- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02706483
Langsigtet sikkerhedsundersøgelse af Plecanatid (IBS-C)
En åben etiket, langsigtet undersøgelse af sikkerhed og tolerabilitet af plecanatid hos patienter med irritabel tyktarm med obstipation (IBS-C)
Studieoversigt
Detaljeret beskrivelse
Dette er et fase 3, multicenter, åbent, langsigtet sikkerheds- og tolerabilitetsstudie af 6 mg daglig dosis plecanatid administreret oralt. Patienter, der fuldfører undersøgelser eller kvalificerede screeningsfejl, hvis berettigelse er bekræftet ved afslutningen af deres deltagelse i de dobbeltblindede plecanatid-undersøgelser SP304203-04 eller SP304203-05, vil blive tilmeldt.
Fra dag 1 vil patienterne tage en (1) plecanatid 6,0 mg tablet i klinikken og derefter hver morgen med ca. 240 ml (8 ounce) væske, med eller uden måltider.
Sikkerheds- og tolerabilitetsvurderinger og patienters selvevaluering af sygdommens sværhedsgrad vil blive udført i henhold til skemaet for vurderinger.
Patienter, som afbrydes tidligt fra undersøgelsen, vil gennemgå et tidligt tilbagetrækningsbesøg (EW) inden for 5 dage efter at have stoppet undersøgelseslægemidlet.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 3
Kontakter og lokationer
Studiesteder
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Alabama
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Athens, Alabama, Forenede Stater
- Synergy Research Site
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Birmingham, Alabama, Forenede Stater
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Dothan, Alabama, Forenede Stater
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Foley, Alabama, Forenede Stater
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Guntersville, Alabama, Forenede Stater
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Huntsville, Alabama, Forenede Stater
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Saraland, Alabama, Forenede Stater
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Arizona
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Chandler, Arizona, Forenede Stater
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Phoenix, Arizona, Forenede Stater
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Surprise, Arizona, Forenede Stater
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Tucson, Arizona, Forenede Stater
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Arkansas
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Conway, Arkansas, Forenede Stater
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Glendale, Arkansas, Forenede Stater
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Little Rock, Arkansas, Forenede Stater
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California
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Artesia, California, Forenede Stater
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Canoga Park, California, Forenede Stater
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Carmichael, California, Forenede Stater
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Chula Vista, California, Forenede Stater
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Corona, California, Forenede Stater
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Costa Mesa, California, Forenede Stater
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El Cajon, California, Forenede Stater
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Encino, California, Forenede Stater
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Foothill Ranch, California, Forenede Stater
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Fountain Valley, California, Forenede Stater
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Garden Grove, California, Forenede Stater
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Huntington Beach, California, Forenede Stater
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La Mesa, California, Forenede Stater
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La Mirada, California, Forenede Stater
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Laguna Hills, California, Forenede Stater
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Lancaster, California, Forenede Stater
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Lomita, California, Forenede Stater
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Long Beach, California, Forenede Stater
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Los Angeles, California, Forenede Stater
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North Hollywood, California, Forenede Stater
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Northridge, California, Forenede Stater
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Orange, California, Forenede Stater
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Placentia, California, Forenede Stater
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Riverside, California, Forenede Stater
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San Bernardino, California, Forenede Stater
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San Diego, California, Forenede Stater
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San Marino, California, Forenede Stater
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Sherman Oaks, California, Forenede Stater
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Thousand Oaks, California, Forenede Stater
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Colorado
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Colorado Springs, Colorado, Forenede Stater
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Denver, Colorado, Forenede Stater
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Lafayette, Colorado, Forenede Stater
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Connecticut
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Bristol, Connecticut, Forenede Stater
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Hamden, Connecticut, Forenede Stater
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Florida
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Atlantis, Florida, Forenede Stater
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Boca Raton, Florida, Forenede Stater
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Boynton Beach, Florida, Forenede Stater
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Bradenton, Florida, Forenede Stater
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Brandon, Florida, Forenede Stater
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Brooksville, Florida, Forenede Stater
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Clearwater, Florida, Forenede Stater
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Cutler Bay, Florida, Forenede Stater
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DeLand, Florida, Forenede Stater
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Fort Lauderdale, Florida, Forenede Stater
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Hialeah, Florida, Forenede Stater
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Homestead, Florida, Forenede Stater
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Inverness, Florida, Forenede Stater
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Jacksonville, Florida, Forenede Stater
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Lauderdale Lakes, Florida, Forenede Stater
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Miami, Florida, Forenede Stater
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Miami Lakes, Florida, Forenede Stater
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Miami Springs, Florida, Forenede Stater
