- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07284901
Effekt og sikkerhet ved KAI-9531 administrert én gang i uken hos deltakere med fedme eller overvekt og diabetes (KaiNETIC-2)
En fase 3, randomisert, dobbeltblind, placebokontrollert studie for å evaluere effektiviteten og sikkerheten til KAI-9531 gitt en gang per uke til deltakere med fedme eller overvekt og diabetes
The primary objective of this study is to demonstrate that ribupatide (KAI-9531) subcutaneous (SC) injection once weekly is superior to placebo on:
- Percent change in body weight
- Change in hemoglobin A1c (HbA1c)
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Fase 3
Kontakter og plasseringer
Studiesteder
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-
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Buenos Aires, Argentina, 1056
- Kailera Clinical Site #1
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Buenos Aires, Argentina, 1056
- Kailera Clinical Site #2
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Buenos Aires, Argentina, 1060
- Kailera Clinical Site
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Buenos Aires, Argentina, 1061
- Kailera Clinical Site
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Buenos Aires, Argentina, 1128
- Kailera Clinical Site
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Córdoba, Argentina, 5000
- Kailera Clinical Site
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Córdoba, Argentina, 5002
- Kailera Clinical Site
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Buenos Aires
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Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina, 1120
- Kailera Clinical Site
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La Plata, Buenos Aires, Argentina, 1900
- Kailera Clinical Site
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Mar del Plata, Buenos Aires, Argentina, 7600
- Kailera Clinical Site
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San Nicolás de los Arroyos, Buenos Aires, Argentina, 2900
- Kailera Clinical Site
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Zárate, Buenos Aires, Argentina, 2800
- Kailera Clinical Site
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Mendoza Province
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Godoy Cruz, Mendoza Province, Argentina, 5501
- Kailera Clinical Site
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Santa Fe Province
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Rosario, Santa Fe Province, Argentina, 2000
- Kailera Clinical Site #1
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Rosario, Santa Fe Province, Argentina, 2000
- Kailera Clinical Site #2
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Rosario, Santa Fe Province, Argentina, 2000
- Kailera Clinical Site #3
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Sante Fe
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Rosario, Sante Fe, Argentina, 2000
- Kailera Clinical Site #4
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South Brisbane, Australia, 4101
- Kailera Clinical Site
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Australian Capital Territory
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Bruce, Australian Capital Territory, Australia, 2617
- Kailera Clinical Site
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New South Wales
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Blacktown, New South Wales, Australia, 2148
- Kailera Clinical Site
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Charlestown, New South Wales, Australia, 2290
- Kailera Clinical Site
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Kanwal, New South Wales, Australia, 2259
- Kailera Clinical Site
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Leichhardt, New South Wales, Australia, 2040
- Kailera Clinical Site
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Penrith, New South Wales, Australia, 2750
- Kailera Clinical Site
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Sydney, New South Wales, Australia, 2100
- Kailera Clinical Site
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Sydney, New South Wales, Australia, 2228
- Kailera Clinical Site
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Wollongong, New South Wales, Australia, 2500
- Kailera Clinical Site
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Queensland
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Herston, Queensland, Australia, 4006
- Kailera Clinical Site
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Morayfield, Queensland, Australia, 4506
- Kailera Clinical Site
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Victoria
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Camberwell, Victoria, Australia, 3124
- Kailera Clinical Site
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Melbourne, Victoria, Australia, 3025
- Kailera Clinical Site
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Montana, Bulgaria, 3400
- Kailera Clinical Site
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Kyustendil Province
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Kyustendil, Kyustendil Province, Bulgaria, 2500
- Kailera Clinical Site
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Pleven Province
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Pleven, Pleven Province, Bulgaria, 5800
- Kailera Clinical Site
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Plovdiv Province
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Plovdiv, Plovdiv Province, Bulgaria, 4020
- Kailera Clinical Site
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Ruse Province
