- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07284901
Effekt og sikkerhed ved KAI-9531 administreret en gang ugentligt hos deltagere med overvægt eller fedme og diabetes (KaiNETIC-2)
En fase 3, randomiseret, dobbeltblind, placebokontrolleret undersøgelse for at vurdere effektiviteten og sikkerheden af KAI-9531 administreret en gang om ugen hos deltagere med fedme eller overvægt 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)
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 3
Kontakter og lokationer
Studiesteder
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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, Australien, 4101
- Kailera Clinical Site
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Australian Capital Territory
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Bruce, Australian Capital Territory, Australien, 2617
- Kailera Clinical Site
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New South Wales
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Blacktown, New South Wales, Australien, 2148
- Kailera Clinical Site
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Charlestown, New South Wales, Australien, 2290
- Kailera Clinical Site
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Kanwal, New South Wales, Australien, 2259
- Kailera Clinical Site
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Leichhardt, New South Wales, Australien, 2040
- Kailera Clinical Site
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Penrith, New South Wales, Australien, 2750
- Kailera Clinical Site
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Sydney, New South Wales, Australien, 2100
- Kailera Clinical Site
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Sydney, New South Wales, Australien, 2228
- Kailera Clinical Site
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Wollongong, New South Wales, Australien, 2500
- Kailera Clinical Site
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Queensland
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Herston, Queensland, Australien, 4006
- Kailera Clinical Site
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Morayfield, Queensland, Australien, 4506
- Kailera Clinical Site
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Victoria
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Camberwell, Victoria, Australien, 3124
- Kailera Clinical Site
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Melbourne, Victoria, Australien, 3025
- Kailera Clinical Site
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Montana, Bulgarien, 3400
- Kailera Clinical Site
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Kyustendil Province
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Kyustendil, Kyustendil Province, Bulgarien, 2500
- Kailera Clinical Site
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Pleven Province
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Pleven, Pleven Province, Bulgarien, 5800
- Kailera Clinical Site
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Plovdiv Province
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Plovdiv, Plovdiv Province, Bulgarien, 4020
- Kailera Clinical Site
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Ruse Province
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Rousse, Ruse Province, Bulgarien, 7013
- Kailera Clinical Site
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Sofia
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Sofia, Sofia, Bulgarien, 1527
- Kailera Clinical Site
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Sofia, Sofia, Bulgarien, 1606
- Kailera Clinical Site
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Sofia, Sofia, Bulgarien, 1618
- Kailera Clinical Site
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Stara Zagora Province
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Stara Zagora, Stara Zagora Province, Bulgarien, 6000
- Kailera Clinical Site
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Varna Province
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Varna, Varna Province, Bulgarien, 9000
- Kailera Clinical Site
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Manchester, Det Forenede Kongerige, M13 9WL
- Kailera Clinical Site
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Cornwall
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Truro, Cornwall, Det Forenede Kongerige, TR1 3LJ
- Kailera Clinical Site
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Devon
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Plymouth, Devon, Det Forenede Kongerige, PL6 8DH
- Kailera Clinical Site
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Dorset
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Bournemouth, Dorset, Det Forenede Kongerige, BH7 7DW
- Kailera Clinical Site
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East Yorkshire
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Hull, East Yorkshire, Det Forenede Kongerige, HU3 2JZ
- Kailera Clinical Site
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Glasgow City
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Glasgow, Glasgow City, Det Forenede Kongerige, G51 4TF
- Kailera Clinical Site
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Greater London
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London, Greater London, Det Forenede Kongerige, EC1M 6BQ
- Kailera Clinical Site
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Hertfordshire
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Stevenage, Hertfordshire, Det Forenede Kongerige, SG1 4AB
- Kailera Clinical Site
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Leicestershire
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Leicester, Leicestershire, Det Forenede Kongerige, LE5 4PW
- Kailera Clinical Site
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Nottinghamshire
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Nottingham, Nottinghamshire, Det Forenede Kongerige, NG7 2QW
- Kailera Clinical Site
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South Gloucestershire
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Yate, South Gloucestershire, Det Forenede Kongerige, BS37 4AX
- Kailera Clinical Site
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Tyne and Wear
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Newcastle upon Tyne, Tyne and Wear, Det Forenede Kongerige, NE1 4LP
- Kailera Clinical Site
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West Yorkshire
