A Study to Evaluate Effect of AZD6234 in Adult Participants With Type 2 Diabetes Mellitus and Obesity or Overweight (SELENE 2)
A Phase III Randomized, Double-Blind, Placebo-Controlled Multicentre Trial to Evaluate the Efficacy and Safety of AZD6234 in Participants With Type 2 Diabetes Mellitus and Obesity or Overweight (SELENE 2)
The study will evaluate how well AZD6234 works and how safe it is in adults with excess weight or obesity. Efficacy of AZD6234 will be compared to placebo in percent body weight change from baseline at 68 weeks of treatment
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
This is a Phase III, global, randomized, parallel-group, double-blind, multicentre study to assess the efficacy and safety of AZD6234 compared with placebo in adults with Type 2 Diabetes Mellitus (T2DM) and obesity or overweight. Eligible participants will be randomized to either receive AZD6234 or matching placebo respectively.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 3
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: AstraZeneca Clinical Study Information Center
- Telefonnummer: 1-877-240-9479
- E-mail: information.center@astrazeneca.com
Studiesteder
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Buenos Aires, Argentina, C1120AAC
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CABA, Argentina, C1425HFA
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Ciudad de Buenos Aires, Argentina, C1094AAD
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Mendoza, Argentina, 5500
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Ramos Mejía, Argentina, B1704ETD
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Rosario, Argentina, S2000PBJ
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San Nicolás, Argentina, B2900DMH
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Botany, Australien, 2019
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Camberwell, Australien, 3124
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Charlestown, Australien, 2290
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Helensvale, Australien, 4212
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Maroubra, Australien, 2035
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Waitara, Australien, 2077
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Alberta
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Calgary, Alberta, Canada, T3R 1W9
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British Columbia
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Vancouver, British Columbia, Canada, V5Y 3W2
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New Brunswick
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Moncton, New Brunswick, Canada, E1G 1A7
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Nova Scotia
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Truro, Nova Scotia, Canada, B2N 1L2
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Ontario
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Hamilton, Ontario, Canada, L8L 5G8
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Markham, Ontario, Canada, L3S 0A2
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North York, Ontario, Canada, M6B 3H7
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Sarnia, Ontario, Canada, N7T 4X3
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Scarborough Village, Ontario, Canada, M1R 0B1
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Stoney Creek, Ontario, Canada, L8J 3W2
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Stouffville, Ontario, Canada, L4A1H2
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Toronto, Ontario, Canada, M6G 1M2
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Toronto, Ontario, Canada, M4G3E8
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Quebec
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Joliette, Quebec, Canada, J6E 6A9
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Montreal, Quebec, Canada, H4N 2W2
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Montreal, Quebec, Canada, H4J 1E3
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Québec, Quebec, Canada, G2J 0C4
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Trois-Rivières, Quebec, Canada, G9A 4P3
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Concepción, Chile, 4070196
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Concepción, Chile, 4070060
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Concepción, Chile, 4070566
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Iquique, Chile, 1111442
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Las Condes, Chile, 6770128
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Providencia, Chile, 7500504
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Santiago, Chile, 7691236
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Santiago, Chile, 8331143
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Santiago, Chile, 7510187
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Chippenham, Det Forenede Kongerige, SN15 2SB
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Corby, Det Forenede Kongerige, NN17 2UR
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Corby, Det Forenede Kongerige, NN18 9EZ
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Dunfermline, Det Forenede Kongerige, KY12 0SU
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Hull, Det Forenede Kongerige, HU3 2PA
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Northwood, Det Forenede Kongerige, HA6 2RN
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Alabama
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Fairhope, Alabama, Forenede Stater, 36532
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Huntsville, Alabama, Forenede Stater, 35801
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Mobile, Alabama, Forenede Stater, 36608
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Mesa, Arizona, Forenede Stater, 85213
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Phoenix, Arizona, Forenede Stater, 85044
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Tucson, Arizona, Forenede Stater, 85715
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Arkansas
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Little Rock, Arkansas, Forenede Stater, 72205
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California
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Bakersfield, California, Forenede Stater, 93309
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Gardena, California, Forenede Stater, 90247
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Lincoln, California, Forenede Stater, 95648
