A Clinical Trial of BP1002 in Patients With Refractory/Relapsed Acute Myeloid Leukemia (AML)

• ClinicalTrials.gov Identifier: NCT05190471
• Recruitment Status: Recruiting
• First Posted: January 13, 2022
• Last Update Posted: December 20, 2022
• Sponsor: Bio-Path Holdings, Inc.
• Information provided by (Responsible Party): Bio-Path Holdings, Inc.

Study Description

Brief Summary:

This study evaluates the safety and tolerability of escalating doses of BP1002 (Liposomal Bcl-2 Antisense Oligodeoxynucleotide) in patients with refractory/relapsed AML. The study is designed to assess the safety profile, identify DLTs, biologically effective doses, PK, PD and potential anti-leukemic effects of BP1002 as single agent (dose escalation phase) followed by assessing BP1002 in combination with decitabine (dose expansion phase).

Condition or disease	Intervention/treatment	Phase
Acute Myeloid Leukemia, in Relapse; Acute Myeloid Leukemia Refractory	Drug: BP1002; Liposomal Bcl-2 Antisense Oligodeoxynucleotide; Drug: Decitabine (in combination with BP1002)	Phase 1

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 48 participants
• Allocation: Non-Randomized
• Intervention Model: Sequential Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase I/Ib Study of BP1002 (a Liposomal Bcl-2 Antisense Oligodeoxynucleotide) in Patients With Refractory/Relapsed Acute Myeloid Leukemia (AML)
• Actual Study Start Date: August 16, 2022
• Estimated Primary Completion Date: March 2024
• Estimated Study Completion Date: September 2024

Arms and Interventions

Arm	Intervention/treatment
Experimental: Relapsed/Refractory AML - BP1002 monotherapy; BP1002 monotherapy dose escalation	Drug: BP1002; Liposomal Bcl-2 Antisense Oligodeoxynucleotide; Dose escalation of BP1002 monotherapy; Other Name: Liposomal Bcl-2; L-Bcl-2
Experimental: Relapsed/Refractory AML - BP1002 in combination with decitabine; BP1002 single dose in combination with decitabine	Drug: BP1002; Liposomal Bcl-2 Antisense Oligodeoxynucleotide; Dose escalation of BP1002 monotherapy; Other Name: Liposomal Bcl-2; L-Bcl-2; Drug: Decitabine (in combination with BP1002); Dose expansion of BP1002 in combination with decitabine; Other Name: Decitabine

Outcome Measures

Primary Outcome Measures :

1. Identify Dose Limiting Toxicity (DLT) of BP1002 [ Time Frame: 30 days ]
   Identify DLT of BP1002 using non-hematologic and hematologic measures per NCI CTCAE criteria
2. Identify and grade treatment-emergent adverse events (TEAE) of escalating doses of BP1002 [ Time Frame: 30 days ]
   Identify TEAE of BP1002 using non-hematologic and hematologic measures per NCI CTCAE criteria
3. Identify and grade treatment-emergent laboratory abnormalities of escalating doses of BP1002 [ Time Frame: 30 days ]
   Identify and grade treatment-emergent laboratory abnormalities of escalating doses of BP1002 using non-hematologic and hematologic measure per NCI CTCAE criteria
4. Recommended Phase 2 (RP2D) of BP1002 [ Time Frame: 210 days ]
   Determine RP2D by evaluating Maximally Tolerated Dose (MTD) data
5. Determine plasma pharmacokinetics (PK) of BP1002 using maximum plasma drug concentration [ Time Frame: 30 days ]
   Evaluate plasma PK of BP1002 using maximum plasma drug concentration (Cmax)
6. Determine plasma pharmacokinetics (PK) of BP1002 using volume of distribution [ Time Frame: 30 days ]
   Evaluate in vivo PK of BP1002 using volume of distribution (Vd)
7. Determine plasma pharmacokinetics (PK) of BP1002 using elimination rate constant [ Time Frame: 30 days ]
   Evaluate in vivo PK of BP1002 using elimination rate constant
8. Determine half-life plasma pharmacokinetics (PK) of BP1002 [ Time Frame: 30 days ]
   Evaluate in vivo PK of BP1002 half-life (t1/2)
9. Identify conduction and rhythm changes (treatment emergent QTc elevations or other treatment emergent changes in ECG intervals) of escalating doses of BP1002 [ Time Frame: 30 days ]
   Collection of 12-lead ECGs at defined intervals to identify conduction and rhythm changes (treatment emergent QTc elevations or other treatment emergent changes in ECG intervals)
10. Determine pharmacodynamics (PD) of BP1002 [ Time Frame: 30 days ]
    Flow cytometry will be performed using peripheral blood to evaluate Bcl-2 target inhibition by BP1002 on pre and post treatment samples
11. Determine anti-drug antibody (ADA) levels of BP1002 [ Time Frame: 30 days ]
    Evaluate ADA via peripheral blood

