- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT00267748
Sunitinib Malate Schedule 4/2 vs. Sunitinib Malate Continuous Dosing As First-Line Therapy For Metastatic Renal Cell Cancer (RCC)
A Randomized Phase II Study Of The Efficacy And Safety Of Sunitinib Malate Schedule 4/2 vs. Sunitinib Malate Continuous Dosing As First-Line Therapy For Metastatic Renal Cell Cancer (Renal EFFECT Trial)
This trial has two parts. The purpose of the first part of the trial is to determine the doses of 2 drugs, sunitinib malate and interferon alfa-2b, that can be given safely in combination. This part is currently closed to enrollment.
The purpose of the second part of the trial is to see if sunitinib malate given on a 4/2 schedule (4 weeks on treatment, 2 weeks off treatment cycle) is any better at delaying progression of renal cell cancer than sunitinib malate given on a continuous dosing schedule. The trial will also determine the number of patients whose cancer responds to the treatments, whether life of patients can be extended, what the side effects are of the treatments, how bothersome disease or treatment-related symptoms are to patients, and whether tests can be found that will predict which patients may or may not respond to these treatments in the future.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 2
Kontakty i lokalizacje
Lokalizacje studiów
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Arkansas
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Hot Springs, Arkansas, Stany Zjednoczone, 71913
- Pfizer Investigational Site
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Little Rock, Arkansas, Stany Zjednoczone, 72205
- Pfizer Investigational Site
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California
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Anaheim, California, Stany Zjednoczone, 92807
- Pfizer Investigational Site
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Baldwin Park, California, Stany Zjednoczone, 91706
- Pfizer Investigational Site
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Bellflower, California, Stany Zjednoczone, 90706
- Pfizer Investigational Site
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Duarte, California, Stany Zjednoczone, 91010
- Pfizer Investigational Site
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Fontana, California, Stany Zjednoczone, 92335
- Pfizer Investigational Site
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Irvine, California, Stany Zjednoczone, 92618
- Pfizer Investigational Site
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Los Angeles, California, Stany Zjednoczone, 90095
- Pfizer Investigational Site
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Los Angeles, California, Stany Zjednoczone, 90027
- Pfizer Investigational Site
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Los Angeles, California, Stany Zjednoczone, 90034
- Pfizer Investigational Site
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Panorama City, California, Stany Zjednoczone, 91402
- Pfizer Investigational Site
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Riverside, California, Stany Zjednoczone, 92505
- Pfizer Investigational Site
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San Diego, California, Stany Zjednoczone, 92108
- Pfizer Investigational Site
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San Diego, California, Stany Zjednoczone, 92120
- Pfizer Investigational Site
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Woodland Hills, California, Stany Zjednoczone, 91365
- Pfizer Investigational Site
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Colorado
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Aurora, Colorado, Stany Zjednoczone, 80012
- Pfizer Investigational Site
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Boulder, Colorado, Stany Zjednoczone, 80304
- Pfizer Investigational Site
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Boulder, Colorado, Stany Zjednoczone, 80303
- Pfizer Investigational Site
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Colorado Springs, Colorado, Stany Zjednoczone, 80909
- Pfizer Investigational Site
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Denver, Colorado, Stany Zjednoczone, 80220
- Pfizer Investigational Site
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Denver, Colorado, Stany Zjednoczone, 80218
- Pfizer Investigational Site
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Lakewood, Colorado, Stany Zjednoczone, 80228
- Pfizer Investigational Site
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Littleton, Colorado, Stany Zjednoczone, 80120
- Pfizer Investigational Site
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Lone Tree, Colorado, Stany Zjednoczone, 80124
- Pfizer Investigational Site
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Longmont, Colorado, Stany Zjednoczone, 80501
- Pfizer Investigational Site
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Parker, Colorado, Stany Zjednoczone, 80138
- Pfizer Investigational Site
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Pueblo, Colorado, Stany Zjednoczone, 81008
- Pfizer Investigational Site
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Thorton, Colorado, Stany Zjednoczone, 80260
- Pfizer Investigational Site
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Connecticut
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Norwich, Connecticut, Stany Zjednoczone, 06360