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Rousse, Ruse Province, Bulgaria, 7013
- Kailera Clinical Site
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Sofia
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Sofia, Sofia, Bulgaria, 1527
- Kailera Clinical Site
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Sofia, Sofia, Bulgaria, 1606
- Kailera Clinical Site
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Sofia, Sofia, Bulgaria, 1618
- Kailera Clinical Site
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Stara Zagora Province
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Stara Zagora, Stara Zagora Province, Bulgaria, 6000
- Kailera Clinical Site
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Varna Province
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Varna, Varna Province, Bulgaria, 9000
- Kailera Clinical Site
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Alabama
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Cullman, Alabama, Forente stater, 35055
- Kailera Clinical Site
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Arizona
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Phoenix, Arizona, Forente stater, 85012
- Kailera Clinical Site
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Sun City, Arizona, Forente stater, 85351
- Kailera Clinical Site
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Arkansas
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Little Rock, Arkansas, Forente stater, 72205
- Kailera Clinical Site
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California
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Escondido, California, Forente stater, 92025
- Kailera Clinical Site
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La Mesa, California, Forente stater, 91942
- Kailera Clinical Site
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Montclair, California, Forente stater, 91763
- Kailera Clinical Site
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Northridge, California, Forente stater, 91325
- Kailera Clinical Site
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Oceanside, California, Forente stater, 92058
- Kailera Clinical Site
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Toluca Lake, California, Forente stater, 91602
- Kailera Clinical Site
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Connecticut
-
Stamford, Connecticut, Forente stater, 06905
- Kailera Clinical Site
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Florida
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Bradenton, Florida, Forente stater, 34209
- Kailera Clinical Site
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Hollywood, Florida, Forente stater, 33024
- Kailera Clinical Site
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Jupiter, Florida, Forente stater, 33458
- Kailera Clinical Site
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Miami, Florida, Forente stater, 33135
- Kailera Clinical Site
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Miami Lakes, Florida, Forente stater, 33016
- Kailera Clinical Site
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Orange City, Florida, Forente stater, 32763
- Kailera Clinical Site
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Orlando, Florida, Forente stater, 32801
- Kailera Clinical Site
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Orlando, Florida, Forente stater, 32803
- Kailera Clinical Site
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The Villages, Florida, Forente stater, 32162
- Kailera Clinical Site
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Georgia
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Decatur, Georgia, Forente stater, 30030
- Kailera Clinical Site
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Lilburn, Georgia, Forente stater, 30047
- Kailera Clinical Site
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Marietta, Georgia, Forente stater, 30060
- Kailera Clinical Site
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Riverdale, Georgia, Forente stater, 30274
- Kailera Clinical Site
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Illinois
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Skokie, Illinois, Forente stater, 60077
- Kailera Clinical Site
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Springfield, Illinois, Forente stater, 62702
- Kailera Clinical Site
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Kansas
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Newton, Kansas, Forente stater, 67114
- Kailera Clinical Site
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Louisiana
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Shreveport, Louisiana, Forente stater, 71105
- Kailera Clinical Site
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Maryland
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Annapolis, Maryland, Forente stater, 21401
- Kailera Clinical Site
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Columbia, Maryland, Forente stater, 21045
- Kailera Clinical Site
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Massachusetts
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Boston, Massachusetts, Forente stater, 02115
- Kailera Clinical Site
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Michigan
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Farmington Hills, Michigan, Forente stater, 48334
- Kailera Clinical Site
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Montana
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Missoula, Montana, Forente stater, 59804
- Kailera Clinical Site
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Nebraska
