一项评估化疗联合或不联合INCB161734治疗既往未经治疗的KRAS G12D突变转移性胰腺导管腺癌的研究 (DAWN-303)
一项针对既往未治疗的KRAS G12D突变转移性胰腺导管腺癌患者化疗联合或不联合INCB161734的随机、双盲、3期研究(DAWN-303)
The purpose of this study is to evaluate the efficacy and safety of standard chemotherapy with or without INCB161734 in participants with metastatic pancreatic ductal adenocarcinoma (PDAC).
研究概览
地位
地位
干预/治疗
干预/治疗
研究类型
研究类型
注册 (估计的)
注册
阶段
阶段
- 第三阶段
联系人和位置
学习联系方式
学习联系方式
- 姓名:Incyte Corporation Call Center (US)
- 电话号码:1.855.463.3463
- 邮箱:medinfo@incyte.com
研究联系人备份
- 姓名:Incyte Corporation Call Center (ex-US)
- 电话号码:+800 00027423
- 邮箱:eumedinfo@incyte.com
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Bonn、德国、53127
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Cologne、德国、D-50937
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Dresden、德国、01307
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Düsseldorf、德国、40225
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Essen、德国、45147
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Frankfurt、德国、60488
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Freiburg im Breisgau、德国、79106
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Göttingen、德国、37075
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Halle、德国、06120
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Hamburg、德国、20251
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Leipzig、德国、04103
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Munich、德国、81377
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München、德国、81737
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Nuremberg、德国、90419
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Ulm、德国、89081
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Bologna、意大利、40138
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Brescia、意大利、25124
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Candiolo、意大利、10060
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Foggia、意大利、71122
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Milan、意大利、20133
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Milan、意大利、20132
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Naples、意大利、80131
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Pisa、意大利、56126
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Roma、意大利、00152
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Rome、意大利、00138
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Rozzano、意大利、20089
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Verona、意大利、37134
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Bergen、挪威、05021
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Oslo、挪威、00379
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Stavanger、挪威、04011
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Trondheim、挪威、07030
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Auckland、新西兰、01023
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Akashi, HYGO、日本、673-0021
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Fukuoka Fukuoka、日本、812-0054
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Kahoku-gun、日本、920-0293
- 招聘中
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Kitaadachi-gun、日本、362-0806
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- Investigative Site JP014
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Kōtoku、日本、135-8550
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Mitaka-shi、日本、181-8611
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Osaka、日本、541-8567
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Sapporo Hokkaido、日本、060-0814
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Shinjuku-ku、日本、160-0023
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Suita, Osaka、日本、565-0871
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Toyama、日本、930-0194
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Wakayama、日本、641-8510
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Yokohama、日本、241-8515
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Anderlecht、比利时、01070
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Brussels、比利时、01090
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Brussels、比利时、01200
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Edegem、比利时、02650
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Ghent、比利时、09000
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Gilly、比利时、06060
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Leuven、比利时、03000
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Liège、比利时、04000
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Yvoir、比利时、05530
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Brest、法国、29200
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Dijon、法国、21000
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Lille、法国、59037
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Lyon、法国、69008
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Lyon、法国、69373
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Marseille、法国、13385
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Montpellier、法国、34298
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Paris、法国、75013