- Pfizer Investigational Site
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Delaware
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Newark, Delaware, Stany Zjednoczone, 19718
- Pfizer Investigational Site
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Newark, Delaware, Stany Zjednoczone, 19713
- Pfizer Investigational Site
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Wilmington, Delaware, Stany Zjednoczone, 19899
- Pfizer Investigational Site
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Florida
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Boca Raton, Florida, Stany Zjednoczone, 33486
- Pfizer Investigational Site
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Delray Beach, Florida, Stany Zjednoczone, 33484
- Pfizer Investigational Site
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Lakeland, Florida, Stany Zjednoczone, 33805
- Pfizer Investigational Site
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Orlando, Florida, Stany Zjednoczone, 32806
- Pfizer Investigational Site
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Georgia
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Columbus, Georgia, Stany Zjednoczone, 31902
- Pfizer Investigational Site
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Columbus, Georgia, Stany Zjednoczone, 31904
- Pfizer Investigational Site
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Idaho
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Boise, Idaho, Stany Zjednoczone, 83712
- Pfizer Investigational Site
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Indiana
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Elkhart, Indiana, Stany Zjednoczone, 46514
- Pfizer Investigational Site
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Jefferson, Indiana, Stany Zjednoczone, 47130
- Pfizer Investigational Site
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Kokomo, Indiana, Stany Zjednoczone, 46902-3803
- Pfizer Investigational Site
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La Porte, Indiana, Stany Zjednoczone, 46350
- Pfizer Investigational Site
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LaPorte, Indiana, Stany Zjednoczone, 46350
- Pfizer Investigational Site
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LaPorte, Indiana, Stany Zjednoczone, 46350-5533
- Pfizer Investigational Site
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Michigan City, Indiana, Stany Zjednoczone, 46360
- Pfizer Investigational Site
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Plymouth, Indiana, Stany Zjednoczone, 46563
- Pfizer Investigational Site
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South Bend, Indiana, Stany Zjednoczone, 46601
- Pfizer Investigational Site
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South Bend, Indiana, Stany Zjednoczone, 46617
- Pfizer Investigational Site
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Iowa
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Cedar Rapids, Iowa, Stany Zjednoczone, 52402
- Pfizer Investigational Site
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Kentucky
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Lexington, Kentucky, Stany Zjednoczone, 40536
- Pfizer Investigational Site
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Lexington, Kentucky, Stany Zjednoczone, 40536-0293
- Pfizer Investigational Site
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Louisville, Kentucky, Stany Zjednoczone, 40202
- Pfizer Investigational Site
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Louisville, Kentucky, Stany Zjednoczone, 40217
- Pfizer Investigational Site
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Louisville, Kentucky, Stany Zjednoczone, 40207
- Pfizer Investigational Site
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Shelbyville, Kentucky, Stany Zjednoczone, 40065
- Pfizer Investigational Site
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Louisiana
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Baton Rouge, Louisiana, Stany Zjednoczone, 70809
- Pfizer Investigational Site
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Covington, Louisiana, Stany Zjednoczone, 70433
- Pfizer Investigational Site
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Gretna, Louisiana, Stany Zjednoczone, 70056
- Pfizer Investigational Site
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Marrero, Louisiana, Stany Zjednoczone, 70072
- Pfizer Investigational Site
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Metairie, Louisiana, Stany Zjednoczone, 70006
- Pfizer Investigational Site
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New Orleans, Louisiana, Stany Zjednoczone, 70115
- Pfizer Investigational Site
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Shreveport, Louisiana, Stany Zjednoczone, 71103
- Pfizer Investigational Site
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Maryland
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Baltimore, Maryland, Stany Zjednoczone, 21201
- Pfizer Investigational Site
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Baltimore, Maryland, Stany Zjednoczone, 21237
- Pfizer Investigational Site
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Bethesda, Maryland, Stany Zjednoczone, 20817
- Pfizer Investigational Site
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Michigan