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Lincoln, Nebraska, Forente stater, 68516
- Kailera Clinical Site
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Nevada
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Las Vegas, Nevada, Forente stater, 89148
- Kailera Clinical Site
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New York
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Albany, New York, Forente stater, 12203
- Kailera Clinical Site
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Laurelton, New York, Forente stater, 11413
- Kailera Clinical Site
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New York, New York, Forente stater, 10016
- Kailera Clinical Site
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North Carolina
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Greensboro, North Carolina, Forente stater, 27405
- Kailera Clinical Site
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Monroe, North Carolina, Forente stater, 28112
- Kailera Clinical Site
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Morehead City, North Carolina, Forente stater, 28557
- Kailera Clinical Site #1
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Morehead City, North Carolina, Forente stater, 28557
- Kailera Clinical Site #2
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Morrisville, North Carolina, Forente stater, 27560
- Kailera Clinical Site
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Ohio
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Cleveland, Ohio, Forente stater, 44122
- Kailera Clinical Site
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Oklahoma
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Chickasha, Oklahoma, Forente stater, 73018
- Kailera Clinical Site
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Rhode Island
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East Greenwich, Rhode Island, Forente stater, 02818
- Kailera Clinical Site
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South Carolina
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Spartanburg, South Carolina, Forente stater, 29303
- Kailera Clinical Site
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Tennessee
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Chattanooga, Tennessee, Forente stater, 37405
- Kailera Clinical Site
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Memphis, Tennessee, Forente stater, 38119
- Kailera Clinical Site
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Texas
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Amarillo, Texas, Forente stater, 79124
- Kailera Clinical Site
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Brownsville, Texas, Forente stater, 78526
- Kailera Clinical Site
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DeSoto, Texas, Forente stater, 75115
- Kailera Clinical Site
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El Paso, Texas, Forente stater, 79902
- Kailera Clinical Site
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Farmers Branch, Texas, Forente stater, 75234
- Kailera Clinical Site
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Kingwood, Texas, Forente stater, 77345
- Kailera Clinical Site
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Plano, Texas, Forente stater, 75093
- Kailera Clinical Site
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Tomball, Texas, Forente stater, 77375
- Kailera Clinical Site
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Utah
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Pleasant View, Utah, Forente stater, 84404
- Kailera Clinical Site
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Salt Lake City, Utah, Forente stater, 84117
- Kailera Clinical Site
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Virginia
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Manassas, Virginia, Forente stater, 20110
- Kailera Clinical Site
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Richmond, Virginia, Forente stater, 23236
- Kailera Clinical Site
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Washington
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Seattle, Washington, Forente stater, 98104
- Kailera Clinical Site
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Auckland, New Zealand, 1023
- Kailera Clinical Site
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Hastings, New Zealand, 4120
- Kailera Clinical Site
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Nelson, New Zealand, 7011
- Kailera Clinical Site
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Auckland
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Grafton, Auckland, New Zealand, 1010
- Kailera Clinical Site
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New Lynn, Auckland, New Zealand, 0610
- Kailera Clinical Site
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Silverdale, Auckland, New Zealand, 0932
- Kailera Clinical Site
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Takapuna, Auckland, New Zealand, 0622
- Kailera Clinical Site
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Hamilton
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Nawton, Hamilton, New Zealand, 3200
- Kailera Clinical Site
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Krakow, Polen, 30-363
- Kailera Clinical Site
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Warsaw, Polen, 02-677
- Kailera Clinical Site
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Kuyavian-Pomeranian Voivodeship
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Bydgoszcz, Kuyavian-Pomeranian Voivodeship, Polen, 85-231
- Kailera Clinical Site
