing or treating a condition selected from the group consisting of Ulcerative Colitis, Irritable bowel syndrome (IBS), non-ulcer dyspepsia chronic intestinal pseudo-obstruction, functional dyspepsia, colonic pseudo-obstruction, duodenogastric reflux, constipation associated with use of opiate pain killers, gastroesophageal reflux disease (GERD), post surgical constipation, gastroparesis, constipation associated with neuropathic disorders, heartburn, poor gastrointestinal motility, congestive heart failure, hypertension, benign prostatic hyperplasia (BPH), colon cancer, lung cancer, bladder cancer, liver cancer, salivary gland cancer or skin cancer, bronchitis, tissue inflammation, organ inflammation, respiratory inflammation, asthma, and COPD comprising administering to a patient in need thereof, an effective dosage of a guanylate cyclase receptor agonist having the sequence of SEQ ID NO:16.
5 . A method of claim 4 , further comprising administering an effective dose of a cGMP-dependent phosphodiesterase inhibitor.
6 . The method of claim 5 , further comprising administering to said patient an effective dose of a cGMP-dependent phosphodiesterase inhibitor either concurrently or sequentially with said guanylate cyclase receptor agonist.
7 . The method of claim 6 , wherein said cGMP-dependent phosphodiesterase inhibitor is selected from the group consisting of sulindac sulfone, zaprinast, motapizone, vardenafil, and sildenafil.
8 . The method of claim 5 , further comprising administering an effective does of at least one anti-inflammatory agent.
9 . The method of claim 8 , wherein said anti-inflammatory agent is a steroid or nonsteroid anti-inflammatory drug (NSAID).
10 . Use of a peptides having the sequence of SEQ ID NO:16 in the manufacture of a medicament for the treatment of a human disease.
11 . A method of increasing cGMP production in a cell comprising contacting said cell with a peptide comprising the amino acid sequence of SEQ ID NO:16.
12 . The method of claim 11 , further comprising contacting said cell with a cGMP-dependent phosphodiesterase inhibitor.
13 . The method of claim 12 , wherein said cGMP-dependent phosphodiesterase inhibitor is selected from the group consisting of sulindac sulfone, zaprinast, motapizone, vardenafil, and sildenafil.Cited by (0)
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