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Grand Rapids, Michigan, Stany Zjednoczone, 49503
- Pfizer Investigational Site
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Holland, Michigan, Stany Zjednoczone, 49424
- Pfizer Investigational Site
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Niles, Michigan, Stany Zjednoczone, 49120
- Pfizer Investigational Site
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Saint Joseph, Michigan, Stany Zjednoczone, 49085
- Pfizer Investigational Site
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St. Joseph, Michigan, Stany Zjednoczone, 49085
- Pfizer Investigational Site
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St. Joseph, Michigan, Stany Zjednoczone, 49085-2112
- Pfizer Investigational Site
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St. Joseph, Michigan, Stany Zjednoczone, 49085-2158
- Pfizer Investigational Site
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Missouri
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Saint Louis, Missouri, Stany Zjednoczone, 63141
- Pfizer Investigational Site
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St. Louis, Missouri, Stany Zjednoczone, 63141
- Pfizer Investigational Site
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Washington, Missouri, Stany Zjednoczone, 63090
- Pfizer Investigational Site
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Nevada
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Henderson, Nevada, Stany Zjednoczone, 89052
- Pfizer Investigational Site
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Las Vegas, Nevada, Stany Zjednoczone, 89128
- Pfizer Investigational Site
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Las Vegas, Nevada, Stany Zjednoczone, 89148
- Pfizer Investigational Site
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Las Vegas, Nevada, Stany Zjednoczone, 89135
- Pfizer Investigational Site
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Las Vegas, Nevada, Stany Zjednoczone, 89169
- Pfizer Investigational Site
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New Jersey
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Hackensack, New Jersey, Stany Zjednoczone, 07601
- Pfizer Investigational Site
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New Mexico
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Albuquerque, New Mexico, Stany Zjednoczone, 87131-0001
- Pfizer Investigational Site
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Farmington, New Mexico, Stany Zjednoczone, 87401-5631
- Pfizer Investigational Site
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New York
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Albany, New York, Stany Zjednoczone, 12206
- Pfizer Investigational Site
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Albany, New York, Stany Zjednoczone, 12208
- Pfizer Investigational Site
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Amsterdam, New York, Stany Zjednoczone, 12010
- Pfizer Investigational Site
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Brockport, New York, Stany Zjednoczone, 14420
- Pfizer Investigational Site
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Canadaigua, New York, Stany Zjednoczone, 14424
- Pfizer Investigational Site
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Geneva, New York, Stany Zjednoczone, 14456
- Pfizer Investigational Site
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Hudson, New York, Stany Zjednoczone, 12534
- Pfizer Investigational Site
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Latham, New York, Stany Zjednoczone, 12110
- Pfizer Investigational Site
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New York, New York, Stany Zjednoczone, 10021
- Pfizer Investigational Site
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New York, New York, Stany Zjednoczone, 10032
- Pfizer Investigational Site
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New York, New York, Stany Zjednoczone, 10022
- Pfizer Investigational Site
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Rexford, New York, Stany Zjednoczone, 12148
- Pfizer Investigational Site
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Rochester, New York, Stany Zjednoczone, 14623
- Pfizer Investigational Site
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Rochester, New York, Stany Zjednoczone, 14626
- Pfizer Investigational Site
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Troy, New York, Stany Zjednoczone, 12180
- Pfizer Investigational Site
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North Carolina
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Cary, North Carolina, Stany Zjednoczone, 27518
- Pfizer Investigational Site
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Clinton, North Carolina, Stany Zjednoczone, 28328
- Pfizer Investigational Site
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Elizabeth City, North Carolina, Stany Zjednoczone, 27909
- Pfizer Investigational Site
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Goldsboro, North Carolina, Stany Zjednoczone, 27534
- Pfizer Investigational Site
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Hickory, North Carolina, Stany Zjednoczone, 28602
- Pfizer Investigational Site
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Raleigh, North Carolina, Stany Zjednoczone, 27607
- Pfizer Investigational Site