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Torrance, California, Forenede Stater, 90503
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Walnut Creek, California, Forenede Stater, 94598
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Doral, Florida, Forenede Stater, 33172
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Fleming Island, Florida, Forenede Stater, 32003
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Fort Lauderdale, Florida, Forenede Stater, 33316
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Ocoee, Florida, Forenede Stater, 34761
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Woodstock, Georgia, Forenede Stater, 30189
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Illinois
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Chicago, Illinois, Forenede Stater, 60640
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Melrose Park, Illinois, Forenede Stater, 60160
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Oak Brook, Illinois, Forenede Stater, 60523
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Ames, Iowa, Forenede Stater, 50010
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Lenexa, Kansas, Forenede Stater, 66219
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Newton, Kansas, Forenede Stater, 67114
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Louisiana
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Monroe, Louisiana, Forenede Stater, 71201
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Beltsville, Maryland, Forenede Stater, 20705
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Lanham, Maryland, Forenede Stater, 20706
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Oxon Hill, Maryland, Forenede Stater, 20745
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Rockville, Maryland, Forenede Stater, 20852
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Massachusetts
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North Dartmouth, Massachusetts, Forenede Stater, 02747
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Michigan
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Farmington Hills, Michigan, Forenede Stater, 48336
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Mississippi
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Fayette, Mississippi, Forenede Stater, 39069
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Missouri
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Kansas City, Missouri, Forenede Stater, 64114
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Kansas City, Missouri, Forenede Stater, 64112
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St Louis, Missouri, Forenede Stater, 63141
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Nebraska
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Omaha, Nebraska, Forenede Stater, 68114
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Omaha, Nebraska, Forenede Stater, 68144
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New Jersey
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Eatontown, New Jersey, Forenede Stater, 07724
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Somerset, New Jersey, Forenede Stater, 08873
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Warren Township, New Jersey, Forenede Stater, 07059
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North Carolina
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Greensboro, North Carolina, Forenede Stater, 27408
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Monroe, North Carolina, Forenede Stater, 28112
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Ohio
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Stow, Ohio, Forenede Stater, 44224
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Scottdale, Pennsylvania, Forenede Stater, 15683
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Tennessee
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Franklin, Tennessee, Forenede Stater, 37067
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Jackson, Tennessee, Forenede Stater, 38305
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Knoxville, Tennessee, Forenede Stater, 37938
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Texas
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DeSoto, Texas, Forenede Stater, 75115
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El Paso, Texas, Forenede Stater, 79935
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Houston, Texas, Forenede Stater, 77099
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Midland, Texas, Forenede Stater, 79707
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Pasadena, Texas, Forenede Stater, 77504
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San Antonio, Texas, Forenede Stater, 78215
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San Antonio, Texas, Forenede Stater, 78258
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San Antonio, Texas, Forenede Stater, 78207
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Virginia
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Manassas, Virginia, Forenede Stater, 20110
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Norfolk, Virginia, Forenede Stater, 23504
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Bangalore, Indien, 560092
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Indore, Indien, 452010
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Kolkata, Indien, 700014
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Nagpur, Indien, 440010
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Noida, Indien, 201310
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Pune, Indien, 411021
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Pune, Indien, 411057
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Siliguri, Indien, 734012
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Visakhapatnam, Indien, 530002
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Aira, Japan, 899-5421
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Chūōku, Japan, 1040031
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Fukuoka, Japan, 814-0153
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Hachioji-shi, Japan, 192-0071
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Izunokuni-shi, Japan, 410-2295
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Kumamoto, Japan, 860-0833
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Nagoya, Japan, 451-8511
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Nagoya, Japan, 467-0806
