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Trial Information

Randomized Placebo Controlled Trial of Budesonide MMX® 9 mg in Patients With Ulcerative Colitis Currently on a 5-ASA

Official Title:

Summary

This study is to compare the efficacy and safety of budesonide MMX 9 mg versus placebo as add-on therapy to an existing oral 5-ASA regimen for the induction of remission in patients with active, mild or moderate ulcerative colitis (UC).

Phase: Phase 3

Sponsor: Santarus

Overall Contacts:

Michael Huang, MD
858/314-5700

Karissa Tranel, PhD
Phone: 858/314-5772

Locations (129)

Country State City Zip Facility and Contact
United States California Anaheim 92801 Santarus Clinical Investigational Site 1043
United States California Lakewood 90712 Santarus Clinical Investigational Site 1071
United States California Los Angeles 90301 Santarus Clinical Investigational Site 1051
United States California San Diego 92114 Santarus Clinical Investigational Site 1003
United States California San Diego 92123 Santarus Clinical Investigational Site 1053
United States Colorado Littleton 80120 Santarus Clinical Investigational Site 1063
United States Connecticut Bristol 06010 Santarus Clinical Investigational Site 1028
United States Connecticut Hamden 06518 Santarus Clinical Investigational Site 1018
United States Florida Boynton 33426 Santarus Clinical Investigational Site 1035
United States Florida Jacksonville 32256 Santarus Clinical Investigational Site 1045
United States Florida Largo 33777 Santarus Clinical Investigational Site 1001
United States Florida Maitland 32751 Santarus Clinical Investigational Site 1024
United States Florida Miramar 33025 Santarus Clinical Investigational Site 1013
United States Florida Port Orange 32127 Santarus Clinical Investigational Site 1029
United States Florida Winter Park 32789 Santarus Clinical Investigational Site 1010
United States Florida Zephyrhills 33613 Santarus Clinical Investigational Site 1002
United States Georgia Decatur 30033 Santarus Clinical Investigational Site 1050
United States Georgia Marietta 30060 Santarus Clinical Investigational Site 1085
United States Illinois Chicago 60637 Santarus Clinical Investigational Site 1075
United States Illinois Oak Lawn 60453 Santarus Clinical Investigational Site 1065
United States Indiana Indianapolis 46202 Santarus Clinical Investigational Site 1058
United States Iowa Clive 50325 Santarus Clinical Investigational Site 1008
United States Louisiana Metairie 70006 Santarus Clinical Investigational Site 1034
United States Louisiana Shreveport 71103 Santarus Clinical Investigational Site 1032
United States Maryland Annapolis 21401 Santarus Clinical Investigational Site 1044
United States Maryland Chevy Chase 20815 Santarus Clinical Investigational Site 1057
United States Maryland Hollywood 20636 Santarus Clinical Investigational Site 1012
United States Michigan Chesterfield 48047 Santarus Clinical Investigational Site 1016
United States Michigan Novi 48377 Santarus Clinical Investigational Site 1081
United States Michigan Wyoming 49159 Santarus Clinical Investigational Site 1015
United States Michigan Ypsilanti 48197 Santarus Clinical Investigational Site 1068
United States Minnesota Rochester 55905 Santarus Clinical Investigational Site 1074
United States New Hampshire Lebanon 03756 Santarus Clinical Investigational Site 1061
United States New York Cheektowaga 14225 Santarus Clinical Investigational Site 1021
United States New York Great Neck 11023 Santarus Clinical Investigational Site 1072
United States New York Lake Success 11042 Santarus Clinical Investigational Site 1067
United States New York New York 10028 Santarus Clinical Investigational Site 1031
United States North Carolina Wilmington 28403 Santarus Clinical Investigational Site 1073
United States Ohio Cincinati 45267 Santarus Clinical Investigational Site 1080
United States Ohio Cleveland 44195 Santarus Clinical Investigational Site 1078
United States Ohio Dayton 45415 Santarus Clinical Investigational Site 1082
United States Pennsylvania Lancaster 17604 Santarus Clinical Investigational Site 1064
United States Pennsylvania Sayre 18840 Santarus Clinical Investigational Site 1006
United States Texas Austin 78705 Santarus Clinical Investigational Site 1059
United States Texas Houston 77090 Santarus Clinical Investigational Site 1019
United States Texas Houston 77030 Santarus Clinical Investigational Site 1004
United States Texas Houston 77030 Santarus Clinical Investigational Site 1039
United States Texas Pasadena 77505 Santarus Clinical Investigational Site 1005
United States Texas The Woodlands 77388 Santarus Clinical Investigational Site 1048
United States Utah Lancaster 84341 Santarus Clinical Investigational Site 1014
United States Utah Ogden 84405 Santarus Clinical Investigational Site 1020
United States Virginia Chesapeake 23320 Santarus Clinical Investigational Site 1038
United States Virginia Christianburg 24073 Santarus Clinical Investigational Site 1025