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Raleigh, North Carolina, Stany Zjednoczone, 27614
- Pfizer Investigational Site
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Wilson, North Carolina, Stany Zjednoczone, 27893
- Pfizer Investigational Site
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Ohio
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Canton, Ohio, Stany Zjednoczone, 44718
- Pfizer Investigational Site
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Columbus, Ohio, Stany Zjednoczone, 43219
- Pfizer Investigational Site
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Oklahoma
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Norman, Oklahoma, Stany Zjednoczone, 73071
- Pfizer Investigational Site
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Oklahoma City, Oklahoma, Stany Zjednoczone, 73120
- Pfizer Investigational Site
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Oklahoma City, Oklahoma, Stany Zjednoczone, 73102
- Pfizer Investigational Site
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Oklahoma City, Oklahoma, Stany Zjednoczone, 73109
- Pfizer Investigational Site
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Oklahoma City, Oklahoma, Stany Zjednoczone, 73112-4416
- Pfizer Investigational Site
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Tulsa, Oklahoma, Stany Zjednoczone, 74133
- Pfizer Investigational Site
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Tulsa, Oklahoma, Stany Zjednoczone, 74104
- Pfizer Investigational Site
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Tulsa, Oklahoma, Stany Zjednoczone, 74136-1902
- Pfizer Investigational Site
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Oregon
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Eugene, Oregon, Stany Zjednoczone, 97401
- Pfizer Investigational Site
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Springfield, Oregon, Stany Zjednoczone, 97477
- Pfizer Investigational Site
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Pennsylvania
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Dunmore, Pennsylvania, Stany Zjednoczone, 18512-3169
- Pfizer Investigational Site
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Lemoyne, Pennsylvania, Stany Zjednoczone, 17043-1440
- Pfizer Investigational Site
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Philadelphia, Pennsylvania, Stany Zjednoczone, 19111-2497
- Pfizer Investigational Site
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Scranton, Pennsylvania, Stany Zjednoczone, 18508
- Pfizer Investigational Site
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South Carolina
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Easley, South Carolina, Stany Zjednoczone, 29640
- Pfizer Investigational Site
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Greenville, South Carolina, Stany Zjednoczone, 29615
- Pfizer Investigational Site
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Greenville, South Carolina, Stany Zjednoczone, 29605
- Pfizer Investigational Site
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Seneca, South Carolina, Stany Zjednoczone, 29672
- Pfizer Investigational Site
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Spartanburg, South Carolina, Stany Zjednoczone, 29307
- Pfizer Investigational Site
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Texas
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Austin, Texas, Stany Zjednoczone, 78705
- Pfizer Investigational Site
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Austin, Texas, Stany Zjednoczone, 78745
- Pfizer Investigational Site
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Austin, Texas, Stany Zjednoczone, 78759
- Pfizer Investigational Site
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Austin, Texas, Stany Zjednoczone, 78731
- Pfizer Investigational Site
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Austin, Texas, Stany Zjednoczone, 78758
- Pfizer Investigational Site
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Bedford, Texas, Stany Zjednoczone, 76022
- Pfizer Investigational Site
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Corpus Christi, Texas, Stany Zjednoczone, 78463
- Pfizer Investigational Site
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Dallas, Texas, Stany Zjednoczone, 75230
- Pfizer Investigational Site
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Dallas, Texas, Stany Zjednoczone, 75246
- Pfizer Investigational Site
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Fort Worth, Texas, Stany Zjednoczone, 76177
- Pfizer Investigational Site
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Georgetown, Texas, Stany Zjednoczone, 78626
- Pfizer Investigational Site
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Round Rock, Texas, Stany Zjednoczone, 78681
- Pfizer Investigational Site
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San Antonio, Texas, Stany Zjednoczone, 78229
- Pfizer Investigational Site
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San Antonio, Texas, Stany Zjednoczone, 78207
- Pfizer Investigational Site
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San Antonio, Texas, Stany Zjednoczone, 78217
- Pfizer Investigational Site
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San Antonio, Texas, Stany Zjednoczone, 78258
- Pfizer Investigational Site