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Torun, Kuyavian-Pomeranian Voivodeship, Polen, 87-100
- Kailera Clinical Site
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Lesser Poland Voivodeship
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Krakow, Lesser Poland Voivodeship, Polen, 30-033
- Kailera Clinical Site
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Lublin Voivodeship
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Lublin, Lublin Voivodeship, Polen, 20-718
- Kailera Clinical Site
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Masovian Voivodeship
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Siedlce, Masovian Voivodeship, Polen, 08-110
- Kailera Clinical Site
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Warsaw, Masovian Voivodeship, Polen, 00-872
- Kailera Clinical Site
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Podlaskie Voivodeship
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Bialystok, Podlaskie Voivodeship, Polen, 15-351
- Kailera Clinical Site
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Pomeranian Voivodeship
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Gdynia, Pomeranian Voivodeship, Polen, 81-338
- Kailera Clinical Site #1
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Gdynia, Pomeranian Voivodeship, Polen, 81-338
- Kailera Clinical Site #2
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Silesian Voivodeship
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Chorzów, Silesian Voivodeship, Polen, 41-500
- Kailera Clinical Site
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Łódź Voivodeship
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Skierniewice, Łódź Voivodeship, Polen, 96-100
- Kailera Clinical Site
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Świętokrzyskie Voivodeship
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Kielce, Świętokrzyskie Voivodeship, Polen, 25-338
- Kailera Clinical Site
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Bayamón, Puerto Rico, 00959
- Kailera Clinical Site #1
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Bayamón, Puerto Rico, 00959
- Kailera Clinical Site #2
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Ponce, Puerto Rico, 00716
- Kailera Clinical Site
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San Juan, Puerto Rico, 00907
- Kailera Clinical Site
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San Juan, Puerto Rico, 00909
- Kailera Clinical Site
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Vega Baja, Puerto Rico, 693
- Kailera Clinical Site
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Madrid, Spania, 28003
- Kailera Clinical Site
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Seville, Spania, 41003
- Kailera Clinical Site
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Seville, Spania, 41013
- Kailera Clinical Site
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Valencia, Spania, 46014
- Kailera Clinical Site
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A Coruna
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Ferrol, A Coruna, Spania, 15402
- Kailera Clinical Site
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Andalusia
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Seville, Andalusia, Spania, 41010
- Kailera Clinical Site
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Cadiz
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Villamartín, Cadiz, Spania, 11650
- Kailera Clinical Site
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Catalonia
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Barcelona, Catalonia, Spania, 08035
- Kailera Clinical Site
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Principality of Asturias
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Oviedo, Principality of Asturias, Spania, 33011
- Kailera Clinical Site
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Sevilla
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Castilleja de la Cuesta, Sevilla, Spania, 41950
- Kailera Clinical Site
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Manchester, Storbritannia, M13 9WL
- Kailera Clinical Site
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Cornwall
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Truro, Cornwall, Storbritannia, TR1 3LJ
- Kailera Clinical Site
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Devon
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Plymouth, Devon, Storbritannia, PL6 8DH
- Kailera Clinical Site
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Dorset
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Bournemouth, Dorset, Storbritannia, BH7 7DW
- Kailera Clinical Site
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East Yorkshire
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Hull, East Yorkshire, Storbritannia, HU3 2JZ
- Kailera Clinical Site
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Glasgow City
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Glasgow, Glasgow City, Storbritannia, G51 4TF
- Kailera Clinical Site
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Greater London
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London, Greater London, Storbritannia, EC1M 6BQ
- Kailera Clinical Site
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Hertfordshire
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Stevenage, Hertfordshire, Storbritannia, SG1 4AB
- Kailera Clinical Site
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Leicestershire
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Leicester, Leicestershire, Storbritannia, LE5 4PW
- Kailera Clinical Site