Secondary Outcome Measures :

1. Determine evidence of response by bone marrow aspirate [ Time Frame: 180 days ]
   Assess complete remission (CR), CR with incomplete hematologic recovery (CRi), and CR with partial hematologic recovery (CRh) per Döhner 2017
2. Determine evidence of response by complete blood counts using peripheral blood [ Time Frame: 180 days ]
   Assess complete remission (CR), CR with incomplete hematologic recovery (CRi), and CR with partial hematologic recovery (CRh) per Döhner 2017
3. Assessment of morphologic leukemia free state (MLFS) and partial remissions by bone marrow aspirate and complete blood counts [ Time Frame: 180 days ]
   To assess percentage of participants with MLFS and partial remissions per Döhner 2017
4. Assessment of morphologic leukemia free state (MLFS) and partial remissions by bone marrow aspirate [ Time Frame: 180 days ]
   To assess percentage of participants with MLFS and partial remissions per Döhner 2017
5. Assessment of blast count reductions by complete blood counts using peripheral blood [ Time Frame: 180 days ]
   To assess blast count reductions per Williams 2016
6. To determine progression-free survival (PFS), overall survival (OS), and duration of response [ Time Frame: 180 days ]
   To assess progression-free survival (PFS), overall survival (OS), and duration of response from date of study entry to study closure or death

Other Outcome Measures:

1. Exploratory objective to correlate treatment response with cytogenetic characteristics [ Time Frame: 30 days ]
   Flow cytometry assays to determine the effects of BP1002 on Bcl-2 protein expression
2. Exploratory objective to correlate treatment response with molecular characteristics [ Time Frame: 30 days ]
   Flow cytometry assays to determine the effects of BP1002 on Bcl-2 protein expression

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

1. Adults ≥18 years of age, with histologic evidence of refractory/relapsed AML who have failed treatment with available therapies known to be active for refractory/relapsed AML
2. Eastern Cooperative Oncology Group (ECOG) Performance Status Score of 0, 1 or 2
3. For the dose expansion phase, participants with documented diagnosis of AML who are eligible for decitabine therapy

4. Participants must have adequate hepatic and renal functions as defined by:

   1. Aspartate transaminase (AST) and alanine transaminase (ALT) ≤2.5 times the upper limit of normal (ULN); and
   2. Usually total bilirubin ≤ 1.5 ULN. In specific cases the PI may request a waiver of this requirement with medical justification and agreement with the medical monitor and Bio-Path Holdings. And;
   3. Estimated creatinine clearance of at least 60 mL/min. These estimations are calculated using the Cockcroft-Gault equation.
5. Female participants of childbearing potential must agree to use an acceptable method of birth control (i.e. a hormonal contraceptive, intrauterine device, diaphragm with spermicide, condom with spermicide or abstinence) for the duration of the study and for at least 6 months after the last dose of study drug or decitabine
6. Male participants must agree to use an acceptable method of contraception for the duration of the study
7. Recovered from the effects of any prior surgery, radiotherapy, or antineoplastic treatment (with the exception of alopecia), based on Investigator assessment
8. Participants must be willing and able to provide written informed consent