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Tyler, Texas, Stany Zjednoczone, 75702
- Pfizer Investigational Site
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Webster, Texas, Stany Zjednoczone, 77598
- Pfizer Investigational Site
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Utah
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Salt Lake City, Utah, Stany Zjednoczone, 84112
- Pfizer Investigational Site
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Virginia
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Chesapeake, Virginia, Stany Zjednoczone, 23320
- Pfizer Investigational Site
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Hampton, Virginia, Stany Zjednoczone, 23666
- Pfizer Investigational Site
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Newport News, Virginia, Stany Zjednoczone, 23601
- Pfizer Investigational Site
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Newport News, Virginia, Stany Zjednoczone, 23502
- Pfizer Investigational Site
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Norfolk, Virginia, Stany Zjednoczone, 23502
- Pfizer Investigational Site
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Virginia Beach, Virginia, Stany Zjednoczone, 23456
- Pfizer Investigational Site
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Williamsburg, Virginia, Stany Zjednoczone, 23188
- Pfizer Investigational Site
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Washington
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Seattle, Washington, Stany Zjednoczone, 98195
- Pfizer Investigational Site
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Seattle, Washington, Stany Zjednoczone, 98109
- Pfizer Investigational Site
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West Virginia
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Morgantown, West Virginia, Stany Zjednoczone, 26506
- Pfizer Investigational Site
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Wisconsin
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Madison, Wisconsin, Stany Zjednoczone, 53792
- Pfizer Investigational Site
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Advanced renal cell carcinoma of clear cell origin or a component of clear cell histology.
- Measurable disease
Exclusion Criteria:
- Prior systemic therapy of any kind for advanced renal cell cancer
- History of brain metastases
- Uncontrolled hypertension
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: A
|
Sunitinib malate starting dose 50 mg per day for four weeks, followed by a two week off-drug period.
This six week cycle is repeated.
|
|
Eksperymentalny: C
|
Sunitinib malate starting dose 37.5 mg daily continuous daily regimen.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Time to Tumor Progression (TTP) Assessed Using Memorial Sloan-Kettering Cancer Center (MSKCC) Prognostic Factors Model
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
MSKCC Prognostic Factor Model assessed as low(0),intermediate(1-2) or high(=>3) based on number of criteria present such as Karnofsky performance status < 80 %, Lactate dehydrogenase > 1.5 * Upper limit of Normal,Hemoglobin < lower limit of normal, serum calcium > 10 mg/dL;Time from first diagnosis of renal cell carcinoma to start of systemic therapy of < 1 year.TTP was time from start of study treatment to first documentation of objective tumor progression or death due to cancer.TTP was calculated as (first event date minus date of first dose of study medication plus 1) divided by 30.44.
|
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Percentage of Participants With Objective Response (OR)
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
Percentage of participants with objective response based assessment of confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST).
Confirmed responses are those that persist on repeat imaging study at least 4 weeks after initial documentation of response.
CR are defined as the disappearance of all lesions (target and/or non target).
PR are those with atleast 30% decrease in the sum of the longest dimensions of the target lesions taking as a reference the baseline sum longest dimensions.
|
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
|
Duration of Response (DR)
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
Time from the first documentation of objective tumor response to objective tumor progression or death due to any cause.
Duration of tumor response was calculated as (the date of the first documentation of objective tumor progression or death due to cancer minus the date of the first CR or PR that was subsequently confirmed plus 1) divided by 30.44.
DR was calculated for the subgroup of participants with a confirmed objective tumor response.
|
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
|
Overall Survival (OS) Assessed Using MSKCC Prognostic Factors Model
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
MSKCC Prognostic Factor Model assessed as low (0), intermediate (1-2) or high (=>3) based upon number of criteria present.
Criteria as follows: Karnofsky performance status < 80 %, Lactate dehydrogenase > 1.5 * Upper limit of Normal, Hemoglobin < lower limit of normal for local lab, Corrected serum calcium > 10 mg/dL; Time from first diagnosis of renal cell carcinoma to start of systemic therapy of < 1 year.
OS was defined as time from date of start of treatment to date of death due to any cause.
