- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT01196091
A Study of LY2127399 in Participants With Systemic Lupus Erythematosus
A Phase 3, Multicenter, Randomized, Double Blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Subcutaneous LY2127399 in Participants With Systemic Lupus Erythematosus (SLE)
Przegląd badań
Status
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 3
Kontakty i lokalizacje
Lokalizacje studiów
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Buenos Aires, Argentyna, C1417EYG
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Caba, Argentyna, C1181ACH
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Córdoba, Argentyna, X5016KEH
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Rosario, Argentyna, S2000PBJ
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San Juan, Argentyna, 5400
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Tucuman, Argentyna, 4000
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Graz, Austria, 8036
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Vienna, Austria, A1090
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Brest, Białoruś, 224027
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Grodno, Białoruś, 230017
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Minsk, Białoruś, 220116
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Plovdiv, Bułgaria, 4002
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Sofia, Bułgaria, 1612
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Stara Zagora, Bułgaria, 6003
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Varna, Bułgaria, 9010
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Osorno, Chile, 5290000
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Santiago, Chile, 7500000
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Valdivia, Chile
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Osijek, Chorwacja, 31000
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Al Minya, Egipt, 61111
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Alexandria, Egipt, 21131
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Cairo, Egipt, 941400
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Angeles City, Filipiny, 2009
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Cebu, Filipiny, 6000
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Davao City, Filipiny, 8000
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Ermita, Filipiny, 1000
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Espana, Filipiny, 1008
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Iloilo City, Filipiny, 5000
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Manila, Filipiny, 1007
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Paranaque, Filipiny
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Quezon City, Filipiny, 1102
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Guatemala, Gwatemala, 1010
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Aichi, Japonia, 4600001
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Chiba, Japonia, 284-0003
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Fukuoka, Japonia, 807-8556
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Hokkaido, Japonia, 060-8648
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Japan, Japonia, 852-8501
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Miyagi, Japonia, 980-8574
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Nagasaki, Japonia, 856-8562
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Osaka, Japonia, 530-8480
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Tokyo, Japonia, 101-0062
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British Columbia
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Kelowna, British Columbia, Kanada, V1Y3G5
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Ontario
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Markham, Ontario, Kanada, L3P1A8
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Newmarket, Ontario, Kanada, L3Y3R7
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Bogota, Kolumbia
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Bucaramanga, Kolumbia, 681001
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Cali, Kolumbia
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Chia, Kolumbia
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Medellín, Kolumbia, 574
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Bitola, Macedonia, była jugosłowiańska republika, 7000
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Skopje, Macedonia, była jugosłowiańska republika, 1000
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Stip, Macedonia, była jugosłowiańska republika, 2000
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Bad Nauheim, Niemcy, 61231
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Baden-Baden, Niemcy, 76530
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Berlin, Niemcy, 14059
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Erlangen, Niemcy, 91054
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Freiburg, Niemcy, 79106
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Hildesheim, Niemcy, 31134
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Jena, Niemcy, 07747
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Zerbst, Niemcy, 39261
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Arequipa, Peru
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Lima, Peru, L41
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Lince, Peru, Lima14
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Piura, Peru
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?Ód?, Polska, 94-017
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Bytom, Polska, 41-902
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Poznan, Polska, 61-397
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Sosnowiec, Polska, 41-200
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Warsaw, Polska, 02-507
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Wroc?Aw, Polska, 50-368
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San Juan, Portoryko, 00918
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Santurce, Portoryko, 00909
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Bucheon, Republika Korei, 420-717
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Daegu, Republika Korei, 700-712
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Daejeon, Republika Korei, 301-721
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Gwangju, Republika Korei, 501-757
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Incheon, Republika Korei, 405-760
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Jeonju-Si, Republika Korei, 561712
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Seoul, Republika Korei, 143-729
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Suwon, Republika Korei, 443-721
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Singapore, Singapur, 258499
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Alabama
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Birmingham, Alabama, Stany Zjednoczone, 35294