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Nottinghamshire
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Nottingham, Nottinghamshire, Storbritannia, NG7 2QW
- Kailera Clinical Site
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South Gloucestershire
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Yate, South Gloucestershire, Storbritannia, BS37 4AX
- Kailera Clinical Site
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Tyne and Wear
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Newcastle upon Tyne, Tyne and Wear, Storbritannia, NE1 4LP
- Kailera Clinical Site
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West Yorkshire
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Bradford, West Yorkshire, Storbritannia, BD9 6RJ
- Kailera Clinical Site
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Hodonín, Tsjekkia, 69501
- Kailera Clinical Site
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Olomouc, Tsjekkia, 77900
- Kailera Clinical Site
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Pardubice, Tsjekkia, 53002
- Kailera Clinical Site
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Prague, Tsjekkia, 15000
- Kailera Clinical Site
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Uherské Hradiště, Tsjekkia, 68601
- Kailera Clinical Site
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Central Bohemia
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Brandýs nad Labem, Central Bohemia, Tsjekkia, 25001
- Kailera Clinical Site
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Hradec Králové Region
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Náchod, Hradec Králové Region, Tsjekkia, 54701
- Kailera Clinical Site
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Trutnov, Hradec Králové Region, Tsjekkia, 54101
- Kailera Clinical Site
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Prague
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Bohnice, Prague, Tsjekkia, 18100
- Kailera Clinical Site
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Prague, Prague, Tsjekkia, 14059
- Kailera Clinical Site
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South Moravian
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Brno, South Moravian, Tsjekkia, 60200
- Kailera Clinical Site
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Zlín
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Holešov, Zlín, Tsjekkia, 76901
- Kailera Clinical Site
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Schwerin, Tyskland, 19055
- Kailera Clinical Site
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Baden-Wurttemberg
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Tübingen, Baden-Wurttemberg, Tyskland, 72076
- Kailera Clinical Site
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Brandenburg
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Falkensee, Brandenburg, Tyskland, 14612
- Kailera Clinical Site
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North Rhine-Westphalia
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Cologne, North Rhine-Westphalia, Tyskland, 51069
- Kailera Clinical Site
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Essen, North Rhine-Westphalia, Tyskland, 45355
- Kailera Clinical Site #1
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Essen, North Rhine-Westphalia, Tyskland, 45355
- Kailera Clinical Site #2
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Schleswig-Holstein
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Oldenburg in Holstein, Schleswig-Holstein, Tyskland, 23758
- Kailera Clinical Site
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Key Inclusion Criteria:
- Diagnosis of type 2 diabetes mellitus (T2DM).
- Receiving stable therapy for T2DM for 3 months prior to Screening. This includes diet and/or exercise alone or in combination with any oral medication for T2DM treatment except for DPP-4 inhibitors. Participants can be treatment naïve if they have an HbA1c of 6.5% to 7.5%, inclusive.
- BMI ≥27 kg/m^2.
- History of being unresponsive to at least 1 self-reported effort to lose weight with diet and/or exercise in the last 6 months.
Key Exclusion Criteria:
- Current diagnosis or history of type 1 diabetes mellitus (T1DM) or any other type of diabetes except T2DM.
- History of diabetic ketoacidosis or hyperosmolar state/coma within 1 year prior to Screening.
- History of severe hypoglycemia or hypoglycemia unawareness within 1 year prior to Screening.
- Started medications within 3 months prior to Screening that may cause significant weight change, including, but not limited to, tricyclic antidepressants, atypical antipsychotics, mood stabilizers, or phentermine.
- Unstable weight defined as self-reported change in body weight exceeding 5% within 3 months prior to Screening.
- Family or personal history of multiple endocrine neoplasia Type 2 or medullary thyroid cancer.
- Uncontrolled hypertension or unstable cardiovascular disease.
- History of chronic or acute pancreatitis.
- Known clinically significant gastric emptying abnormality or chronic treatment with medications that directly affect gastrointestinal (GI) motility if taken for >30 days continually within 3 months prior to Screening.
- History of suicide attempt.
- History of significant active or unstable Major Depressive Disorder (MDD) or other severe psychiatric disorder within 2 years prior to Screening.
- Received treatment with semaglutide, tirzepatide, GLP-1 receptor agonists, GLP-1/glucose-dependent insulinotropic polypeptide (GIP) agonists, glucagon receptor agonists, or other weight loss medications or treatments aside from diet and exercise within 3 months prior to Screening.