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Nerima-ku, Japan, 177-0051
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Osaka, Japan, 540-0006
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Osaka, Japan, 537-0014
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Saga, Japan, 840-8571
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Sapporo, Japan, 060-0001
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Shinjuku-ku, Japan, 160-0008
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Suita-shi, Japan, 565-0853
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Tanabe-shi, Japan, 646-8558
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Beijing, Kina, 100050
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Cangzhou, Kina, 061001
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Changchun, Kina, 130011
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Chengdu, Kina, 610072
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Chengdu, Kina, 610021
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Danyang, Kina, 212399
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Ganzhou, Kina, 341000
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Guangzhou, Kina, 510280
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Huizhou, Kina, 516002
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Huzhou, Kina, 313003
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Lanzhou, Kina, 730000
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Nanjing, Kina, 210008
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Nanjing, Kina, 210009
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Panjin, Kina, 124009
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Suzhou, Kina, 215006
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Xianyang, Kina, 712000
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Bialystok, Polen, 15-481
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Elblag, Polen, 82-300
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Gdynia, Polen, 81-338
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Katowice, Polen, 40-081
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Katowice, Polen, 40-772
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Krakow, Polen, 30-105
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Krakow, Polen, 31-271
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Legnica, Polen, 59-220
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Lodz, Polen, 90-338
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Lodz, Polen, 90-132
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Poznan, Polen, 60-354
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Radzionków, Polen, 41-922
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Warsaw, Polen, 00-719
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Warsaw, Polen, 03-291
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Wroclaw, Polen, 53-673
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Bratislava, Slovakiet, 831 03
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Bratislava, Slovakiet, 83106
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Košice, Slovakiet, 040 01
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Košice, Slovakiet, 04022
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Lučenec, Slovakiet, 984 01
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Námestovo, Slovakiet, 02901
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Prievidza, Slovakiet, 97101
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Rožňava, Slovakiet, 048 01
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Trebišov, Slovakiet, 075 01
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A Coruña, Spanien, 15006
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Alzira (Valencia), Spanien, 46600
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Barcelona, Spanien, 08035
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Castilleja de La Cuesta, Sevilla, Spanien, 41950
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Ferrol (A Coruña), Spanien, 15404
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Lleida, Spanien, 25198
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Málaga, Spanien, 29010
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Oviedo, Spanien, 33011
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Segovia, Spanien, 40002
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Seville, Spanien, 41010
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Busan, Sydkorea, 48108
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Daegu, Sydkorea, 42601
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Daejeon, Sydkorea, 35233
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Incheon, Sydkorea, 403-720
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Seoul, Sydkorea, 06351
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Seoul, Sydkorea, 01830
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Seoul, Sydkorea, 08308
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Seoul, Sydkorea, 150-713
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Seoul, Sydkorea, 143729
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Suwon, Sydkorea, 16247
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Changhua, Taiwan, 500
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Kaohsiung City, Taiwan, 80756
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Taichung, Taiwan, 404
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Taichung, Taiwan, 402
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Taichung, Taiwan, 433004
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Taichung, Taiwan, 407219
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Tainan, Taiwan, 710
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Tainan, Taiwan, 704
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Taipei, Taiwan, 10002
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Taipei, Taiwan, 11490
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Zhubei, Taiwan, 302
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Berlin, Tyskland, 10117
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Berlin, Tyskland, 10629
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Bochum, Tyskland, 44789
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Bünde, Tyskland, 32257
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Dresden, Tyskland, 01069
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Frankfurt, Tyskland, 60596
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Frankfurt, Tyskland, 60590