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Arizona
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Glendale, Arizona, Stany Zjednoczone, 85304
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Mesa, Arizona, Stany Zjednoczone, 85202
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Paradise Valley, Arizona, Stany Zjednoczone, 85253
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Peoria, Arizona, Stany Zjednoczone, 85381
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Phoenix, Arizona, Stany Zjednoczone, 85037
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Arkansas
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Little Rock, Arkansas, Stany Zjednoczone, 72205
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California
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Anaheim, California, Stany Zjednoczone, 92805
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Glendale, California, Stany Zjednoczone, 91204
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lakewood, California, Stany Zjednoczone, 90712
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Long Beach, California, Stany Zjednoczone, 90808
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Los Angeles, California, Stany Zjednoczone, 90048
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sacramento, California, Stany Zjednoczone, 95825
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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San Leandro, California, Stany Zjednoczone, 94578
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Upland, California, Stany Zjednoczone, 91786
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Connecticut
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Danbury, Connecticut, Stany Zjednoczone, 06810
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Farmington, Connecticut, Stany Zjednoczone, 06030
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Norwich, Connecticut, Stany Zjednoczone, 06360
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Trumbull, Connecticut, Stany Zjednoczone, 06611
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Florida
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Boca Raton, Florida, Stany Zjednoczone, 33486
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Clearwater, Florida, Stany Zjednoczone, 33765
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Doral, Florida, Stany Zjednoczone, 33166
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Fort Lauderdale, Florida, Stany Zjednoczone, 33334
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Jacksonville, Florida, Stany Zjednoczone, 32216
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lake Mary, Florida, Stany Zjednoczone, 32746
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Miami, Florida, Stany Zjednoczone, 33169
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Orange Park, Florida, Stany Zjednoczone, 32073
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Palm Harbor, Florida, Stany Zjednoczone, 34684
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Saint Petersburg, Florida, Stany Zjednoczone, 33710
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tamarac, Florida, Stany Zjednoczone, 33321
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Tampa, Florida, Stany Zjednoczone, 33612
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Georgia
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Atlanta, Georgia, Stany Zjednoczone, 30342
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Decatur, Georgia, Stany Zjednoczone, 30033
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Marietta, Georgia, Stany Zjednoczone, 30060
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Idaho
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Boise, Idaho, Stany Zjednoczone, 83702
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Illinois
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Chicago, Illinois, Stany Zjednoczone, 60612
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Peoria, Illinois, Stany Zjednoczone, 61636
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Indiana
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Muncie, Indiana, Stany Zjednoczone, 47304
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kansas
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Kansas City, Kansas, Stany Zjednoczone, 66160
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kentucky
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Bowling Green, Kentucky, Stany Zjednoczone, 42101
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lexington, Kentucky, Stany Zjednoczone, 40504
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Maryland
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Baltimore, Maryland, Stany Zjednoczone, 21239
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Hagerstown, Maryland, Stany Zjednoczone, 21742
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wheaton, Maryland, Stany Zjednoczone, 20902
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Michigan
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Grand Rapids, Michigan, Stany Zjednoczone, 49546
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Minnesota
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Eagan, Minnesota, Stany Zjednoczone, 55121
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Missouri
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Florissant, Missouri, Stany Zjednoczone, 63031
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Nebraska
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Lincoln, Nebraska, Stany Zjednoczone, 68516
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Omaha, Nebraska, Stany Zjednoczone, 68134
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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New Jersey
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Clifton, New Jersey, Stany Zjednoczone, 07012
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Teaneck, New Jersey, Stany Zjednoczone, 07666
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Toms River, New Jersey, Stany Zjednoczone, 08755
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Mexico
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Albuquerque, New Mexico, Stany Zjednoczone, 87102
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New York
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Bronx, New York, Stany Zjednoczone, 10457
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Endwell, New York, Stany Zjednoczone, 13760
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Manhasset, New York, Stany Zjednoczone, 11030
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
New York, New York, Stany Zjednoczone, 10019
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Rochester, New York, Stany Zjednoczone, 14618
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Carolina
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Charlotte, North Carolina, Stany Zjednoczone, 28210
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greenville, North Carolina, Stany Zjednoczone, 27834