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Bradford, West Yorkshire, Det Forenede Kongerige, BD9 6RJ
- Kailera Clinical Site
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Alabama
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Cullman, Alabama, Forenede Stater, 35055
- Kailera Clinical Site
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Arizona
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Phoenix, Arizona, Forenede Stater, 85012
- Kailera Clinical Site
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Sun City, Arizona, Forenede Stater, 85351
- Kailera Clinical Site
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Arkansas
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Little Rock, Arkansas, Forenede Stater, 72205
- Kailera Clinical Site
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California
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Escondido, California, Forenede Stater, 92025
- Kailera Clinical Site
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La Mesa, California, Forenede Stater, 91942
- Kailera Clinical Site
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Montclair, California, Forenede Stater, 91763
- Kailera Clinical Site
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Northridge, California, Forenede Stater, 91325
- Kailera Clinical Site
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Oceanside, California, Forenede Stater, 92058
- Kailera Clinical Site
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Toluca Lake, California, Forenede Stater, 91602
- Kailera Clinical Site
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Connecticut
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Stamford, Connecticut, Forenede Stater, 06905
- Kailera Clinical Site
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Florida
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Bradenton, Florida, Forenede Stater, 34209
- Kailera Clinical Site
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Hollywood, Florida, Forenede Stater, 33024
- Kailera Clinical Site
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Jupiter, Florida, Forenede Stater, 33458
- Kailera Clinical Site
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Miami, Florida, Forenede Stater, 33135
- Kailera Clinical Site
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Miami Lakes, Florida, Forenede Stater, 33016
- Kailera Clinical Site
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Orange City, Florida, Forenede Stater, 32763
- Kailera Clinical Site
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Orlando, Florida, Forenede Stater, 32801
- Kailera Clinical Site
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Orlando, Florida, Forenede Stater, 32803
- Kailera Clinical Site
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The Villages, Florida, Forenede Stater, 32162
- Kailera Clinical Site
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Georgia
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Decatur, Georgia, Forenede Stater, 30030
- Kailera Clinical Site
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Lilburn, Georgia, Forenede Stater, 30047
- Kailera Clinical Site
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Marietta, Georgia, Forenede Stater, 30060
- Kailera Clinical Site
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Riverdale, Georgia, Forenede Stater, 30274
- Kailera Clinical Site
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Illinois
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Skokie, Illinois, Forenede Stater, 60077
- Kailera Clinical Site
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Springfield, Illinois, Forenede Stater, 62702
- Kailera Clinical Site
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Kansas
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Newton, Kansas, Forenede Stater, 67114
- Kailera Clinical Site
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Louisiana
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Shreveport, Louisiana, Forenede Stater, 71105
- Kailera Clinical Site
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Maryland
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Annapolis, Maryland, Forenede Stater, 21401
- Kailera Clinical Site
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Columbia, Maryland, Forenede Stater, 21045
- Kailera Clinical Site
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02115
- Kailera Clinical Site
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Michigan
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Farmington Hills, Michigan, Forenede Stater, 48334
- Kailera Clinical Site
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Montana
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Missoula, Montana, Forenede Stater, 59804
- Kailera Clinical Site
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Nebraska
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Lincoln, Nebraska, Forenede Stater, 68516
- Kailera Clinical Site
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Nevada
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Las Vegas, Nevada, Forenede Stater, 89148
- Kailera Clinical Site
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New York
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Albany, New York, Forenede Stater, 12203
- Kailera Clinical Site
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Laurelton, New York, Forenede Stater, 11413
- Kailera Clinical Site
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New York, New York, Forenede Stater, 10016
- Kailera Clinical Site
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North Carolina
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Greensboro, North Carolina, Forenede Stater, 27405
- Kailera Clinical Site
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Monroe, North Carolina, Forenede Stater, 28112
- Kailera Clinical Site
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Morehead City, North Carolina, Forenede Stater, 28557
- Kailera Clinical Site #1
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Morehead City, North Carolina, Forenede Stater, 28557
- Kailera Clinical Site #2
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Morrisville, North Carolina, Forenede Stater, 27560
- Kailera Clinical Site
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Ohio
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Cleveland, Ohio, Forenede Stater, 44122
- Kailera Clinical Site
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Oklahoma
