Oral Rigosertib in Low Risk MDS Patients Refractory to ESAs

PHASE2CompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

July 31, 2013

Primary Completion Date

December 31, 2020

Study Completion Date

May 31, 2021

Conditions
Myelodysplastic Syndromes
Interventions
DRUG

Oral rigosertib

Dose of 560 mg consists of two (2) 280 mg soft gel capsules of rigosertib.

Trial Locations (14)

10029

Mount Sinai Medical Center, New York

20010

Washington Cancer Institute at Medstar Washington Hospital Center, Washington D.C.

21201

Greenbaum Cancer Center University of Maryland, Baltimore

40225

Heinrich Heine Universität, Düsseldorf

44195

Cleveland Clinic Foundation, Cleveland

50937

Universitätsklinikum Köln, Cologne

55905

Mayo Clinic, Rochester

60637

The University of Chicago, Chicago

75475

Hôpital Saint-Louis, Service d'Hématologie, Paris

77030

The University of Texas MD Anderson Cancer Center, Houston

80045

Anschutz Cancer Pavilion University of Colorado, Aurora

94305

Stanford University School of Medicine, Stanford

08903

Rutgers Cancer Institute of New Jersey, New Brunswick

01307

Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden

All Listed Sponsors
lead

Traws Pharma, Inc.

INDUSTRY

NCT01904682 - Oral Rigosertib in Low Risk MDS Patients Refractory to ESAs | Biotech Hunter | Biotech Hunter