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Paris、法国、75015
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Pessac、法国、33604
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Poitiers、法国、86021
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Reims、法国、51100
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Rennes、法国、35042
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Toulouse、法国、31059
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Tours、法国、37000
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Villejuif、法国、94805
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Gdansk、波兰、80-214
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Krakow、波兰、31-501
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Warsaw、波兰、02-507
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Warsaw、波兰、01-748
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Warsaw、波兰、02-034
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Wroclaw、波兰、53-439
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Dorado、波多黎各、00646
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Canberra、澳大利亚、02605
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Perth、澳大利亚、06009
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Macquarie Park、New South Wales、澳大利亚、02109
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Queensland
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Chermside、Queensland、澳大利亚、04032
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Townsville、Queensland、澳大利亚、04814
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South Australia
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Woodville South、South Australia、澳大利亚、05011
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Melbourne、Victoria、澳大利亚、03000
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Richmond、Victoria、澳大利亚、03121
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Linköping、瑞典、58185
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Stockholm、瑞典、17176
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Basel、瑞士、04058
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Bern、瑞士、03010
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Geneva、瑞士、01205
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Lausanne、瑞士、01011
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Zurich、瑞士、08091
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Birmingham、Alabama、美国、35233
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Arizona
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Chandler、Arizona、美国、85224
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Tucson、Arizona、美国、85719
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California
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Duarte、California、美国、91010
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Fullerton、California、美国、92835
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La Jolla、California、美国、92093
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Long Beach、California、美国、90806-1650
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Los Angeles、California、美国、90089
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Orange、California、美国、92868
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San Francisco、California、美国、94143
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Santa Monica、California、美国、90404
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Colorado
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Denver、Colorado、美国、80218
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District of Columbia
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Washington D.C.、District of Columbia、美国、20007
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Washington D.C.、District of Columbia、美国、20016
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Florida
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Fort Myers、Florida、美国、33901
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Jacksonville、Florida、美国、32207
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Miami、Florida、美国、33136
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St. Petersburg、Florida、美国、33701-4553
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West Palm Beach、Florida、美国、33401
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Georgia
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Atlanta、Georgia、美国、30322
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Illinois
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Chicago、Illinois、美国、60637
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Evanston、Illinois、美国、60201
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Naperville、Illinois、美国、60540
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Springfield、Illinois、美国、62702
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Indiana
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Indianapolis、Indiana、美国、46250
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Louisiana
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New Orleans、Louisiana、美国、70121
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Massachusetts