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Chickasha, Oklahoma, Forenede Stater, 73018
- Kailera Clinical Site
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Rhode Island
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East Greenwich, Rhode Island, Forenede Stater, 02818
- Kailera Clinical Site
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South Carolina
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Spartanburg, South Carolina, Forenede Stater, 29303
- Kailera Clinical Site
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Tennessee
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Chattanooga, Tennessee, Forenede Stater, 37405
- Kailera Clinical Site
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Memphis, Tennessee, Forenede Stater, 38119
- Kailera Clinical Site
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Texas
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Amarillo, Texas, Forenede Stater, 79124
- Kailera Clinical Site
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Brownsville, Texas, Forenede Stater, 78526
- Kailera Clinical Site
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DeSoto, Texas, Forenede Stater, 75115
- Kailera Clinical Site
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El Paso, Texas, Forenede Stater, 79902
- Kailera Clinical Site
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Farmers Branch, Texas, Forenede Stater, 75234
- Kailera Clinical Site
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Kingwood, Texas, Forenede Stater, 77345
- Kailera Clinical Site
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Plano, Texas, Forenede Stater, 75093
- Kailera Clinical Site
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Tomball, Texas, Forenede Stater, 77375
- Kailera Clinical Site
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Utah
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Pleasant View, Utah, Forenede Stater, 84404
- Kailera Clinical Site
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Salt Lake City, Utah, Forenede Stater, 84117
- Kailera Clinical Site
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Virginia
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Manassas, Virginia, Forenede Stater, 20110
- Kailera Clinical Site
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Richmond, Virginia, Forenede Stater, 23236
- Kailera Clinical Site
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Washington
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Seattle, Washington, Forenede 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, Spanien, 28003
- Kailera Clinical Site
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Seville, Spanien, 41003
- Kailera Clinical Site
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Seville, Spanien, 41013
- Kailera Clinical Site
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Valencia, Spanien, 46014
- Kailera Clinical Site
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A Coruna
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Ferrol, A Coruna, Spanien, 15402
- Kailera Clinical Site
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Andalusia
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Seville, Andalusia, Spanien, 41010
- Kailera Clinical Site
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Cadiz
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Villamartín, Cadiz, Spanien, 11650
- Kailera Clinical Site
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Catalonia
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Barcelona, Catalonia, Spanien, 08035
- Kailera Clinical Site
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Principality of Asturias
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Oviedo, Principality of Asturias, Spanien, 33011
- Kailera Clinical Site
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Sevilla
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Castilleja de la Cuesta, Sevilla, Spanien, 41950
- Kailera Clinical Site
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Hodonín, Tjekkiet, 69501
- Kailera Clinical Site
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Olomouc, Tjekkiet, 77900
- Kailera Clinical Site
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Pardubice, Tjekkiet, 53002
- Kailera Clinical Site
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Prague, Tjekkiet, 15000
- Kailera Clinical Site
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Uherské Hradiště, Tjekkiet, 68601
- Kailera Clinical Site
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Central Bohemia
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Brandýs nad Labem, Central Bohemia, Tjekkiet, 25001
- Kailera Clinical Site
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Hradec Králové Region
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Náchod, Hradec Králové Region, Tjekkiet, 54701
- Kailera Clinical Site
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Trutnov, Hradec Králové Region, Tjekkiet, 54101
- Kailera Clinical Site
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Prague
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Bohnice, Prague, Tjekkiet, 18100
- Kailera Clinical Site
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Prague, Prague, Tjekkiet, 14059
- Kailera Clinical Site
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South Moravian
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Brno, South Moravian, Tjekkiet, 60200
- Kailera Clinical Site
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Zlín
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Holešov, Zlín, Tjekkiet, 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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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
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 undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Ribupatide: Dose 1
Participants will receive Dose 1 of ribupatide once weekly. |
SC Injection
Andre navne:
|
|
Eksperimentel: Ribupatide: Dose 2
Participants will receive Dose 2 of ribupatide once weekly. |
SC Injection
Andre navne:
|
|
Eksperimentel: Ribupatide: Dose 3
Participants will receive Dose 3 of ribupatide once weekly. |
SC Injection
Andre navne:
|
|
Eksperimentel: Ribupatide: Dose 4
Participants will receive Dose 4 of ribupatide once weekly. |
SC Injection
Andre navne:
|
|
Placebo komparator: Placebo
Participants will receive placebo matched to ribupatide once weekly. |
SC Injection |
Hvad måler undersøgelsen?
