- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus 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)
Tutkimuksen yleiskatsaus
Tila
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 3
Yhteystiedot ja paikat
Opiskelupaikat
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Buenos Aires, Argentiina, C1417EYG
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Caba, Argentiina, C1181ACH
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Córdoba, Argentiina, X5016KEH
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Rosario, Argentiina, S2000PBJ
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San Juan, Argentiina, 5400
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Tucuman, Argentiina, 4000
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Plovdiv, Bulgaria, 4002
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Sofia, Bulgaria, 1612
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Stara Zagora, Bulgaria, 6003
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Varna, Bulgaria, 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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Al Minya, Egypti, 61111
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Alexandria, Egypti, 21131
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Cairo, Egypti, 941400
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Angeles City, Filippiinit, 2009
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Cebu, Filippiinit, 6000
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Davao City, Filippiinit, 8000
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Ermita, Filippiinit, 1000
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Espana, Filippiinit, 1008
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Iloilo City, Filippiinit, 5000
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Manila, Filippiinit, 1007
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Paranaque, Filippiinit
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Quezon City, Filippiinit, 1102
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Guatemala, Guatemala, 1010
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Brescia, Italia, 25123
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Genova, Italia, 16132
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Milano, Italia, 20122
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Napoli, Italia, 80131
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Padova, Italia, 35128
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Palermo, Italia, 90127
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Scafati, Italia, 84018
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Torino, Italia, 10128
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Graz, Itävalta, 8036
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Vienna, Itävalta, A1090
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Aichi, Japani, 4600001
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Chiba, Japani, 284-0003
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Fukuoka, Japani, 807-8556
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Hokkaido, Japani, 060-8648
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Japan, Japani, 852-8501
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Miyagi, Japani, 980-8574
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Nagasaki, Japani, 856-8562
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Osaka, Japani, 530-8480
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Tokyo, Japani, 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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Bucheon, Korean tasavalta, 420-717
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Daegu, Korean tasavalta, 700-712
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Daejeon, Korean tasavalta, 301-721
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Gwangju, Korean tasavalta, 501-757
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Incheon, Korean tasavalta, 405-760
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Jeonju-Si, Korean tasavalta, 561712
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Seoul, Korean tasavalta, 143-729
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Suwon, Korean tasavalta, 443-721
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Osijek, Kroatia, 31000
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Bitola, Makedonia, entinen Jugoslavian tasavalta, 7000
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Skopje, Makedonia, entinen Jugoslavian tasavalta, 1000
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Stip, Makedonia, entinen Jugoslavian tasavalta, 2000
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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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San Juan, Puerto Rico, 00918
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Santurce, Puerto Rico, 00909
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?Ód?, Puola, 94-017
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Bytom, Puola, 41-902
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Poznan, Puola, 61-397
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Sosnowiec, Puola, 41-200
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Warsaw, Puola, 02-507
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Wroc?Aw, Puola, 50-368
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Bad Nauheim, Saksa, 61231
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Baden-Baden, Saksa, 76530
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Berlin, Saksa, 14059
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Erlangen, Saksa, 91054
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Freiburg, Saksa, 79106
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Hildesheim, Saksa, 31134
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Jena, Saksa, 07747
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Zerbst, Saksa, 39261
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Singapore, Singapore, 258499
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Bangkok, Thaimaa, 10700
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Chiang Mai, Thaimaa, 50200
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Donetsk, Ukraina, 83001
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Ivano-Frankivsk, Ukraina, 76008
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Kharkiv, Ukraina, 61029
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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
- 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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Odesa, Ukraina, 65025
- 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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Simferopol, Ukraina, 95017
- 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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Ternopil, Ukraina, 46002
- 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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Uzhorod, Ukraina, 88018
- 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.
-
Vinnytsya, Ukraina, 21018
- 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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Zaporizhzhia, Ukraina, 69600
- 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.
-
Zhytomyr, Ukraina, 10002
- 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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Brest, Valko-Venäjä, 224027
- 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.
-
Grodno, Valko-Venäjä, 230017
- 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.
-
Minsk, Valko-Venäjä, 220116
- 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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Alabama
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Birmingham, Alabama, Yhdysvallat, 35294
- 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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Arizona
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Glendale, Arizona, Yhdysvallat, 85304
- 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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Mesa, Arizona, Yhdysvallat, 85202
- 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.
-
Paradise Valley, Arizona, Yhdysvallat, 85253
- 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, Arizona, Yhdysvallat, 85381
- 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.
