A Clinical Trial of BP1002 in Patients With Advanced Lymphoid Malignancies

Running, not enrolling · Phase 1

Conditions studied: Mantle Cell Lymphoma, Peripheral T-cell Lymphoma (PTCL), Cutaneous T-cell Lymphoma (CTCL), Chronic Lymphocytic Leukemia (CLL), Small Lymphocytic Lymphoma (SLL), Follicular Lymphoma, Marginal Zone Lymphoma, Hodgkin Lymphoma, Waldenstrom Macroglobulinemia, DLBCL

In brief

This study evaluates the safety, pharmacokinetics, and efficacy of BP1002 (L-Bcl-2) antisense oligonucleotide in patients with advanced lymphoid malignancies. Up to 12 evaluable patients with a diagnosis of relapsed or refractory lymphoid malignancies are expected to participate.

Key facts

Study ID: NCT04072458
Run by: Bio-Path Holdings, Inc.
People needed: 30
Starts: 2020-11-05
Expected to finish: 2025-04-01
Last updated by the study team: 2025-02-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Adults ≥18 years of age
Patient has a life expectancy ≥ 3 month
Patient has relapsed or refractory disease Relapsed lymphoma: Relapsed lymphoma is disease that has responded to treatment but then returns.
Refractory lymphoma: Failure to achieve complete response at the end of therapy or progression within 6 months from completion of therapy
Included Diseases
DLBCL, including transformed lymphoma
Mantle Cell Lymphoma
PTCL
CTCL
CLL/SLL
Follicular lymphoma
Marginal zone lymphoma
Hodgkin lymphoma (both classical and lymphocyte predominant)
Waldenströms Macroglobulinemia
Must has failed or is not a candidate for available therapies with reasonable likelihood of clinical benefit, which includes FDA approved products and standard of care regimens
Therapy means at least three front lines of therapy including Hematopoeitic Stem Cell Transplant (HSCT and/or Chimeric Antigen Receptor (CAR) T cells, when applicable
Females must be of non-childbearing potential, surgically sterile, postmenopausal, or practice adequate methods of contraception during the study
Males must agree to use an adequate method of contraception during the study
Eastern Cooperative Oncology Group (ECOG) Performance score of 0, 1, or 2
Adequate hepatic and renal functions as defined by:
Aspartate transaminase (AST) and alanine transaminase (ALT) ≤2.5 times the upper limit of normal (ULN); and
Total bilirubin ≤1.5 times ULN; and
Estimated glomerular filtration rate (eGFR) of at least 50ml/min. These estimations can be calculated using the following methods:
Chronic Kidney Disease Epidemiology Collaboration (CKD-Epi) equation
Cockcroft Gault equation

You may not qualify if…

Active non-hematologic malignancy other than lymphoid malignancies treated with immuno- or chemotherapy within the previous 12 months except active non-melanoma, non-invasive skin cancer will be allowed
Known, active Central Nervous System (CNS) involvement of disease requiring intrathecal therapy. Note: Patients with a history of CNS disease may be allowed to participate based on at least 1 documented, negative spinal fluid assessment within 28 days prior to Screening
Patient eligible for high dose chemotherapy and autologous stem cell transplant
Indolent non-Hodgkin lymphoma (iNHL)
Patients at high risk of Tumor Lysis Syndrome (TLS)
a. Bulky disease i. A unidimensional lesion greater than 10 cm and/or b. Lymphocyte count greater than 25,000 per µL
Receipt of any anti-cancer therapy within 14 days prior to Cycle 1 Day 1 (C1D1)
Uncontrolled active, untreated, or progressive infection
Receipt of any investigational agent or on study treatment within 30 days prior to C1D1
Females who are pregnant, test positive for pregnancy, or are breast-feeding during the Screening period, or intend to become pregnant or breast-feed during the course of the study or within 30 days after last dose of study drug
Serious intercurrent medical or psychiatric illness which, in the opinion of the Investigator, would interfere with the ability of the participant to complete the study
Active hepatitis B infection (based on positive surface antigen [HBsAg]), hepatitis C infection (based on Hepatitis C Virus (HCV) positive antibody [HCV Ab]), or human immunodeficiency virus (HIV-1 or HIV-2, based on positive antibody)
Presence of concurrent conditions that, in the opinion of the Investigator and/or Medical Monitor, may compromise or interfere with any aspect of study conduct or interpretation of results. This includes, but is not limited to, unstable or uncontrolled angina, New York Heart Association (NYHA) class III or IV congestive heart failure, uncontrolled and sustained hypertension, clinically significant cardiac dysrhythmia or clinically significant baseline EKG abnormality (e.g., QTcF >470 msec)
Within the past 6 months, has had any of the following: myocardial infarction, unstable angina pectoris, coronary/peripheral artery bypass graft, cerebrovascular accident or transient ischemic attack
Uncontrolled seizure disorder
Unable or unwilling to communicate or cooperate with the Investigator or follow the protocol for any reason.

Where it is running

Georgia Cancer Center — Augusta, Georgia, United States
New York Medical College / Westchester Medical Center — Valhalla, New York, United States
Sarah Cannon Research Institute/Tennesee Oncology — Nashville, Tennessee, United States
University of Texas Southwestern Medical Center — Dallas, Texas, United States
MD Anderson Cancer Research Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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