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Freiburg im Breisgau, Tyskland, 79106
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Göttingen, Tyskland, 37075
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Hamburg, Tyskland, 20095
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Hamburg, Tyskland, 20253
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Hanover, Tyskland, 30159
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Homburg, Tyskland, 66421
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Jerichow, Tyskland, 39319
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Karlsruhe, Tyskland, 76137
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Leipzig, Tyskland, 04177
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Magdeburg, Tyskland, 39110
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Mainz, Tyskland, 55128
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München, Tyskland, 80339
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Offenbach, Tyskland, 63065
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Balatonfüred, Ungarn, 8230
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Budapest, Ungarn, 1036
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Budapest, Ungarn, 1024
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Budapest, Ungarn, 1132
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Budapest, Ungarn, 1138
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Debrecen, Ungarn, 4031
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Debrecen, Ungarn, 4032
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Miskolc, Ungarn, 3530
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Nyíregyháza-Sóstóhegy, Ungarn, 4481
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Szeged, Ungarn, 6725
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- Research Site
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Szolnok, Ungarn, 5000
- Trukket tilbage
- Research Site
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Males & females (inclusive of all gender identities) age ≥18 years
- BMI ≥27 kg/m2
- Diagnosed with T2DM ≥90 days prior to Screening
- HbA1c value at Screening of ≥6.0% (42 mmol/mol) and ≤10% (86 mmol/mol) managed with diet and exercise alone or with a stable dose of any oral glycaemic-lowering agent (as per local labelling)
- Stable body weight (≤5% body weight change) for at least 3 months prior to Randomisation
- History of at least one self-reported unsuccessful attempt to lose body weight in lifetime
Exclusion Criteria:
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Obesity primarily caused by other endocrine disorders
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Type 1 diabetes mellitus (or any other diabetes mellitus that is not clearly Type 2 diabetes), OR have history of ketoacidosis or hyperosmolar coma/state within 3 months prior to Screening
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Significant hepatobiliary disease and/or any of the following results at Screening:
- ALT ≥ 3.0 X ULN
- AST ≥ 3.0 X ULN
- TBL > 1.5 X ULN (except for cases of known Gilbert's Syndrome)
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Has received treatment with a GLP-1 receptor agonist or GLP-1 containing medication for any indication within 3 months before Randomisation
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Use of insulin therapy for T2DM within 3 months prior to screening
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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Placebo komparator: Placebo
Matching placebo |
Placebo matching IMP dose injected subcutaneously, once a week. |
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Eksperimentel: AZD6234 Dose 1
AZD6234 Dose 1 |
IMP injected subcutaneously, once a week. Unit dose strength as per CSP.
Andre navne:
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Eksperimentel: AZD6234 Dose 2
AZD6234 Dose 2 |
IMP injected subcutaneously, once a week. Unit dose strength as per CSP.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Percent change in body weight from baseline at 68 weeks of treatment.
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo in percent body weight change |
68 weeks
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Absolute change in weight (kg) from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo on absolute change in weight |
68 weeks
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Achievement of at least 5 % body weight loss from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo in body weight loss of at least 5% |
68 weeks
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Achievement of at least 10 % body weight loss from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo in body weight loss of at least 10% |
68 weeks
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Change in haemoglobin A1C from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 on haemoglobin A1C change |
68 weeks
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Change in waist circumference (cm) from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo on waist circumference change |
68 weeks
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Percent change in triglycerides from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo on triglycerides percent change |
68 weeks
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Change in systolic blood pressure (mmHg) from baseline at 68 weeks of treatment
Tidsramme: 68 weeks
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To evaluate the effect of AZD6234 compared to placebo on systolic blood pressure change |
68 weeks
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Percent change in fat mass from baseline at 68 weeks of treatment measured by DXA in the DXA Sub-Study subset
Tidsramme: 68 weeks
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Body Composition Sub-study: To evaluate the effect of AZD6234 compared to placebo on body composition change in the DXA subset of participants |
68 weeks
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- D8750C00012
- 159494 (Registry Identifier: IND Number)
- 2025 (U.S. NIH-bevilling/kontrakt)
- 2025-524616-11 (Registry Identifier: CTIS (EU))
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.
IPD-delingstidsramme
AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA PhRMA Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD-delingsadgangskriterier
When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org. Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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