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Boston、Massachusetts、美国、02215
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Michigan
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Ann Arbor、Michigan、美国、48109-9001
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Detroit、Michigan、美国、48201
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Grand Rapids、Michigan、美国、49503
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Ypsilanti、Michigan、美国、48197
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Minnesota
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Maple Grove、Minnesota、美国、55369
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Mississippi
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Hattiesburg、Mississippi、美国、39401
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Nevada
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Reno、Nevada、美国、89502
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New Jersey
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Hackensack、New Jersey、美国、07601
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Morristown、New Jersey、美国、07960
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New York
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Lake Success、New York、美国、11042
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New York、New York、美国、10065
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- Investigative Site US003
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New York、New York、美国、10016
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- Investigative Site US031
-
New York、New York、美国、10128
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- Investigative Site US041
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The Bronx、New York、美国、10461
- 招聘中
- Investigative Site US029
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North Carolina
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Chapel Hill、North Carolina、美国、27514
- 招聘中
- Investigative Site US035
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Ohio
-
Cleveland、Ohio、美国、44195
- 招聘中
- Investigative Site US020
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Cleveland、Ohio、美国、44106
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- Investigative Site US050
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Columbus、Ohio、美国、43210
- 尚未招聘
- Investigative Site US033
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Oregon
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Portland、Oregon、美国、97239
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- Investigative Site US042
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Pennsylvania
-
Philadelphia、Pennsylvania、美国、19104
- 招聘中
- Investigative Site US008
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Philadelphia、Pennsylvania、美国、19107
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- Investigative Site US043
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Pittsburgh、Pennsylvania、美国、15212
- 招聘中
- Investigative Site US056
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South Carolina
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Charleston、South Carolina、美国、29425
- 尚未招聘
- Investigative Site US082
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South Dakota
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Sioux Falls、South Dakota、美国、57105-2140
- 招聘中
- Investigative Site US055
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Tennessee
-
Nashville、Tennessee、美国、37203
- 招聘中
- Investigative Site US060
-
Nashville、Tennessee、美国、37203
- 招聘中
- Investigative Site US039
-
Nashville、Tennessee、美国、37232-6309
- 招聘中
- Investigative Site US070
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Texas
-
Dallas、Texas、美国、75246
- 招聘中
- Investigative Site US067
-
Denison、Texas、美国、75020
- 招聘中
- Investigative Site US062
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Houston、Texas、美国、77030
- 招聘中
- Investigative Site US011
-
San Antonio、Texas、美国、78240
- 招聘中
- Investigative Site US063
-
San Antonio、Texas、美国、78229
- 尚未招聘
- Investigative Site US080
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Utah
-
Salt Lake City、Utah、美国、84112
- 招聘中
- Investigative Site US053
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Virginia
-
Fairfax、Virginia、美国、22031
- 尚未招聘
- Investigative Site US057
-
Fairfax、Virginia、美国、22031
- 招聘中
- Investigative Site US065
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Salem、Virginia、美国、24153
- 招聘中
- Investigative Site US064
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Washington
-
Olympia、Washington、美国、98506
- 招聘中
- Investigative Site US081
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Seattle、Washington、美国、98104
- 招聘中
- Investigative Site US032
-
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Wisconsin
-
Madison、Wisconsin、美国、53792
- 招聘中
- Investigative Site US044
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-
-
-
-
HUS、芬兰、00290
- 招聘中
- Investigative Site FI001
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Tampere、芬兰、33521
- 招聘中
- Investigative Site FI003