-
Phoenix, Arizona, Yhdysvallat, 85037
- 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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Arkansas
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Little Rock, Arkansas, Yhdysvallat, 72205
- 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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California
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Anaheim, California, Yhdysvallat, 92805
- 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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Glendale, California, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
Connecticut
-
Danbury, Connecticut, Yhdysvallat, 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.
-
Farmington, Connecticut, Yhdysvallat, 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.
-
Norwich, Connecticut, Yhdysvallat, 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.
-
Trumbull, Connecticut, Yhdysvallat, 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
-
Boca Raton, Florida, Yhdysvallat, 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.
-
Clearwater, Florida, Yhdysvallat, 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.
-
Doral, Florida, Yhdysvallat, 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.
-
Fort Lauderdale, Florida, Yhdysvallat, 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.
-
Jacksonville, Florida, Yhdysvallat, 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.
-
Lake Mary, Florida, Yhdysvallat, 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.
-
Miami, Florida, Yhdysvallat, 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.
-
Orange Park, Florida, Yhdysvallat, 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.
-
Palm Harbor, Florida, Yhdysvallat, 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.
-
Saint Petersburg, Florida, Yhdysvallat, 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.
-
Tamarac, Florida, Yhdysvallat, 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.
-
Tampa, Florida, Yhdysvallat, 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.
-
-
Georgia
-
Atlanta, Georgia, Yhdysvallat, 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.
-
Decatur, Georgia, Yhdysvallat, 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.
-
Marietta, Georgia, Yhdysvallat, 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.
-
-
Idaho
-
Boise, Idaho, Yhdysvallat, 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.
-
-
Illinois
-
Chicago, Illinois, Yhdysvallat, 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.
-
Peoria, Illinois, Yhdysvallat, 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.
-
-
Indiana
-
Muncie, Indiana, Yhdysvallat, 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.
-
-
Kansas
-
Kansas City, Kansas, Yhdysvallat, 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.
-
-
Kentucky
-
Bowling Green, Kentucky, Yhdysvallat, 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.
-
Lexington, Kentucky, Yhdysvallat, 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.
-
-
Maryland
-
Baltimore, Maryland, Yhdysvallat, 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.
-
Hagerstown, Maryland, Yhdysvallat, 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.
-
Wheaton, Maryland, Yhdysvallat, 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.
-
-
Michigan
-
Grand Rapids, Michigan, Yhdysvallat, 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.
-
-
Minnesota
-
Eagan, Minnesota, Yhdysvallat, 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.
-
-
Missouri
-
Florissant, Missouri, Yhdysvallat, 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.
-
-
Nebraska
-
Lincoln, Nebraska, Yhdysvallat, 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.
-
Omaha, Nebraska, Yhdysvallat, 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.
-
-
New Jersey
-
Clifton, New Jersey, Yhdysvallat, 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.
-
Teaneck, New Jersey, Yhdysvallat, 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.
-
Toms River, New Jersey, Yhdysvallat, 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.
-
-
New Mexico
-
Albuquerque, New Mexico, Yhdysvallat, 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.
-
-
New York
-
Bronx, New York, Yhdysvallat, 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.
-
Endwell, New York, Yhdysvallat, 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.
-
Manhasset, New York, Yhdysvallat, 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, Yhdysvallat, 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.
-
Rochester, New York, Yhdysvallat, 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
-
Charlotte, North Carolina, Yhdysvallat, 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.
-
Greenville, North Carolina, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
Ohio
-
Cincinnati, Ohio, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
Oklahoma
-
Edmond, Oklahoma, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Yhdysvallat, 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.
-
Pittsburgh, Pennsylvania, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
South Carolina
-
Columbia, South Carolina, Yhdysvallat, 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.
-
Greenville, South Carolina, Yhdysvallat, 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, Yhdysvallat, 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.
-
-
Tennessee
-
Crossville, Tennessee, Yhdysvallat, 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.
-
Hixon, Tennessee, Yhdysvallat, 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.
-
Jackson, Tennessee, Yhdysvallat, 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.
-
-
Texas
-
Allen, Texas, Yhdysvallat, 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.
-
Dallas, Texas, Yhdysvallat, 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.
-
Houston, Texas, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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.
-
Waco, Texas, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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.
-
Richmond, Virginia, Yhdysvallat, 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.