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Naples, Florida, Forenede Stater
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North Miami Beach, Florida, Forenede Stater
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Orange Park, Florida, Forenede Stater
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Orlando, Florida, Forenede Stater
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Ormond Beach, Florida, Forenede Stater
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Oviedo, Florida, Forenede Stater
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Pembroke Pines, Florida, Forenede Stater
- Synergy Research Site
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Pinellas Park, Florida, Forenede Stater
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Port Orange, Florida, Forenede Stater
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Saint Petersburg, Florida, Forenede Stater
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Tamarac, Florida, Forenede Stater
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Tampa, Florida, Forenede Stater
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Georgia
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Atlanta, Georgia, Forenede Stater
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Marietta, Georgia, Forenede Stater
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Snellville, Georgia, Forenede Stater
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Idaho
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Blackfoot, Idaho, Forenede Stater
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Boise, Idaho, Forenede Stater
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Meridian, Idaho, Forenede Stater
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Illinois
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Blue Island, Illinois, Forenede Stater
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Chicago, Illinois, Forenede Stater
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Evanston, Illinois, Forenede Stater
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Evergreen Park, Illinois, Forenede Stater
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Hoffman Estates, Illinois, Forenede Stater
- Synergy Research Site
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Morton, Illinois, Forenede Stater
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Oak Lawn, Illinois, Forenede Stater
- Synergy Research Site
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Schaumburg, Illinois, Forenede Stater
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Indiana
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Brownsburg, Indiana, Forenede Stater
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Indianapolis, Indiana, Forenede Stater
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Kansas
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Topeka, Kansas, Forenede Stater
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Wichita, Kansas, Forenede Stater
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Kentucky
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Madisonville, Kentucky, Forenede Stater
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Owensboro, Kentucky, Forenede Stater
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Louisiana
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Baton Rouge, Louisiana, Forenede Stater
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Crowley, Louisiana, Forenede Stater
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Mandeville, Louisiana, Forenede Stater
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Marrero, Louisiana, Forenede Stater
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Metairie, Louisiana, Forenede Stater
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New Orleans, Louisiana, Forenede Stater
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Shreveport, Louisiana, Forenede Stater
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Maryland
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Annapolis, Maryland, Forenede Stater
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Baltimore, Maryland, Forenede Stater
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Hagerstown, Maryland, Forenede Stater
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Oxon Hill, Maryland, Forenede Stater
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Massachusetts
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Marlborough, Massachusetts, Forenede Stater
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Michigan
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Chesterfield, Michigan, Forenede Stater
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Flint, Michigan, Forenede Stater
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Wyoming, Michigan, Forenede Stater
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Mississippi
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Jackson, Mississippi, Forenede Stater
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Port Gibson, Mississippi, Forenede Stater
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Missouri
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Chesterfield, Missouri, Forenede Stater
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Hazelwood, Missouri, Forenede Stater
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Saint Louis, Missouri, Forenede Stater
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Montana
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Missoula, Montana, Forenede Stater
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Nebraska
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Omaha, Nebraska, Forenede Stater
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New Jersey
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Marlton, New Jersey, Forenede Stater
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New Mexico
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Albuquerque, New Mexico, Forenede Stater
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New York
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Brooklyn, New York, Forenede Stater
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Great Neck, New York, Forenede Stater
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Hopewell Junction, New York, Forenede Stater
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Kew Gardens, New York, Forenede Stater
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New Windsor, New York, Forenede Stater
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New York, New York, Forenede Stater
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North Massapequa, New York, Forenede Stater
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Poughkeepsie, New York, Forenede Stater
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North Carolina
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Asheboro, North Carolina, Forenede Stater
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Cary, North Carolina, Forenede Stater
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Charlotte, North Carolina, Forenede Stater
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Charlotte, North Carolina, Forenede Stater
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Davidson, North Carolina, Forenede Stater
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Fayetteville, North Carolina, Forenede Stater
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High Point, North Carolina, Forenede Stater
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Jacksonville, North Carolina, Forenede Stater