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Hickory, North Carolina, Stany Zjednoczone, 28602
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Ohio
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Cincinnati, Ohio, Stany Zjednoczone, 45229
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Middleburg Heights, Ohio, Stany Zjednoczone, 44130
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Oklahoma
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Edmond, Oklahoma, Stany Zjednoczone, 73013
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Oklahoma City, Oklahoma, Stany Zjednoczone, 73103
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Pennsylvania
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Philadelphia, Pennsylvania, Stany Zjednoczone, 19107
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pittsburgh, Pennsylvania, Stany Zjednoczone, 15217
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Willow Grove, Pennsylvania, Stany Zjednoczone, 19090
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Carolina
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Columbia, South Carolina, Stany Zjednoczone, 29204
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greenville, South Carolina, Stany Zjednoczone, 29601
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
North Charleston, South Carolina, Stany Zjednoczone, 29406
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Tennessee
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Crossville, Tennessee, Stany Zjednoczone, 38555
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Hixon, Tennessee, Stany Zjednoczone, 37343
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Jackson, Tennessee, Stany Zjednoczone, 38305
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Texas
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Allen, Texas, Stany Zjednoczone, 75013
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Dallas, Texas, Stany Zjednoczone, 75390
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Houston, Texas, Stany Zjednoczone, 77034
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Irving, Texas, Stany Zjednoczone, 75061
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Mesquite, Texas, Stany Zjednoczone, 75150
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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San Antonio, Texas, Stany Zjednoczone, 78229
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sugar Land, Texas, Stany Zjednoczone, 77478
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Waco, Texas, Stany Zjednoczone, 76708
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Virginia
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Chesapeake, Virginia, Stany Zjednoczone, 23320
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Danville, Virginia, Stany Zjednoczone, 24541
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Richmond, Virginia, Stany Zjednoczone, 23294
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Williamsburg, Virginia, Stany Zjednoczone, 23185
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Washington
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Tacoma, Washington, Stany Zjednoczone, 98405
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wisconsin
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Milwaukee, Wisconsin, Stany Zjednoczone, 53226
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bangkok, Tajlandia, 10700
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Chiang Mai, Tajlandia, 50200
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Donetsk, Ukraina, 83001
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Ivano-Frankivsk, Ukraina, 76008
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kharkiv, Ukraina, 61029
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kryvyi Rih, Ukraina, 50056
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kyiv, Ukraina, 1601
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lviv, Ukraina, 79011
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Odesa, Ukraina, 65025
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Simferopol, Ukraina, 95017
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Ternopil, Ukraina, 46002
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Uzhorod, Ukraina, 88018
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Vinnytsya, Ukraina, 21018
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Zaporizhzhia, Ukraina, 69600
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Zhytomyr, Ukraina, 10002
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Brescia, Włochy, 25123
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Genova, Włochy, 16132
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Milano, Włochy, 20122
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Napoli, Włochy, 80131
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Padova, Włochy, 35128
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Palermo, Włochy, 90127
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Scafati, Włochy, 84018
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Torino, Włochy, 10128
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Clinical diagnosis of SLE by American College of Rheumatology (ACR) criteria
- Have positive antinuclear antibodies (ANA)
- Agree not to become pregnant throughout the course of the trial
- Have a screening SELENA-SLEDAI score ≥6. (The participant must be actively exhibiting all the symptoms scored on the screening SELENA-SLEDAI on the day of screening.)
Exclusion Criteria:
- Have active severe Lupus kidney disease
- Have active Central Nervous System or peripheral neurologic disease
- Have received intravenous immunoglobulin (IVIg) within 180 days of randomization
- Have active or recent infection within 30 days of screening
- Have had a serious infection within 90 days of randomization
- Have evidence or test positive for Hepatitis B
- Have Hepatitis C
- Are human immunodeficiency virus (HIV) positive
- Have evidence of active or latent tuberculosis (TB)
- Presence of significant laboratory abnormalities at screening
- Have had a malignancy in the past 5 years, except for cervical carcinoma in-situ or basal cell or squamous epithelial skin cell that were completely resected with no reoccurrence in the 3 yrs prior to randomization
- Have received greater than 40 mgs of prednisone or equivalent in the past 30 days
- Have changed your dose of antimalarial drug in the past 30 days
- Have changed your dose of immunosuppressive drug in the past 90 days
- Have previously received rituximab
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Komparator placebo: Placebo
Administrowany SC
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Inne nazwy:
Administered via subcutaneous injection for 52 weeks.
A matching loading dose of corticosteroids, NSAIDs, antimalarials, or immunosuppressants will also be administered at the first dose
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Eksperymentalny: LY2127399 every 2 weeks
Administered SC
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120 mg administered via subcutaneous (SC) injection for 52 weeks.