-
Williamsburg, Virginia, Yhdysvallat, 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, Yhdysvallat, 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, Yhdysvallat, 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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Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
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
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Nelinkertaistaa
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
---|---|
Placebo Comparator: Plasebo
Annettu SC
|
Muut nimet:
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
|
Kokeellinen: LY2127399 every 2 weeks
Administered SC
|
120 mg administered via subcutaneous (SC) injection for 52 weeks.
240 mg loading dose will be administered as the first dose of study drug.
Muut nimet:
|
Kokeellinen: LY2127399 every 4 wks
During the Treatment Period, for blinding purposes, patients will alternate injections of LY2127399 and injections of placebo every 2 weeks.
|
120 mg administered via subcutaneous (SC) injection for 52 weeks.
240 mg loading dose will be administered as the first dose of study drug.
Muut nimet:
Annettiin ihonalaisesti 52 viikon ajan.
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
---|---|---|
Niiden osallistujien prosenttiosuus, jotka saavuttivat SLE-vasteindeksin vastauksen viikolla 52
Aikaikkuna: 52 viikkoa
|
Niiden osallistujien prosenttiosuus, joiden SELENA SLEDAI -pistemäärä on laskenut ≥ 5 pistettä lähtötasosta, eikä PGA:ssa heikentynyt (lisäys < 0,30 pistettä lähtötasosta), eikä uusia BILAG A -elinaluepisteitä tai kahta uutta BILAG B -elinalueen pistettä verrattuna lähtötasoon . SELENA SLEDAI lasketaan 24 yksittäisestä kuvauksesta 9 elinjärjestelmässä; 0 tarkoittaa inaktiivista sairautta ja suurin teoreettinen pistemäärä on 105; pisteet > 20 ovat harvinaisia. PGA on visuaalinen analoginen asteikko 0-3 (0 = ei mitään, 1 = lievä, 2 = kohtalainen, 3 = vaikea). BILAG käyttää yhtä pistemäärää kullekin 9 elinalueelle; vaihteluväli on vakavasta (A) ei sairauteen (E). Osallistujat, jotka eivät kyenneet noudattamaan sallittuja samanaikaisten lääkkeiden vaatimuksia, katsottiin ei-vastettaviksi, samoin kuin osallistujat, jotka keskeyttivät tai puuttuivat viikon 52 tiedot. |
52 viikkoa
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
---|---|---|
Percentage Participants Able to Decrease Dose of Prednisone or Equivalent With No Increase in Disease Activity at Week 52
Aikaikkuna: 52 weeks
|
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.
|
52 weeks
|
Muutos lähtötilanteesta 52 viikkoon anti-kaksoisjuosteisen deoksiribonukleiinihapon (anti-dsDNA) tasolla
Aikaikkuna: Lähtötilanne, 52 viikkoa
|
Anti-kaksijuosteinen deoksiribonukleiinihappo (anti-dsDNA) on laboratorioanalyytti, jota käytetään auttamaan SLE:n diagnosoinnissa.
|
Lähtötilanne, 52 viikkoa
|
Muutos lähtötilanteesta 52 viikon päätepisteeseen systeemisen lupus erythematosus -taudin aktiivisuusindeksissä (SLEDAI2K)
Aikaikkuna: Lähtötilanne, 52 viikkoa
|
SLE-taudin aktiivisuusindeksin 2000 (SLEDAI-2K) pistemäärä on lupustaudin aktiivisuuden painotettu kumulatiivinen indeksi.
SLEDAI-2K lasketaan 24 yksittäisestä kuvauksesta 9 elinjärjestelmässä; 0 tarkoittaa inaktiivista sairautta ja teoreettinen enimmäispistemäärä on 105.
|
Lähtötilanne, 52 viikkoa
|
Aika ensimmäiseen vakavaan SLE-oireyhtymään (SFI)
Aikaikkuna: Lähtötilanne 52 viikon ajan
|
SFI käyttää SELENA-SLEDAI-taudin aktiivisuusindeksiä, taudin aktiivisuusskenaarioita, hoitomuutoksia ja PGA:ta määrittääkseen lieviä/kohtalaisia ja vakavia pahenemisvaiheita. Indeksi ottaa huomioon kokonaispisteiden absoluuttisen muutoksen, uudet tai pahenevat oireet sekä sairauden aktiivisuudesta johtuvan kortikosteroidien käytön tai sairaalahoidon lisääntymisen. Aika ensimmäiseen vakavaan SLE:n pahenemiseen (SFI) (päivinä) lasketaan seuraavasti: (Ensimmäisen vakavan SLE-leimauksen (SFI) alkamispäivä - satunnaistamisen päivämäärä + 1). |
Lähtötilanne 52 viikon ajan
|
Percentage of Participants With No Worsening in Physician Global Assessment (PGA) Score at 52 Weeks
Aikaikkuna: 52 weeks
|
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.
|
52 weeks
|
Muutos perustilanteesta 52 viikon päätepisteeseen lyhyen väsymyskartoituksen (BFI) pisteissä
Aikaikkuna: Lähtötilanne, 52 viikkoa
|
Osallistujien raportoima asteikko, joka mittaa väsymyksen vakavuutta viimeisen 24 tunnin aikana koetun pahimman väsymyksen perusteella.
