A Phase I/II Study of OPN-305 in Second-line Lower Risk Myelodysplastic Syndrome

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

96

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

December 31, 2018

Study Completion Date

December 31, 2018

Conditions
Myelodysplastic Syndrome
Interventions
DRUG

OPN-305

For the dose confirming part of the study, patients will receive a starting dose of 5 mg/kg OPN-305.

Trial Locations (4)

10021

Research Site, New York

10467

Research Site, The Bronx

33613

Research Site, Tampa

77030

Research Site, Houston

Sponsors
All Listed Sponsors
collaborator

M.D. Anderson Cancer Center

OTHER

collaborator

Montefiore Medical Center

OTHER

collaborator

H. Lee Moffitt Cancer Center and Research Institute

OTHER

collaborator

New York Presbyterian Hospital

OTHER

lead

Opsona Therapeutics Ltd.

INDUSTRY