Note: Additional inclusion/exclusion criteria may apply, per protocol.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Ribupatide: Dose 1
Participants will receive Dose 1 of ribupatide once weekly. |
SC Injection
Andre navn:
|
|
Eksperimentell: Ribupatide: Dose 2
Participants will receive Dose 2 of ribupatide once weekly. |
SC Injection
Andre navn:
|
|
Eksperimentell: Ribupatide: Dose 3
Participants will receive Dose 3 of ribupatide once weekly. |
SC Injection
Andre navn:
|
|
Eksperimentell: Ribupatide: Dose 4
Participants will receive Dose 4 of ribupatide once weekly. |
SC Injection
Andre navn:
|
|
Placebo komparator: Placebo
Participants will receive placebo matched to ribupatide once weekly. |
SC Injection |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Doses 3 and 4 of Ribupatide Versus Placebo: Percent Change From Baseline in Body Weight at Week 76
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
|
Doses 3 and 4 of Ribupatide Versus Placebo: Change From Baseline in HbA1c at Week 76
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Endring fra baseline i midjeomkrets
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Endring fra baseline i absolutt kroppsvekt
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Endring fra utgangspunkt i systolisk blodtrykk (SBP)
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentvis endring fra utgangspunkt i faste triglyserider
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentvis endring fra baseline i fastende høyttetthetslipoprotein (HDL)-kolesterol
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentvis endring fra baseline for fastende ikke-HDL-kolesterol
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra utgangspunkt i påvirkning av vekt på livskvalitet – Lite klinisk studie-versjon (IWQOL-Lite-CT) fysisk funksjons sammensatt poengsum
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentandel av deltakere med ≥30 % reduksjon i kroppsvekt
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i Control of Eating Questionnaire (CoEQ) Craving Control Score
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra utgangspunkt i CoEQ positiv stemningsscore
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i CoEQ-søtsug score
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i CoEQ craving for salt mat score
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra utgangspunkt i CoEQ Sult-score
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i CoEQ metthetsgrad poengsum
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i CoEQ-kombinert poengsum
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i Food Noise Questionnaire (FNQ)-skår
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Antall deltakere med behandlingsrelaterte bivirkninger (TEAE-er)
Tidsramme: Dag 1 til uke 80
|
Dag 1 til uke 80
|
|
Antall deltakere med legemiddel-antistoffer (ADAer)
Tidsramme: Opp til uke 80
|
Opp til uke 80
|
|
Antall deltakere med nøytraliserende antistoffer (NAbs)
Tidsramme: Opp til uke 80
|
Opp til uke 80
|
|
Prosentandel av deltakere med ≥5 %, ≥10 %, ≥15 %, ≥20 % og ≥25 % reduksjon i kroppsvekt
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra utgangspunkt i fastende blodsukker
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Deltakere med kroppsmasseindeks (KMI) ≥35 kilogram per kvadratmeter (kg/m²): Prosentvis endring fra utgangspunkt i kroppsvekt
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i BMI
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Prosentandel av deltakere med HbA1c <5,7%
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Endring fra baseline i diastolisk blodtrykk (DBP)
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentvis endring fra baseline i faste totalt kolesterol
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Prosentvis endring fra baseline for faste lavtetthetslipoprotein (LDL)-kolesterol
Tidsramme: Baseline, uke 76
|
Baseline, uke 76
|
|
Prosentvis endring fra baseline i veldig lavtetthetslipoprotein (VLDL)-kolesterol
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Prosentvis endring fra baseline for fasteinsulin
Tidsramme: Utgangspunkt, uke 76
|
Utgangspunkt, uke 76
|
|
Doses 1 and 2 of Ribupatide Versus Placebo: Percent Change From Baseline in Body Weight at Week 76
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
|
Doses 1 and 2 of Ribupatide Versus Placebo: Change From Baseline in HbA1c at Week 76
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
|
Percentage of Participants with HbA1c <7% and ≤6.5%
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
|
Plasma Concentrations of Ribupatide
Tidsramme: Up to Week 76
|
Up to Week 76
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studieleder: Medical Director, Kailera Therapeutics, Inc.
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- K9531-3104
- 2025-523510-87-00 (Ctis)
- 2025 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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