OS, in months, was calculated as (event date -start of treatment date + 1)/30.44.
|
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Functional Assessment of Cancer Therapy-General (FACT-G)
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
FACT-G is core questionnaire of Functional Assessment of Chronic Illness Therapy (FACIT) measurement system to evaluate quality of life (QoL) in cancer population.FACT-G consisted of 27 questions grouped in 4 domains of general Health-Related QoL(HRQoL):Physical Well-being(PWB),Social/Family Well-Being (SWB),Emotional Well-Being (EWB) and Functional Well-Being (FWB);each ranging from 0 (not at all) to 4 (very much) so that FACT-G ranged between 0-108.Since questions could be reversed coded, as appropriate, before calculating FACT-G,0 and 108 could be considered worst and best health states.
|
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
|
FACT-Kidney Symptom Index for Disease Related Symptoms (FKSI-DRS)
Ramy czasowe: From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
FKSI-DRS is a subset of FKSI which is a questionnaire for Functional Assessment of Cancer Therapy -Kidney Symptom Index used to assess QoL/participant-reported outcomes for participants diagnosed with renal cell cancer. The FKSI contained 15 questions and the FKSI-DRS consisted of 9 questions each ranging from 0 (not at all) to 4 (very much) so that FKSI-DRS ranged between 0-36. Since the questions could be reversed coded, as appropriate, before calculating FKSI-DRS, 0 and 36 could be considered the worst and best health states based on the 9 questions comprising FKSI-DRS. |
From date of randomization until the date of first documented progression or date of death due to any cause, assessed up to a maximum of 2 years
|
Współpracownicy i badacze
Sponsor
Publikacje i pomocne linki
Publikacje ogólne
- de Velasco G, McKay RR, Lin X, Moreira RB, Simantov R, Choueiri TK. Comprehensive Analysis of Survival Outcomes in Non-Clear Cell Renal Cell Carcinoma Patients Treated in Clinical Trials. Clin Genitourin Cancer. 2017 Dec;15(6):652-660.e1. doi: 10.1016/j.clgc.2017.03.004. Epub 2017 Mar 21.
- Grunwald V, Lin X, Kalanovic D, Simantov R. Early Tumour Shrinkage: A Tool for the Detection of Early Clinical Activity in Metastatic Renal Cell Carcinoma. Eur Urol. 2016 Dec;70(6):1006-1015. doi: 10.1016/j.eururo.2016.05.010. Epub 2016 May 26.
- Grunwald V, McKay RR, Krajewski KM, Kalanovic D, Lin X, Perkins JJ, Simantov R, Choueiri TK. Depth of remission is a prognostic factor for survival in patients with metastatic renal cell carcinoma. Eur Urol. 2015 May;67(5):952-8. doi: 10.1016/j.eururo.2014.12.036. Epub 2015 Jan 7.
- Motzer RJ, Hutson TE, Hudes GR, Figlin RA, Martini JF, English PA, Huang X, Valota O, Williams JA. Investigation of novel circulating proteins, germ line single-nucleotide polymorphisms, and molecular tumor markers as potential efficacy biomarkers of first-line sunitinib therapy for advanced renal cell carcinoma. Cancer Chemother Pharmacol. 2014 Oct;74(4):739-50. doi: 10.1007/s00280-014-2539-0. Epub 2014 Aug 7.
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Nowotwory według typu histologicznego
- Nowotwory
- Nowotwory urologiczne
- Nowotwory układu moczowo-płciowego
- Nowotwory według lokalizacji
- Choroby nerek
- Choroby Urologiczne
- Rak gruczołowy
- Rak
- Nowotwory gruczołowe i nabłonkowe
- Nowotwory nerek
- Rak, Komórka Nerki
- Fizjologiczne skutki leków
- Molekularne mechanizmy działania farmakologicznego
- Inhibitory enzymów
- Środki przeciwnowotworowe
- Inhibitory angiogenezy
- Środki modulujące angiogenezę
- Substancje wzrostowe
- Inhibitory wzrostu
- Inhibitory kinazy białkowej
- Sunitynib
Inne numery identyfikacyjne badania
- A6181065
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