Exclusion Criteria:

1. Active non-hematologic or lymphoid malignancy other than AML treated with immunotherapy, targeted therapy or chemotherapy within the previous 12 months
2. Known, active leptomeningeal leukemia requiring intrathecal therapy. NOTE: Participants 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
3. Isolated potentially treatable extramedullary leukemia without also meeting bone marrow criteria for acute leukemia (for AML usually ≥ 5% blasts in BMA or biopsy). Participants may have leukemia with lower blast counts (Döhner 2017). Bio-Path Holdings and Investigator concurrence required.
4. Acute promyelocytic leukemia (APL) with t(15;17)(q22;q12) PML-RARA
5. Chronic myeloid leukemia in any phase
6. Receipt of any anti-cancer therapy within 14 days prior to C1D1, with the exception of hydroxyurea or leukapheresis
7. Participants may not be receiving any other investigational agents
8. Female participants who are pregnant or breast-feeding
9. Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
10. Participants with human immunodeficiency virus (HIV) infection who have CD4+ T-cell counts < 350 cells/mcL or with clinically active hepatitis B or C infection
11. History of any hypersensitivity to hypomethylating agents, unless reaction is deemed irrelevant to the study by the Investigator and Medical Monitor
12. Unresolved toxicity higher than CTCAE Grade 1 attributed to any prior therapy or procedure, excluding alopecia
13. Presence of concurrent conditions that, in the opinion of the Investigator and/or Medical Monitor, may compromise the participant's ability to tolerate study treatment 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 ECG abnormality (e.g., QTcF >470 msec)
14. 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
15. Uncontrolled seizure disorder (i.e., seizures within the past 2 months)
16. Unable or unwilling to communicate or cooperate with the Investigator or follow the protocol for any reason

Contacts and Locations

Contacts

Contact: Michael Hickey; 832-742-1361; mhickey@biopathholdings.com

Locations

United States, California

UCLA Medical Center; Recruiting

Los Angeles, California, United States, 90024

Contact: Gary Schiller, MD

Principal Investigator: Gary Schiller, MD

United States, New York

Weill Cornell Medical College - NewYork-Presbyterian Hospital; Recruiting

New York, New York, United States, 10021

Contact: Dunay Bach 212-746-4447 dub4001@med.cornell.edu

Contact: Gail Roboz, MD 646-962-2700 gar2001@med.cornell.edu

Principal Investigator: Gail J Roboz, MD

United States, Texas

MD Anderson Cancer Center; Recruiting

Houston, Texas, United States, 77030

Contact: Miranda Lim, BSN, RN 713-794-1722 MGLim@mdanderson.org

Contact: Maro Ohanian, D.O. 713-792-2631 mohanian@mdanderson.org

Principal Investigator: Maro Ohanian, D.O.

Sponsors and Collaborators

Bio-Path Holdings, Inc.

Investigators

• Principal Investigator: Gail J Roboz, MD; Weill Cornell Medical College - New York-Presbyterian Hospital

More Information

• Responsible Party: Bio-Path Holdings, Inc.
• ClinicalTrials.gov Identifier: NCT05190471
• Other Study ID Numbers: BP1002-102-AML
• First Posted: January 13, 2022
• Last Update Posted: December 20, 2022
• Last Verified: October 2022

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:

Leukemia; Leukemia, Myeloid; Leukemia, Myeloid, Acute; Neoplasms by Histologic Type; Neoplasms; Decitabine; Oblimersen; Antimetabolites, Antineoplastic; Antimetabolites; Molecular Mechanisms of Pharmacological Action; Antineoplastic Agents; Enzyme Inhibitors