240 mg loading dose will be administered as the first dose of study drug.
Inne nazwy:
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Eksperymentalny: LY2127399 every 4 wks
During the Treatment Period, for blinding purposes, patients will alternate injections of LY2127399 and injections of placebo every 2 weeks.
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120 mg administered via subcutaneous (SC) injection for 52 weeks.
240 mg loading dose will be administered as the first dose of study drug.
Inne nazwy:
Podawany we wstrzyknięciu podskórnym przez 52 tygodnie.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Odsetek uczestników, u których uzyskano odpowiedź na leczenie SLE w 52. tygodniu
Ramy czasowe: 52 tygodnie
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Odsetek uczestników ze zmniejszeniem wyniku SELENA SLEDAI o ≥ 5 punktów w stosunku do wartości wyjściowej i bez pogorszenia (wzrost < 0,30 punktu w stosunku do wartości początkowej) w PGA i bez nowej punktacji BILAG A w dziedzinie narządów lub 2 nowych punktacji BILAG B w dziedzinie narządów w porównaniu z wartościami wyjściowymi . SELENA SLEDAI jest obliczana na podstawie 24 indywidualnych deskryptorów w 9 układach narządów; 0 oznacza nieaktywną chorobę, a maksymalny teoretyczny wynik to 105; wyniki > 20 są rzadkie. PGA to wizualna skala analogowa, punktowana od 0 do 3 (0=brak, 1=łagodne, 2=umiarkowane, 3=ciężkie). BILAG wykorzystuje pojedynczą punktację dla każdej z 9 domen narządowych; waha się od ciężkiego (A) do braku choroby (E). Uczestnicy, którzy nie byli w stanie spełnić wymagań dotyczących dozwolonych leków towarzyszących, zostali uznani za niereagujących, podobnie jak uczestnicy, którzy odpadli lub brakowało im danych z 52. tygodnia. |
52 tygodnie
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Percentage Participants Able to Decrease Dose of Prednisone or Equivalent With No Increase in Disease Activity at Week 52
Ramy czasowe: 52 weeks
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A participant achieves corticosteroid sparing effects (quiescent disease) if they have met the following criteria during Weeks 24 through 52; able to decrease their dose of prednisone or equivalent to 7.5 mg/day or less, have quiescent disease (BILAG C score or better in all nine systems), and no BILAG A or B flares in the previous three months, without an increase in either antimalarials or immunosuppressants on or prior to the visit.
Only participants receiving a prednisone or equivalent dose of more than 7.5 mg/day at baseline are included.
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52 weeks
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Zmiana od wartości początkowej do 52 tygodni poziomu anty-dwuniciowego kwasu dezoksyrybonukleinowego (anty-dsDNA)
Ramy czasowe: Wartość wyjściowa, 52 tygodnie
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Anty-dwuniciowy kwas dezoksyrybonukleinowy (anty-dsDNA) jest analitem laboratoryjnym używanym do wspomagania diagnozy SLE.
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Wartość wyjściowa, 52 tygodnie
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Zmiana od punktu początkowego do punktu końcowego w 52. tygodniu w wyniku wskaźnika aktywności choroby tocznia rumieniowatego układowego (SLEDAI2K)
Ramy czasowe: Wartość wyjściowa, 52 tygodnie
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Wynik Indeksu Aktywności Choroby SLE 2000 (SLEDAI-2K) jest ważonym, zbiorczym wskaźnikiem aktywności choroby tocznia.
SLEDAI-2K oblicza się na podstawie 24 indywidualnych deskryptorów w 9 układach narządów; 0 oznacza nieaktywną chorobę, a maksymalny teoretyczny wynik to 105.