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Kinston, North Carolina, Forenede Stater
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Raleigh, North Carolina, Forenede Stater
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Salisbury, North Carolina, Forenede Stater
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Wilmington, North Carolina, Forenede Stater
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Winston-Salem, North Carolina, Forenede Stater
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North Dakota
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Fargo, North Dakota, Forenede Stater
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Ohio
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Beavercreek, Ohio, Forenede Stater
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Cincinnati, Ohio, Forenede Stater
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Columbus, Ohio, Forenede Stater
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Dayton, Ohio, Forenede Stater
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Englewood, Ohio, Forenede Stater
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Kettering, Ohio, Forenede Stater
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Mentor, Ohio, Forenede Stater
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Middleburg Heights, Ohio, Forenede Stater
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Oklahoma
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Oklahoma City, Oklahoma, Forenede Stater
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Oregon
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Portland, Oregon, Forenede Stater
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Pennsylvania
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Lansdale, Pennsylvania, Forenede Stater
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Levittown, Pennsylvania, Forenede Stater
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Philadelphia, Pennsylvania, Forenede Stater
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Smithfield, Pennsylvania, Forenede Stater
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South Carolina
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Anderson, South Carolina, Forenede Stater
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Gaffney, South Carolina, Forenede Stater
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Greer, South Carolina, Forenede Stater
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South Dakota
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Rapid City, South Dakota, Forenede Stater
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Tennessee
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Athens, Tennessee, Forenede Stater
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Chattanooga, Tennessee, Forenede Stater
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Fayetteville, Tennessee, Forenede Stater
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Franklin, Tennessee, Forenede Stater
- Synergy Research Site
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Hermitage, Tennessee, Forenede Stater
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Jackson, Tennessee, Forenede Stater
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Kingsport, Tennessee, Forenede Stater
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Knoxville, Tennessee, Forenede Stater
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Memphis, Tennessee, Forenede Stater
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Nashville, Tennessee, Forenede Stater
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Texas
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Austin, Texas, Forenede Stater
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Beaumont, Texas, Forenede Stater
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Carrollton, Texas, Forenede Stater
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Channelview, Texas, Forenede Stater
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Dallas, Texas, Forenede Stater
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Houston, Texas, Forenede Stater
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Humble, Texas, Forenede Stater
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Lampasas, Texas, Forenede Stater
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McKinney, Texas, Forenede Stater
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Missouri City, Texas, Forenede Stater
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Plano, Texas, Forenede Stater
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Port Arthur, Texas, Forenede Stater
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San Antonio, Texas, Forenede Stater
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Sugar Land, Texas, Forenede Stater
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Utah
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Ogden, Utah, Forenede Stater
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Orem, Utah, Forenede Stater
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Saint George, Utah, Forenede Stater
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Sandy, Utah, Forenede Stater
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Virginia
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Charlottesville, Virginia, Forenede Stater
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Chesapeake, Virginia, Forenede Stater
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Fairfax, Virginia, Forenede Stater
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Lynchburg, Virginia, Forenede Stater
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Newport News, Virginia, Forenede Stater
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Norfolk, Virginia, Forenede Stater
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Richmond, Virginia, Forenede Stater
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Washington
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Bellevue, Washington, Forenede Stater
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Spokane, Washington, Forenede Stater
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West Virginia
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Charleston, West Virginia, Forenede Stater
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Kingwood, West Virginia, Forenede Stater
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Morgantown, West Virginia, Forenede Stater
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Wisconsin
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La Crosse, Wisconsin, Forenede Stater
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Milwaukee, Wisconsin, Forenede Stater
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inklusionskriterier:
Patienter med dokumenteret diagnose af IBS-C, som:
- Fuldførte plecanatid-undersøgelse SP304203-04 eller SP304203-05, var i overensstemmelse med den tidligere undersøgelses krav og oplevede ikke nogen alvorlig bivirkning (SAE), der anses for at være relateret til undersøgelseslægemidlet i løbet af det forrige studie, ELLER
- Mislykket screening i undersøgelse SP304203-04 eller SP304203-05 på grund af manglende overholdelse af dagbog (en udelukkelse i kerneundersøgelsen) eller på grund af en administrativ årsag og har tilladelse til at deltage i denne undersøgelse ved meddelelse fra sponsor eller delegeret.
Nøgleekskluderingskriterier:
- Patienten er uvillig eller ude af stand til at: deltage i undersøgelsen i den krævede varighed, forstå og underskrive den informerede samtykkeformular (ICF) og gennemgå alle protokolrelaterede tests og procedurer gennem hele undersøgelsen.