Vakavuuspisteet vaihtelivat 0:sta (ei väsymystä) 10:een (niin vakava väsymys kuin voit kuvitella).
|
Lähtötilanne, 52 viikkoa
|
Change From Baseline to 52 Week Endpoint Lupus Quality of Life (LupusQoL) Domain Scores
Aikaikkuna: Baseline, 52 weeks
|
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.
|
Baseline, 52 weeks
|
Aika ensimmäiseen New British Isles Lupus Assessment Groupiin (BILAG A) tai 2 uuteen BILAG B SLE-soittimeen
Aikaikkuna: Lähtötilanne 52 viikon ajan
|
British Isles Lupus Assessment Group (BILAG) -instrumentti arvioi maailmanlaajuisen sairauden aktiivisuuden 9 elinjärjestelmän alueella. BILAG-leimaus arvioidaan kullekin yhdeksästä elinalueesta käyttämällä BILAG2004-indeksin flare-sääntöjä; A on voimakas leimahdus ja B on kohtalainen. Aika ensimmäiseen BILAG A:seen tai kahteen BILAG B-soihdutukseen (päivinä) lasketaan seuraavasti: (Ensimmäisen BILAG A:n tai kahden BILAG B:n alkamispäivämäärä - satunnaistamisen päivämäärä + 1). Kahden BILAG B -soihdun on tapahduttava eri aloilla samalla käynnillä. |
Lähtötilanne 52 viikon ajan
|
Change From Baseline to 52 Week Endpoint in PGA
Aikaikkuna: Baseline, 52 weeks
|
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.
|
Baseline, 52 weeks
|
Niiden osallistujien prosenttiosuus, joiden kortikosteroidiannos on kasvanut 52 viikon kohdalla
Aikaikkuna: 52 viikkoa
|
Kortikosteroidien nousu käynnin aikana määriteltiin muutokseksi lähtötasosta yli 2,5 mg/vrk annoksessa tai prednisonissa tai vastaavassa käyttämällä edellisen suunnitellusta käynnistä otetun kortikosteroidien keskimääräistä päivittäistä annosta.
|
52 viikkoa
|
Muutos lähtötilanteesta 52 viikon päätepisteeseen SELENA-SLEDAI-taudin aktiivisuuspisteissä
Aikaikkuna: Lähtötilanne, 52 viikkoa
|
Estrogeenien turvallisuus lupus erythematosus -tutkimuksessa National Assessment - SLE-taudin aktiivisuusindeksi (SELENA-SLEDAI) on painotettu, kumulatiivinen indeksi lupus-taudin aktiivisuudesta.
SELENA-SLEDAI lasketaan 24 yksittäisestä kuvauksesta 9 elinjärjestelmässä; 0 tarkoittaa inaktiivista sairautta ja teoreettinen enimmäispistemäärä on 105.
|
Lähtötilanne, 52 viikkoa
|
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
Aikaikkuna: 52 weeks
|
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
|
Number of Participants With No New BILAG A and No More Than One New BILAG B Disease Activity Scores Compared to Baseline
Aikaikkuna: Baseline through 52 weeks
|
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
|
Yhteistyökumppanit ja tutkijat
Sponsori
Julkaisuja ja hyödyllisiä linkkejä
Yleiset julkaisut
- 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.
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Arvio)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
- Immuunijärjestelmän sairaudet
- Lupus erythematosus, systeeminen
- Sidekudostaudit
- Autoimmuunisairaudet
- Huumeiden fysiologiset vaikutukset
- Infektiota estävät aineet
- Ääreishermoston aineet
- Analgeetit
- Aistijärjestelmän agentit
- Analgeetit, ei-huumeet
- Reumaattiset aineet
- Immunologiset tekijät
- Alkueläinten vastaiset aineet
- Antiparasiittiset aineet
- Tulehdusta ehkäisevät aineet
- Immunosuppressiiviset aineet
- Tulehduskipuaineet, ei-steroidiset
- Malarialääkkeet
Muut tutkimustunnusnumerot
- 13656
- H9B-MC -BCDS (Muu tunniste: Eli Lilly and Company)
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
Yhdysvalloissa valmistettu ja sieltä viety tuote
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .