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Wartość wyjściowa, 52 tygodnie
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Czas do pierwszego ostrego zaostrzenia SLE (SFI)
Ramy czasowe: Linia bazowa do 52 tygodni
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SFI wykorzystuje punktację wskaźnika aktywności choroby SELENA-SLEDAI, scenariusze aktywności choroby, zmiany leczenia i PGA do określenia łagodnych/umiarkowanych i ciężkich zaostrzeń. Indeks uwzględnia bezwzględną zmianę w całkowitych wynikach, nowe lub nasilające się objawy oraz wzrost stosowania kortykosteroidów lub hospitalizacji z powodu aktywności choroby. Czas do pierwszego ciężkiego zaostrzenia SLE (SFI) (w dniach) oblicza się w następujący sposób: (data rozpoczęcia pierwszego ciężkiego zaostrzenia SLE (SFI) — data randomizacji + 1). |
Linia bazowa do 52 tygodni
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Percentage of Participants With No Worsening in Physician Global Assessment (PGA) Score at 52 Weeks
Ramy czasowe: 52 weeks
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Physician's Global Assessment (PGA) is a single-item clinician rated assessment of the patient's current level of disease activity measured on a continuous 100 millimeter (mm) visual analytic scale with benchmarks of 0, 1, 2, and 3 from left to right corresponding to no, mild, moderate, and severe SLE disease activity.
Scores are presented from 0 to 100.
No worsening is defined as increase of ≥0.3 points.
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52 weeks
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Zmiana od punktu początkowego do 52-tygodniowego punktu końcowego w wynikach inwentarza krótkiego zmęczenia (BFI).
Ramy czasowe: Wartość wyjściowa, 52 tygodnie
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Skala zgłaszana przez uczestników, która mierzy nasilenie zmęczenia na podstawie najgorszego zmęczenia odczuwanego w ciągu ostatnich 24 godzin.
Oceny nasilenia wahały się od 0 (brak zmęczenia) do 10 (zmęczenie tak poważne, jak tylko można sobie wyobrazić).
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Wartość wyjściowa, 52 tygodnie
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Change From Baseline to 52 Week Endpoint Lupus Quality of Life (LupusQoL) Domain Scores
Ramy czasowe: Baseline, 52 weeks
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The LupusQoL is a disease-specific, 34-item, self-report questionnaire designed to measure the health-related quality of life (HRQoL) of participants with SLE within 8 domains.Responses are based on a 5-point Likert scale where 0 (all of the time) to 4 (never).
A LupusQoL score for each domain is reported on a 0 to 100 scale, with greater values indicating better HRQoL.
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Baseline, 52 weeks
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Czas do pierwszej nowej Grupy Oceny Tocznia z Wysp Brytyjskich (BILAG A) lub 2 nowych zaostrzeń BILAG B SLE
Ramy czasowe: Linia bazowa do 52 tygodni
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Instrument British Isles Lupus Assessment Group (BILAG) ocenia globalną aktywność choroby w 9 domenach układów narządów. Zaostrzenie BILAG jest oceniane dla każdej z 9 domen narządowych przy użyciu zasad wskaźnika zaostrzenia BILAG2004; A to ostry zaostrzenie, a B to umiarkowany zaostrzenie. Czas do pierwszego rozbłysku BILAG A lub dwóch rozbłysków BILAG B (w dniach) oblicza się w następujący sposób: (Data rozpoczęcia pierwszego rozbłysku BILAG A lub dwóch rozbłysków BILAG B - Data randomizacji + 1). Dwa rozbłyski BILAG B muszą wystąpić w różnych domenach podczas tej samej wizyty. |
Linia bazowa do 52 tygodni
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Change From Baseline to 52 Week Endpoint in PGA
Ramy czasowe: Baseline, 52 weeks
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Physician's Global Assessment (PGA) is a single-item clinician rated assessment of the patient's current level of disease activity measured on a continuous 100-mm visual analytic scale with benchmarks of 0, 1, 2, and 3 from left to right corresponding to no, mild, moderate, and severe SLE disease activity.
Scores range from 0, being worst possible to 100 being very active or best possible.
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Baseline, 52 weeks
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Odsetek uczestników ze wzrostem dawki kortykosteroidów po 52 tygodniach
Ramy czasowe: 52 tygodnie
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Zwiększenie dawki kortykosteroidów podczas wizyty zdefiniowano jako zmianę w stosunku do wartości wyjściowej o więcej niż 2,5 mg/dobę dawki prednizonu lub równoważnego przy zastosowaniu średniej dziennej dawki kortykosteroidów przyjmowanej od poprzedniej zaplanowanej wizyty.
