A Clinical Trial of BP1002 in Patients With Advanced Lymphoid Malignancies

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

November 5, 2020

Primary Completion Date

April 30, 2025

Study Completion Date

April 30, 2025

Conditions
Mantle Cell LymphomaPeripheral T-cell Lymphoma (PTCL)Cutaneous T-cell Lymphoma (CTCL)Chronic Lymphocytic Leukemia (CLL)Small Lymphocytic Lymphoma (SLL)Follicular LymphomaMarginal Zone LymphomaHodgkin LymphomaWaldenstrom MacroglobulinemiaDLBCL
Interventions
DRUG

L-Bcl-2 antisense oligonucleotide

There will be 2 planned dose levels, 20, and 40 mg/m\^2. Successive cohorts of eligible patients with will be treated with BP1002. BP1002 is given as an intravenous infusion, twice weekly, as 8 doses per 28-day cycle. Cycles may be repeated every 4 weeks.

Trial Locations (5)

10595

New York Medical College / Westchester Medical Center, Valhalla

30912

Georgia Cancer Center, Augusta

37203

Sarah Cannon Research Institute/Tennesee Oncology, Nashville

75390

University of Texas Southwestern Medical Center, Dallas

77030

MD Anderson Cancer Research Center, Houston

Sponsors
All Listed Sponsors
lead

Bio-Path Holdings, Inc.

INDUSTRY