Kliiniset tutkimukset Systeeminen lupus erythematosus
-
European Society for Blood and Marrow TransplantationEULARPeruutettuTulenkestävä SYSTEMIC LUPUS ERYTHEMATOSUSRanska
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BiogenRekrytointiSubakuutti ihon lupus erythematosus | Krooninen ihon lupus erythematosusYhdysvallat, Italia, Korean tasavalta, Taiwan, Argentiina, Chile, Espanja, Kanada, Serbia, Ranska, Saksa, Japani, Brasilia, Yhdistynyt kuningaskunta, Puerto Rico, Bulgaria, Portugali, Sveitsi, Filippiinit, Saudi-Arabia, Ruotsi, ... ja enemmän
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Florida Academic Dermatology CentersTuntematonDiscoid lupus erythematosus (DLE)Yhdysvallat
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BiogenIlmoittautuminen kutsustaSubakuutti ihon lupus erythematosus | Krooninen ihon lupus erythematosusRanska, Espanja, Yhdysvallat, Ruotsi
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AmgenValmis
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Bristol-Myers SquibbAktiivinen, ei rekrytointiLupus Erythematosus, Discoid | Lupus erythematosus, subakuutti ihoMeksiko, Argentiina, Australia, Yhdysvallat, Ranska, Saksa, Puola, Taiwan
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SanofiValmisIhon lupus erythematosus - systeeminen lupus erythematosusJapani
-
LEO PharmaLopetettuDiscoid lupus erythematosusYhdysvallat, Ranska, Saksa, Tanska
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University of PennsylvaniaRekrytointiIhon lupus erythematosus (CLE)Yhdysvallat
-
Novartis PharmaceuticalsValmisSubakuutti ihon lupus erythematosusKreikka, Saksa, Italia
Kliiniset tutkimukset LY2127399
-
Eli Lilly and CompanyLopetettuNivelreumaArgentiina, Saksa, Intia, Korean tasavalta, Yhdysvallat, Unkari, Taiwan, Bulgaria, Ranska, Venäjän federaatio, Espanja, Ukraina, Kolumbia, Meksiko, Puola, Japani, Kroatia, Kreikka, Uusi Seelanti, Romania, Etelä-Afrikka, Australia, Brasili... ja enemmän
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Eli Lilly and CompanyValmisMunuaisten vajaatoiminta, krooninenYhdysvallat
-
Applied Molecular EvolutionEli Lilly and CompanyValmisMultippeli myeloomaYhdysvallat
-
Eli Lilly and CompanyLopetettuNivelreumaYhdysvallat, Saksa, Taiwan, Ranska, Japani, Meksiko, Puola, Venäjän federaatio, Espanja, Kolumbia, Argentiina, Kreikka, Uusi Seelanti, Etelä-Afrikka, Australia, Korean tasavalta, Brasilia, Italia, Malesia
-
Eli Lilly and CompanyValmisNivelreumaArgentiina, Intia, Yhdysvallat, Unkari, Bulgaria, Meksiko, Ukraina, Kolumbia, Taiwan, Puola, Japani, Korean tasavalta, Uusi Seelanti, Romania, Etelä-Afrikka, Australia, Kroatia, Liettua, Malesia, Venäjän federaatio, Slovakia, Sri...
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Eli Lilly and CompanyLopetettuSysteeminen lupus erythematosus | Autoimmuuni sairaus | SidekudostautiYhdysvallat
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Eli Lilly and CompanyValmisSysteeminen lupus erythematosus | Autoimmuuni sairaus | SidekudostautiIntia, Yhdysvallat, Unkari, Romania, Espanja, Ranska, Taiwan, Venäjän federaatio, Yhdistynyt kuningaskunta, Australia, Latvia, Meksiko, Etelä-Afrikka, Kanada, Israel, Brasilia, Serbia, Ecuador, Malesia, Uusi Seelanti, Tunisia
-
Eli Lilly and CompanyValmis
-
Eli Lilly and CompanyValmisNivelreumaYhdysvallat, Meksiko, Unkari, Intia, Argentiina, Chile, Ukraina, Australia, Romania, Saksa, Puola, Slovakia