8
Participants
Start Date
September 30, 2014
Primary Completion Date
January 31, 2018
Study Completion Date
July 31, 2018
Sodium cridanimod
Eligible patients will be enrolled into the study and administered sodium cridanimod (500 mg i.m./ twice a week) in combination with megestrol acetate (160 mg p.o./ day) or medroxyprogesterone acetate (200 mg p.o./ day).
Montefiore Medical Center, The Bronx
Barbara Ann Karmanos Cancer Institute, Detroit
Physicians Research Group, San Jose
St. Jude Hospital Yorba Linda, St. Joseph's Heritage Healthcare, Santa Rosa
Brest Regional Clinical Hospital, Brest
Minsk City Clinical Oncology Dispensary, Minsk
N.N. Alexandrov National Cancer Centre of Belarus, Minsk
Vitebsk Regional Clinical Oncology Dispensary, Vitebsk
Masaryk Memorial Cancer Institute, Brno
University Hospital Hradec Kralove, Hradec Králové
University Hospital Olomouc, Oncology, Olomouc
Oncology Institute of Saint Alzbeta, Bratislava
Poko Poprad, s.r.o., Poprad
University Hospital Trencin, Trenčín
Cherkasy Regional Oncology Dispensary, Cherkasy
Municipal Institution of Dnipropetrovsk Regional Rada, Dnipropetrovsk
Kharkiv Regional Clinical Oncology Center, Kharkiv
S.P. Grigoryeva Institute of Medical Radiology, Kharkiv
Kherson Regional Oncological Dispensary, Kherson
Sumy State University, Sumy
Vinnitsa Regional Clinical Oncology Center, Vinnitsa
Collaborators (1)
Pharmasyntez
INDUSTRY
Kevelt AS
INDUSTRY