- Kvindelig patient i den fødedygtige alder med en positiv uringraviditetstest på dag 1.
- Mandlige og kvindelige patienter i den fødedygtige alder, som ikke er enige om at fortsætte med at bruge den præventionsmetode, der blev brugt i det dobbeltblindede plecanatid-studie i hele dette kliniske forsøg.
- Patienten har oplevet en signifikant negativ ændring i helbredsstatus i løbet af deltagelse i det dobbeltblindede plecanatid-kernestudie eller efter afslutning af undersøgelsen.
- Efter Investigator eller Medical Monitors opfattelse er det ikke i patientens bedste interesse at deltage i undersøgelsen. Årsag(erne) til patientens udelukkelse skal specificeres.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Plecanatid
Plecanatid 6,0 mg tabletter
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Antal deltagere med behandlingsrelaterede bivirkninger.
Tidsramme: op til 53 uger
|
Antal deltagere med uønskede hændelser med evidens, der tyder på en årsagssammenhæng mellem behandling og undersøgelseslægemiddel.
|
op til 53 uger
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i fordøjelsessystemet
- Patologiske processer
- Sygdom
- Gastrointestinale sygdomme
- Tyktarmssygdomme, funktionelle
- Tyktarmssygdomme
- Tarmsygdomme
- Syndrom
- Irritabelt tarmsyndrom
- Molekylære mekanismer for farmakologisk virkning
- Gastrointestinale midler
- Guanylyl Cyclase C agonister
- Enzymaktivatorer
- Plecanatid
Andre undersøgelses-id-numre
- SP304203-06
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Irritabelt tarmsyndrom
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Seoul National University HospitalUkendtSund og rask | Kronisk forstoppelse | Constipated Irritable Bowel Syndrome
-
Hacettepe UniversityAfsluttetKolorektal cancer | Ammende | Koloskopi forberedelse | Boston Bowel Preparation ScaleKalkun
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GlaxoSmithKlineIkke rekrutterer endnu
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Helen Keller Eye Research FoundationFive Lakes Clinical Research Consulting, LLCRekrutteringStickler syndrom type 2 | Stickler syndrom type 1Forenede Stater
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Unravel Biosciences, Inc.RekrutteringPitt Hopkins syndromColombia
-
University of California, Los AngelesBoston Children's Hospital; Duke University; Children's Hospital Medical...RekrutteringBohring-Opitz syndrom | ASXL1 genmutation | Shashi-Pena syndrom | ASXL2-genmutation | Bainbridge-Ropers syndrom | ASXL3 genmutationForenede Stater
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Neuren Pharmaceuticals LimitedRekrutteringPhelan-McDermid syndromForenede Stater
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Neuren Pharmaceuticals LimitedRekrutteringPhelan-McDermid syndromForenede Stater
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University of California, DavisNational Cancer Institute (NCI); Celgene; Pharmacyclics LLC.AfsluttetTidligere behandlet myelodysplastisk syndrom | Myelodysplastisk syndrom | Terapi-relateret myelodysplastisk syndrom | Sekundært myelodysplastisk syndrom | Refraktært højrisiko myelodysplastisk syndromForenede Stater
-
Riphah International UniversityAfsluttet
Kliniske forsøg med Plecanatid
-
Bausch Health Americas, Inc.ParexelAfsluttetKronisk idiopatisk obstipationForenede Stater
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Bausch Health Americas, Inc.AfsluttetKronisk idiopatisk obstipationForenede Stater
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Bausch Health Americas, Inc.AfsluttetKronisk idiopatisk obstipationForenede Stater
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Bausch Health Americas, Inc.Syneos HealthAfsluttetKronisk idiopatisk obstipationForenede Stater, Canada
-
Shandong Luoxin Pharmaceutical Group Stock Co.,...AfsluttetFunktionel forstoppelseKina
-
Bausch Health Americas, Inc.AfsluttetIrritabel tyktarm karakteriseret ved forstoppelseForenede Stater
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Bausch Health Americas, Inc.AfsluttetIrritabel tyktarm karakteriseret ved forstoppelseForenede Stater
-
Bausch Health Americas, Inc.AfsluttetIrritabel tyktarm karakteriseret ved forstoppelseForenede Stater
-
Bausch Health Americas, Inc.AfsluttetIrritabel tyktarm med forstoppelseForenede Stater
-
Bausch Health Americas, Inc.AfsluttetKronisk idiopatisk obstipationForenede Stater