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Turku、芬兰、20521
- 尚未招聘
- Investigative Site FI002
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-
-
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Dundee、英国、DD1 9SY
- 招聘中
- Investigative Site GR008
-
Guildford、英国、GU2 7XX
- 尚未招聘
- Investigative Site GB011
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Headington、英国、OX3 7LE
- 尚未招聘
- Investigative Site GB002
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Leeds、英国、LS9 7TF
- 尚未招聘
- Investigative Site GB001
-
London、英国、NW3 2QG
- 尚未招聘
- Investigative Site GB004
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London、英国、EC1A 7BE
- 招聘中
- Investigative Site GB009
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Manchester、英国、M20 4BX
- 尚未招聘
- Investigative Site GB003
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Northwood、英国、HA6 2RN
- 尚未招聘
- Investigative Site GB010
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Norwich、英国、NR4 7UY
- 尚未招聘
- Investigative Site GB005
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-
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Amsterdam、荷兰、1081 HV
- 招聘中
- Investigative Site NL001
-
Eindhoven、荷兰、5623 EJ
- 招聘中
- Investigative Site NL007
-
Groningen、荷兰、9700 RB
- 招聘中
- Investigative Site NL005
-
Maastricht、荷兰、6229 HX
- 招聘中
- Investigative Site NL003
-
Utrecht、荷兰、3543 AZ
- 招聘中
- Investigative Site NL006
-
-
-
-
-
Badalona、西班牙、08916
- 尚未招聘
- Investigative Site ES011
-
Barcelona、西班牙、08035
- 尚未招聘
- Investigative Site ES003
-
Barcelona、西班牙、08011
- 招聘中
- Investigative Site ES002
-
Las Palmas de Gran Canaria、西班牙、35016
- 招聘中
- Investigative Site ES014
-
Madrid、西班牙、28041
- 招聘中
- Investigative Site ES008
-
Madrid、西班牙、28034
- 尚未招聘
- Investigative Site ES006
-
Madrid、西班牙、28040
- 尚未招聘
- Investigative Site ES012
-
Madrid、西班牙、28009
- 招聘中
- Investigative Site ES016
-
Madrid、西班牙、28040
- 招聘中
- Investigative Site ES007
-
Madrid、西班牙、28050
- 招聘中
- Investigative Site ES013
-
Palma de Mallorca、西班牙、07120
- 尚未招聘
- Investigative Site ES005
-
Santander、西班牙、39008
- 招聘中
- Investigative Site ES009
-
Seville、西班牙、41009
- 尚未招聘
- Investigative Site ES010
-
Valencia、西班牙、46009
- 尚未招聘
- Investigative Site ES015
-
Valencia、西班牙、46010
- 尚未招聘
- Investigative Site ES017
-
Valencia、西班牙、46014
- 招聘中
- Investigative Site ES001
-
Zaragoza、西班牙、50009
- 招聘中
- Investigative Site ES004
-
-
-
-
-
Goyang-si、韩国、10408
- 招聘中
- Investigative Site KR004
-
Seongnam-si、韩国、13496
- 招聘中
- Investigative Site KR007
-
Seongnam-si、韩国、13620
- 招聘中
- Investigative Site KR005
-
Seoul、韩国、06591
- 尚未招聘
- Investigative Site KR008
-
Seoul、韩国、03080
- 招聘中
- Investigative Site KR002
-
Seoul、韩国、05505
- 招聘中
- Investigative Site KR001
-
Seoul、韩国、03722
- 招聘中
- Investigative Site KR006
-
Seoul、韩国、06351
- 招聘中
- Investigative Site KR003
-
-
参与标准
资格标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Histologically or cytologically confirmed metastatic PDAC with a KRAS G12D mutation
- No prior systemic treatment in the metastatic setting
- ECOG Performance status 0-1
- Adequate organ function
Exclusion Criteria:
- Prior treatment with any KRAS inhibitor
- Chronic or current active infection requiring systemic treatment within 1 week prior to the first dose of study drug
- Known active CNS metastases
Other protocol-defined Inclusion/Exclusion Criteria may apply.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
手臂数量
武器和干预
参与者组/臂参与者组/臂 |
干预/治疗干预/治疗 |
|---|---|
|
实验性的:INCB161734 plus chemotherapy
INCB161734 at the protocol-defined dose with investigator's choice of chemotherapy (mFOLFIRINOX or GemNabP) in accordance with the protocol-defined requirements. |
Oral; tablet The investigator will select the chemotherapy in accordance with the protocol-defined requirements. The possible choices as defined by the protocol:
其他名称:
|
|
实验性的:Placebo plus chemotherapy
Placebo at the protocol-defined dose with investigator's choice of chemotherapy (mFOLFIRINOX or GemNabP) in accordance with the protocol-defined requirements. |
The investigator will select the chemotherapy in accordance with the protocol-defined requirements. The possible choices as defined by the protocol:
其他名称:
Oral; tablet |
研究衡量的是什么?
主要结果指标
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Overall Survival (OS)
大体时间:Up to approximately 3 years
|
Defined as the time from the date of randomization to the date of death due to any cause. |
Up to approximately 3 years
|
|
Progression-free survival (PFS) by BICR
大体时间:Up to approximately 2 years
|
Defined as the time from the date of randomization to the date of the first documented progression as determined by blinded independent central review (BICR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 or death due to any cause. |
Up to approximately 2 years
|
|
Objective Response by BICR
大体时间:Up to approximately 2 years
|
Defined as complete response (CR) or partial response (PR) as determined by BICR per RECIST v1.1. |
Up to approximately 2 years
|
次要结果测量
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Duration of Response (DOR) by BICR
大体时间:Up to approximately 2 years
|