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52 tygodnie
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Zmiana od punktu początkowego do punktu końcowego po 52 tygodniach w skali aktywności choroby SELENA-SLEDAI
Ramy czasowe: Wartość wyjściowa, 52 tygodnie
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Bezpieczeństwo estrogenów w Krajowej Ocenie Tocznia Rumieniowatego - Wynik Indeksu Aktywności Choroby SLE (SELENA-SLEDAI) jest ważonym, łącznym wskaźnikiem aktywności choroby tocznia.
SELENA-SLEDAI jest obliczana na podstawie 24 indywidualnych deskryptorów w 9 układach narządów; 0 oznacza nieaktywną chorobę, a maksymalny teoretyczny wynik to 105.
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Wartość wyjściowa, 52 tygodnie
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Percentage of Participants Achieving a Response as Measured by Modified SRI With No BILAG A or No More Than 1 BILAG B Organ Domain Flares at 52 Weeks
Ramy czasowe: 52 weeks
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Percentage of participants with a ≥ 5 point reduction from baseline in SELENA SLEDAI score, and no worsening (increase of < 0.30 points from baseline) in PGA, and no new BILAG A or no more than 1 new BILAG B organ domain flare compared with baseline. (Primary outcome modified to use BILAG flare instead of BILAG disease score) SELENA SLEDAI is calculated from 24 individual descriptors across 9 organ systems; 0 indicates inactive disease and the maximum theoretical score is 105. PGA is a visual analog scale scored from 0 to 3 (0=none, 1=mild, 2=moderate, 3=severe). BILAG flare is assessed for each of the 9 organ domains; A is a severe flare and B is a moderate flare. Patients who were unable to comply with allowed concomitant medications requirements were considered non-responders, as were participants who dropped out or were missing Week 52 data. |
52 weeks
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Number of Participants With No New BILAG A and No More Than One New BILAG B Disease Activity Scores Compared to Baseline
Ramy czasowe: Baseline through 52 weeks
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The BILAG2004 index is a validated global disease activity index designed on the basis of the physician's ITT, focusing on changes in disease manifestations (new, improved, worsening, etc) occurring in the last 4 weeks compared with the previous 4 weeks. The instrument assesses 97 clinical signs, symptoms, and laboratory parameters across 9 organ system domains: constitutional, mucocutaneous, neuropsychiatric, musculoskeletal, cardiorespiratory, gastrointestinal, opthalmic, renal and hematology. |
Baseline through 52 weeks
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Współpracownicy i badacze
Sponsor
Publikacje i pomocne linki
Publikacje ogólne
- Toro-Dominguez D, Martorell-Marugan J, Martinez-Bueno M, Lopez-Dominguez R, Carnero-Montoro E, Barturen G, Goldman D, Petri M, Carmona-Saez P, Alarcon-Riquelme ME. Scoring personalized molecular portraits identify Systemic Lupus Erythematosus subtypes and predict individualized drug responses, symptomatology and disease progression. Brief Bioinform. 2022 Sep 20;23(5):bbac332. doi: 10.1093/bib/bbac332.
- Li Y, Higgs RE, Hoffman RW, Dow ER, Liu X, Petri M, Wallace DJ, Dorner T, Eastwood BJ, Miller BB, Liu Y. A Bayesian gene network reveals insight into the JAK-STAT pathway in systemic lupus erythematosus. PLoS One. 2019 Dec 2;14(12):e0225651. doi: 10.1371/journal.pone.0225651. eCollection 2019.
- Kalunian KC, Urowitz MB, Isenberg D, Merrill JT, Petri M, Furie RA, Morgan-Cox MA, Taha R, Watts S, Silk M, Linnik MD. Clinical trial parameters that influence outcomes in lupus trials that use the systemic lupus erythematosus responder index. Rheumatology (Oxford). 2018 Jan 1;57(1):125-133. doi: 10.1093/rheumatology/kex368.
- Rovin BH, Dooley MA, Radhakrishnan J, Ginzler EM, Forrester TD, Anderson PW. The impact of tabalumab on the kidney in systemic lupus erythematosus: results from two phase 3 randomized, clinical trials. Lupus. 2016 Dec;25(14):1597-1601. doi: 10.1177/0961203316650734. Epub 2016 May 24.