United States Wisconsin Madison 53715 Santarus Clinical Investigational Site 1036
Bulgaria Pleven Santarus Clinical Investigational Site 4003
Bulgaria Plovdiv Santarus Clinical Investigational Site 4009
Bulgaria Plovdiv Santarus Clinical Investigational Site 4004
Bulgaria Ruse Santarus Clinical Investigational Site 4008
Bulgaria Sofia Santarus Clinical Investigational Site 4001
Bulgaria Sofia Santarus Clinical Investigational Site 4002
Bulgaria Sofia Santarus Clinical Investigational Site 4005
Bulgaria Sofia Santarus Clinical Investigational Site 4010
Bulgaria Sofia Santarus Clinical Investigational Site 4007
Bulgaria Sofia Santarus Clinical Investigational Site 4011
Canada Manitoba Winnipeg R3A1R9 Santarus Clinical Investigational Site 2003
Canada Nova Scotia Halifax Santarus Clinical Investigational Site 2008
Canada Ontario London Santarus Clinical Investigational Site 2004
Canada Ontario Ottawa Santarus Clinical Investigational Site 2010
Canada Ontario Vaughan L4L4Y7 Santarus Clinical Investigational Site 2002
Canada Quebec Montreal Santarus Clinical Investigational Site 2009
Canada Quebec Sherbrooke J1G2E8 Santarus Clinical Investigational Site 2001
Canada Calgary Santarus Clinical Investigational Site 2007
Canada London Santarus Clinical Investigational Site 2005
Canada Quebec Santarus Clinical Investigational Site 2006
Czech Republic Hradec Kralove Santarus Clinical Investigational Site 3006
Czech Republic Hradec Kralove Santarus Clinical Investigational Site 3001
Czech Republic Labem Santarus Clinical Investigational Site 3005
Czech Republic Olomouc Santarus Clinical Investigational Site 3003
Czech Republic Prague Santarus Clinical Investigational Site 3009
Czech Republic Praha Santarus Clinical Investigational Site 3007
Czech Republic Praha Santarus Clinical Investigational Site 3004
Czech Republic Tabor Santarus Clinical Investigational Site 3002
Czech Republic Usti nad Orlici Santarus Clinical Investigational Site 3010
Czech Republic Valasske Mezirici Santarus Clinical Investigational Site 3011
Estonia Tallinn Santarus Clinical Investigational Site 8001
Hungary Bekescsaba Santarus Clinical Investigational Site 5010
Hungary Budapest Santarus Clinical Investigational Site 5008
Hungary Budapest Santarus Clinical Investigational Site 5009
Hungary Debrecen Santarus Clinical Investigational Site 5001
Hungary Gyula Santarus Clinical Investigational Site 5003
Hungary Kaposvar Santarus Clinical Investigational Site 5004
Hungary Miskolc Santarus Clinical Investigational Site 5002
Hungary Mosonmagyarovar Santarus Clinical Investigational Site 5006
Hungary Pecs Santarus Clinical Investigational Site 5011
Hungary Szeged Santarus Clinical Investigational Site 5005
Hungary Vac Santarus Clinical Investigational Site 5007
Latvia Riga Santarus Clinical Investigational Site 8103
Latvia Riga Santarus Clinical Investigational Site 8101
Latvia Riga Santarus Clinical Investigational Site 8102
Lithuania Kaunas Santarus Clinical Investigational Site 8202
Lithuania Vilnius Santarus Clinical Investigational Site 8201
Lithuania Vilnius Santarus Clinical Investigational Site 8203
Poland Elblag Santarus Clinical Investigational Site 6003
Poland Krakow Santarus Clinical Investigational Site 6001
Poland Sopot Santarus Clinical Investigational Site 6002
Poland Szczecin Santarus Clinical Investigational Site 6006
Poland Warszawa Santarus Clinical Investigational Site 6004
Poland Warszawa Santarus Clinical Investigational Site 6008
Poland Warszawy Santarus Clinical Investigational Site 6005
Russian Federation Lipetsk Santarus Clinical Investigational Site 9016
Russian Federation Moscow Santarus Clinical Investigational Site 9010
Russian Federation Moscow Santarus Clinical Investigational Site 9005
Russian Federation Nizhny Novgorod Santarus Clinical Investigational Site 9004
Russian Federation Ryazan Santarus Clinical Investigational Site 9003
Russian Federation Saint Petersburg Santarus Clinical Investigational Site 9014
Russian Federation Saint Petersburg Santarus Clinical Investigational Site 9008
Russian Federation Saint Petersburg Santarus Clinical Investigational Site 9013
Russian Federation Saratov Santarus Clinical Investigational Site 9009
Russian Federation St Petersburg Santarus Clinical Investigational Site 9001
Russian Federation Stavropol Santarus Clinical Investigational Site 9007
Russian Federation Ufa Santarus Clinical Investigational Site 9006
Russian Federation Volgograd Santarus Clinical Investigational Site 9017
Ukraine Crimea Santarus Clinical Investigational Site 7010
Ukraine Donetsk Santarus Clinical Investigational Site 7002
Ukraine Kharkiv Santarus Clinical Investigational Site 7004
Ukraine Kharkiv Santarus Clinical Investigational Site 7001
Ukraine Kyiv Santarus Clinical Investigational Site 7008
Ukraine Kyiv Santarus Clinical Investigational Site 7006
Ukraine Vinnytsia Santarus Clinical Investigational Site 7005

NCT ID:NCT01532648

Date Last Changed: April 10, 2013