Defined as the time from the earliest date of documented response until the earliest date of disease progression as determined by BICR per RECIST v1.1 or death from any cause. |
Up to approximately 2 years
|
|
Disease control by BICR
大体时间:Up to approximately 2 years
|
Defined as having CR, PR, or stable disease (SD) as the best response determined by BICR per RECIST v1.1. |
Up to approximately 2 years
|
|
Progression-Free Survival (PFS) by investigator assessment
大体时间:Up to approximately 2 years
|
Defined as the time from the date of randomization to the date of the first documented progression as determined by the investigator per RECIST v1.1 or death due to any cause. |
Up to approximately 2 years
|
|
Objective response by investigator assessment
大体时间:Up to approximately 2 years
|
Defined as CR or PR as determined by the investigator per RECIST v1.1. |
Up to approximately 2 years
|
|
DOR by investigator assessment
大体时间:Up to approximately 2 years
|
Defined as the time from the earliest date of documented response until earliest date of disease progression as determined by the investigator per RECIST v1.1 or death from any cause. |
Up to approximately 2 years
|
|
Disease control by investigator assessment
大体时间:Up to approximately 2 years
|
Defined as having CR, PR, or SD as the best response as determined by the investigator per RECIST v1.1. |
Up to approximately 2 years
|
|
Treatment Emergent Adverse Events (TEAEs)
大体时间:Up to approximately 2 years and 30 days
|
Adverse events reported for the first time or worsening of a pre-existing event after first dose of study drug until 30 days after the last dose of study drug or the start of new anticancer therapy, whichever occurs first. |
Up to approximately 2 years and 30 days
|
|
TEAEs leading to dose interruptions, dose reductions or discontinuation of study treatment
大体时间:Up to approximately 2 years and 30 days
|
TEAEs leading to dose interruptions, dose reductions or discontinuation of study treatment. |
Up to approximately 2 years and 30 days
|
|
Change from baseline in European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ)-Core 30 (C30) at each postbaseline visit
大体时间:Up to approximately 2 years
|
The EORTC QLQ-C30 is a validated, self-administered questionnaire developed to assess the quality of life in cancer patients. It consists of 30 questions divided into several subscales, including 5 functional scales (physical, role, cognitive, emotional, and social), 3 symptom scales (fatigue, nausea and vomiting, and pain), a global health status/QoL scale, and a number of single-item measures that assess additional symptoms such as dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties. |
Up to approximately 2 years
|
|
Change from baseline in EORTC QLQ-PAN26 score at each postbaseline visit
大体时间:Up to approximately 2 years
|
The EORTC QLQ-PAN26 consists of 26 questions that assess 9 pancreatic cancer-related and treatment-related symptoms (pain, eating-related items, cachexia, hepatic symptoms, side effects, altered bowel habits, ascites, indigestion, and flatulence) and 5 emotional domains specific to pancreatic cancer (body image, healthcare satisfaction, sexuality, fear of future health, and ability to plan for the future). The QLQ-PAN26 is scored on a 4-point scale that ranges from not at all to very much. |
Up to approximately 2 years
|
|
Change from baseline in EQ-5D-5L score at each postbaseline visit
大体时间:Up to approximately 2 years
|
The EQ-5D-5L is a validated, self-reported instrument for assessing HRQoL across 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 response levels of severity, ranging from no problems to extreme problems. The questionnaire also includes a visual analog scale for self-rated overall health on a scale from 0 (worst imaginable health) to 100 (best imaginable health). |
Up to approximately 2 years
|
合作者和调查者
调查人员
调查人员
- 研究主任:Incyte Medical Monitor、Incyte Corporation
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
学习开始
初级完成 (估计的)
初级完成
研究完成 (估计的)
研究完成
研究注册日期
首次提交
首次提交
首先提交符合 QC 标准的
首先提交符合 QC 标准的
首次发布 (实际的)
首次发布
研究记录更新
最后更新发布 (实际的)
最后更新发布
上次提交的符合 QC 标准的更新
上次提交的符合 QC 标准的更新
最后验证
最后验证
更多信息
与本研究相关的术语
其他研究编号
其他研究编号
- INCB161734-303
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Incyte shares data with qualified external researchers after a research proposal is submitted. These requests are reviewed and approved by a review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. The trial data availability is according to the criteria and process described on https://www.incyte.com/our-company/compliance-and-transparency
IPD 共享时间框架
Data will be shared after the primary publication or 2 years after the study has ended for market authorized products and indications.
IPD 共享访问标准
Data from eligible studies will be shared with qualified researchers according to the criteria and process described in the Data Sharing section of the www.incyteclinicaltrials.com website. For approved requests, the researchers will be granted access to anonymized data under the terms of a data sharing agreement.
IPD 共享支持信息类型
- 研究方案
- 树液
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.