- Hoffman RW, Merrill JT, Alarcon-Riquelme MM, Petri M, Dow ER, Nantz E, Nisenbaum LK, Schroeder KM, Komocsar WJ, Perumal NB, Linnik MD, Airey DC, Liu Y, Rocha GV, Higgs RE. Gene Expression and Pharmacodynamic Changes in 1,760 Systemic Lupus Erythematosus Patients From Two Phase III Trials of BAFF Blockade With Tabalumab. Arthritis Rheumatol. 2017 Mar;69(3):643-654. doi: 10.1002/art.39950.
- Isenberg DA, Petri M, Kalunian K, Tanaka Y, Urowitz MB, Hoffman RW, Morgan-Cox M, Iikuni N, Silk M, Wallace DJ. Efficacy and safety of subcutaneous tabalumab in patients with systemic lupus erythematosus: results from ILLUMINATE-1, a 52-week, phase III, multicentre, randomised, double-blind, placebo-controlled study. Ann Rheum Dis. 2016 Feb;75(2):323-31. doi: 10.1136/annrheumdis-2015-207653. Epub 2015 Sep 3.
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 (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Choroby układu odpornościowego
- Toczeń rumieniowaty układowy
- Choroby tkanki łącznej
- Choroby Autoimmunologiczne
- Fizjologiczne skutki leków
- Środki przeciwinfekcyjne
- Agenty obwodowego układu nerwowego
- Środki przeciwbólowe
- Agenci systemu sensorycznego
- Środki przeciwbólowe, nie narkotyczne
- Środki przeciwreumatyczne
- Czynniki immunologiczne
- Środki przeciwpierwotniacze
- Środki przeciwpasożytnicze
- Środki przeciwzapalne
- Środki immunosupresyjne
- Środki przeciwzapalne, niesteroidowe
- Leki przeciwmalaryczne
Inne numery identyfikacyjne badania
- 13656
- H9B-MC -BCDS (Inny identyfikator: Eli Lilly and Company)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na LY2127399
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Eli Lilly and CompanyZakończonyReumatyzmArgentyna, Niemcy, Indie, Republika Korei, Stany Zjednoczone, Węgry, Tajwan, Bułgaria, Francja, Federacja Rosyjska, Hiszpania, Ukraina, Kolumbia, Meksyk, Polska, Japonia, Chorwacja, Grecja, Nowa Zelandia, Rumunia, Afryka Południowa i więcej
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Eli Lilly and CompanyZakończonyNiewydolność nerek, przewlekłaStany Zjednoczone
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Eli Lilly and CompanyZakończony
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Applied Molecular EvolutionEli Lilly and CompanyZakończonySzpiczak mnogiStany Zjednoczone
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Eli Lilly and CompanyZakończonyReumatyzmArgentyna, Indie, Stany Zjednoczone, Węgry, Bułgaria, Meksyk, Ukraina, Kolumbia, Tajwan, Polska, Japonia, Republika Korei, Nowa Zelandia, Rumunia, Afryka Południowa, Australia, Chorwacja, Litwa, Malezja, Federacja Rosyjska, Słow... i więcej
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Eli Lilly and CompanyZakończonyReumatyzmStany Zjednoczone, Niemcy, Tajwan, Francja, Japonia, Meksyk, Polska, Federacja Rosyjska, Hiszpania, Kolumbia, Argentyna, Grecja, Nowa Zelandia, Afryka Południowa, Australia, Republika Korei, Brazylia, Włochy, Malezja
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Eli Lilly and CompanyZakończonyToczeń rumieniowaty układowy | Choroby autoimmunologiczne | Choroba tkanki łącznejIndie, Stany Zjednoczone, Węgry, Rumunia, Hiszpania, Francja, Tajwan, Federacja Rosyjska, Zjednoczone Królestwo, Australia, Łotwa, Meksyk, Afryka Południowa, Kanada, Izrael, Brazylia, Serbia, Ekwador, Malezja, Nowa Zelandia, Tun...
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Eli Lilly and CompanyZakończonyToczeń rumieniowaty układowy | Choroby autoimmunologiczne | Choroba tkanki łącznejStany Zjednoczone
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Eli Lilly and CompanyZakończony
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Eli Lilly and CompanyZakończonyReumatyzmStany Zjednoczone, Meksyk, Węgry, Indie, Argentyna, Chile, Ukraina, Australia, Rumunia, Niemcy, Polska, Słowacja