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Brief Title: A Phase 2 Study Comparing Chemotherapy in Combination With OGX-427 or Placebo in Patients With Bladder Cancer
Official Title: A Randomized, Double-blind Phase 2 Study Comparing Gemcitabine and Cisplatin in Combination With OGX-427 or Placebo in Patients With Advanced Transitional Cell Carcinoma
Study ID: NCT01454089
Brief Summary: The primary objective of this study is to ascertain whether there is evidence of longer survival relative to the control arm for three comparisons: 600 mg OGX-427 Arm to control Arm; 1000 mg OGX-427 Arm to control Arm; and pooled 600 mg and 1000 mg OGX-427 Arms to control Arm.
Detailed Description: Following 3 loading doses, participants receive chemotherapy and study drug on a 21-day cycle during the Treatment Period (Chemotherapy Period) until disease progression, completion of 6 cycles, toxicity or voluntary participant withdrawal. Participants who do not have documented disease progression and have completed a minimum of four cycles of chemotherapy continue to receive weekly Study Drug maintenance therapy during the Maintenance Period until disease progression or the participant fulfills one of the other reasons for withdrawal from protocol treatment, unless they have been discontinued from protocol treatment for unacceptable toxicity related to study drug. All participants have an End of Treatment (EOT) visit when they are withdrawn from all study treatment (chemotherapy and maintenance). All participants are followed until documented disease progression. Once disease progression is documented, participants enter a Survival Follow-up Period during which data are collected regarding further cancer therapy, secondary malignancy, and survival status.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
City of Hope National Medical Center, Duarte, California, United States
Cedars-Sinai Medical Center, Los Angeles, California, United States
University of California Los Angeles, Los Angeles, California, United States
USC Norris Comprehensive Cancer Center, Los Angeles, California, United States
Radiological Associates of Sacramento, Sacramento, California, United States
Yale University, New Haven, Connecticut, United States
Karmanos Cancer Institute, Detroit, Michigan, United States
Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, United States
Urology Cancer Center and GU Research Network, Omaha, Nebraska, United States
Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York, United States
Monter Cancer Center, Lake Success, New York, United States
Columbia University Medical Center, New York, New York, United States
Texas Oncology, P.A., Dallas, Texas, United States
Seattle Cancer Care Alliance, Seattle, Washington, United States
Tom Baker Cancer Center, Calgary, Alberta, Canada
Cross Cancer Center, Edmonton, Alberta, Canada
British Columbia Cancer Agency, Vancouver, British Columbia, Canada
Juravinski Cancer Centre, Hamilton, Ontario, Canada
R. S. McLaughlin Durham Regional Cancer Center at Lakeridge Health, Oshawa, Ontario, Canada
Princess Margaret Hospital, Toronto, Ontario, Canada
CHUM-Hospital Notre Dame, Montreal, Quebec, Canada
Centre Hospitalier Régional et Universitaire - Hôpital, Bretonneau Tours, Centre, France
Institute Jean Godinot, Reims, Champagne-Ardenne, France
Centre Hospitalier Universitaire de Rouen, Rouen, Haute-Normandie, France
Centre Hospitalier Universitaire, Institut Gustave Roussy, Villejuif Cedex, Ile-de-france, France
Centre Paul Papin, Angers Cedex 9, Pays De La Loire, France
Medicale Centre René Gauducheau, St. Herblain Cedex, Pays de la Loire, France
Institut Paoli Calmettes, Marseille Cedex 9, Provence Alpes Cote D'Azur, France
Centre Antoine Lacassagne, Nice, Provence Alpes Cote d'Azur, France
Universitätsklinikum Heidelberg, Heidelberg, Baden-Wuerttemberg, Germany
Klinikum Rechts der Isar der Technischen Universität, München, Bayern, Germany
Johann-Wolfgang-Goethe-Universität Frankfurt, Frankfurt, Hessen, Germany
Medizinische Hochschule Hannover, Hannover, Niedeersachen, Germany
Universitätsklinikum des Saarlandes, Homburg, Saarland, Germany
Universitätsklinikum Magdeburg A.ö.R., Magdeburg, Sachsen-Anhalt, Germany
Universitätsklinikum Dresden, Dresden, Sachsen, Germany
Universitätsklinikum Jena, Jena, Thuringen, Germany
Universitätsklinikum Mainz, Mainz, , Germany
Azienda Ospedaliero-Universitaria Policlinico di Modena, Modena, , Italy
Fondazione IRCCS Policlinico San Matteo Pavia, Pavia, , Italy
Unità Operativa di Oncologia Medica, Roma, , Italy
Akademicki Szpital Kliniczny im. J. Mikulicza-Radeckiego we Wroclawiu, Wroclaw, Dolnoslaskie, Poland
Centrum Onkologii im. Prof. Franciszka Lukaszczyka w Bydgoszczy, Bydgoszcz, Kujawsko-Pomorskie, Poland
NZOZ Europejskie Centrum Zdrowia Otwock, Otwock, Mazowieckie, Poland
Centrum Onkologii Instytut im. M. Sklodowskiej-Curie, Warszawa, Mazowieckie, Poland
Uniwersyteckie Centrum Kliniczne, Gdansk, Pomorskie, Poland
Zaklad Opieki Zdrowotnej MSWiA z Warminsko-Mazurskim Centrum Onkologii w Olsztynie, Olsztyn, Warminski-Mazurskie, Poland
Hospital Clinic I Provincial de Barcelona, Barcelona, , Spain
Hospital del Mar, Barcelona, , Spain
Hospital Santa Creu i Sant Pau, Barcelona, , Spain
Hospital Vall d´Hebrón, Barcelona, , Spain
Hospital General Universitario Gregorio Marañon, Madrid, , Spain
Hospital Universitario 12 de Octubre, Madrid, , Spain
Institut Català D'Oncologia, Hospital Duran i Reynals, Madrid, , Spain
Instituto Valenciano de Oncología-Fundación (IVO-FINCIVO), Valencia, , Spain
Name: Daniel Petrylak, MD
Affiliation: Columbia University
Role: PRINCIPAL_INVESTIGATOR