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 |
|---|---|
|
Ændring fra baseline i taljeomkreds
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i absolut kropsvægt
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i systolisk blodtryk (SBP)
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentvis ændring fra udgangspunkt i fastende triglycerider
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentvis ændring fra baseline i fastende højdensitetslipoprotein (HDL)-kolesterol
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentvis ændring fra baseline i fastende ikke-HDL-kolesterol
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i påvirkningen af vægt på livskvalitet - lite kliniske forsøgsversion (IWQOL-Lite-CT) fysisk funktionssammensat score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentdel af deltagere med ≥30 % reduktion i kropsvægt
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i Control of Eating Questionnaire (CoEQ) Craving Control Score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ Positivt Humør-score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ-sult efter søde sager-score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ craving for saltet mad score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ Sult-score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ-mæthedsscore
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i CoEQ-kombineret score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i Food Noise Questionnaire (FNQ) score
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Antal deltagere med behandlingsrelaterede bivirkninger (TEAE'er)
Tidsramme: Dag 1 op til uge 80
|
Dag 1 op til uge 80
|
|
Antal deltagere med anti-lægemiddel-antistoffer (ADA'er)
Tidsramme: Op til uge 80
|
Op til uge 80
|
|
Antal deltagere med neutraliserende antistoffer (Nabs)
Tidsramme: Op til uge 80
|
Op til uge 80
|
|
Procentdel af deltagere med ≥5%, ≥10%, ≥15%, ≥20% og ≥25% reduktion i kropsvægt
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Ændring fra baseline i fastende blodsukker
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
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Deltagere med Body Mass Index (BMI) ≥35 Kilogram per Kvadratmeter (kg/m²): Procentvis Ændring fra Baseline i Kropsvægt
Tidsramme: Baseline, uge 76
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Baseline, uge 76
|
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Ændring fra baseline i BMI
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentdel af deltagere med HbA1c <5,7%
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
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Ændring fra baseline i diastolisk blodtryk (DBP)
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
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Procentvis ændring fra baseline i fastende totalt kolesterol
Tidsramme: Udgangsniveau, uge 76
|
Udgangsniveau, uge 76
|
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Procentvis ændring fra baseline i fastende lavtæthedslipoprotein (LDL)-kolesterol
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentvis ændring fra baseline i meget lavtæthedslipoprotein (VLDL)-kolesterol
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
|
Procentvis ændring fra baseline i fastende insulin
Tidsramme: Baseline, uge 76
|
Baseline, uge 76
|
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Doses 1 and 2 of Ribupatide Versus Placebo: Percent Change From Baseline in Body Weight at Week 76
Tidsramme: Baseline, Week 76
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Baseline, Week 76
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Doses 1 and 2 of Ribupatide Versus Placebo: Change From Baseline in HbA1c at Week 76
Tidsramme: Baseline, Week 76
|
Baseline, Week 76
|
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Percentage of Participants with HbA1c <7% and ≤6.5%
Tidsramme: Baseline, Week 76
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Baseline, Week 76
|
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Plasma Concentrations of Ribupatide
Tidsramme: Up to Week 76
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Up to Week 76
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studieleder: Medical Director, Kailera Therapeutics, Inc.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- K9531-3104
- 2025-523510-87-00 (Ctis)
- 2025 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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