Overview
The primary objectives of this study are to assess: (1) whether the combination of BP1001 plus venetoclax plus decitabine provides greater efficacy (Complete Remission [CR], Complete Remission with incomplete hematologic recovery [CRi], Complete Remission with partial hematologic recovery [CRh], than venetoclax plus decitabine alone (by historical comparison) in participants with untreated AML that cannot or elect not to be treated with more intensive chemotherapy; (2) whether BP1001-based treatment provides greater efficacy (CR, CRi, CRh) than intensive chemotherapy (by historical comparison) in participants with refractory/relapsed AML.
Description
Improvement of clinical benefit in fragile AML patients while maintaining tolerability is an important area of further clinical development. Modern aggressive combination chemotherapy can induce CR in a significant proportion of patients with previously untreated AML, but relapse occurs in most unless patients undergo intensive allogeneic hematopoietic stem cell transplantation. Novel therapies are needed for these patients
The Grb2 gene has been mapped to the human chromosome region 17q22-qter, a region that is duplicated in leukemias and solid tumors, which may result in an increased copy number of the Grb2 gene product. As Grb2 is important for the transformation of murine hematopoietic cells, and the proliferation of human leukemia cells that express high levels of oncogenic tyrosine kinases, inhibition of Grb2 may have a significant impact on the natural history of leukemias. The study drug (BP1001) may be able to inhibit the cells from making Grb-2. Researchers hope that without this protein, the leukemia cells will die.
This represents an area in which targeted therapies might be of benefit to these patients. One such potential treatment is BP1001, liposomal anti-sense treatment directed against Growth Factor Receptor-Bound Protein 2 (Grb2). Decitabine is approved in Europe for the treatment of adult patients with newly diagnosed de novo or secondary acute myeloid leukemia (AML). In vitro studies in AML cells co-incubated with BP1001 and decitabine suggests that treatment of AML patients with decitabine followed by BP1001 may be a combination that could benefit patients with AML.
This Phase IIa, multicenter, study of BP1001 in combination with Ventoclax plus decitabine will enroll participants with AML who are not otherwise eligible for for intensive induction therapy.
This trial will utilize an open label design to assess the safety profile, PK, PD, and efficacy of of BP1001 in combination with Ventoclax plus decitabine to assess whether the combination of either provides greater efficacy than intensive chemotherapy alone.
There are 3 cohorts exploring three-drug combinations of BP1001, venetoclax and decitabine.
- Untreated AML patients will be treated with BP1001 plus venetoclax plus decitabine.
- Refractory/relapsed AML patients will also be treated with BP1001 plus venetoclax plus decitabine.
- A third cohort of BP1001 + decitabine is offered to refractory/relapsed AML patients who are venetoclax resistant or intolerant, or not considered by the investigator as optimal candidates for venetoclax-based therapy.
Each cohort will continue until approximately 19 evaluable participants have been investigated. At that point, enrollment will be placed on hold so that the Sponsor can perform an administrative review of the data to determine which treatment cohorts should continue with enrollment.
Should one or more cohorts continue with enrollment, the sample size will be increased up to 54 in the refractory/relapsed AML cohorts and 98 in the untreated AML cohort. These sample sizes for the study are based on the primary endpoint.
Eligibility
Inclusion Criteria
At the time of Screening, participants must meet all of the following criteria to be
considered eligible to participate in the study:
1. Adults ≥18 years of age
2. Females must be of non-childbearing potential, surgically sterile, postmenopausal, or
practice adequate methods of contraception during the study and for 30 days after the
last dose of study drug or decitabine
3. Males must agree to use an adequate method of contraception during the study and for
at least 30 days after the last dose of study drug or decitabine
4. Histologically documented diagnosis (based on the 2008 World Health Organization [WHO]
Classification) (Vardiman et al. 2009) of one of the following:
1. Newly diagnosed untreated AML; or
2. Untreated secondary AML, including AML that has progressed from MDS
3. In some cases of AML associated with specific genetic abnormalities, however, the
diagnosis of AML may be made if the blast count is less than 20% (Dohner et al.
2017) - specifically AML with t(15;17), t(8;21), inv(16), or t(16;16))
4. Relapsed or Refractory AML
5. Investigator considers previously untreated participant ineligible for (or unwilling
to receive) intensive induction therapy based on medical reasons, disease
characteristics such as genetics, type of AML (untreated or secondary), or participant
characteristics such as age, performance status, co-morbidities, organ dysfunctions,
or patient election of low-intensity treatment
6. Eligible for venetoclax and decitabine therapy, based on Investigator assessment
7. Participant's WBC count is 25 x 10^9/L or less at study initiation. The use of
leukapheresis or hydroxyurea before treatment initiation to achieve this is permitted.
8. 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 glomerular filtration rate (eGFR) of at least 40 ml/min. These
estimations can be calculated using any of the following methods (Appendix E:
Formulas):
i. Chronic Kidney Disease Epidemiology Collaboration (CKD-Epi) equation
- GFR = 141 × min (Scr /κ, 1)^α × max(Scr /κ, 1)^-1.209 × 0.993^Age × 1.018 [if
female] × 1.159 [if black] ii. Cockcroft gault equation
- Cockcroft Gault equation utilizing the TBW (Total body weight) to calculate an
estimated creatinine clearance
- CrCl = [(140 - age) x TBW] / (Scr x 72) x 0.85 [if female] iii. Modification of
Diet in Renal Disease (MDRD) Study equation
- GFR (mL/min/1.73 m^2) = 175 × (Scr)^-1.154 × (Age)^-0.203 × 0.74 [if female] x
1.212 [if African American (AA)] iv. Creatinine clearance estimated by 24-hr
urine collection for creatinine clearance
9. Documented Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
10. Recovered from the effects of any prior surgery, radiotherapy, or antineoplastic
treatment (with the exception of alopecia), based on Investigator assessment
11. Willing and able to provide written informed consent 7.2. Exclusion Criteria
At the time of Screening, participants who meet any of the following criteria will be
excluded from participating in the study:
1. Active non-hematologic or lymphoid malignancy other than AML treated with immuno- or
chemotherapy within the previous 12 months except active non- melanoma, non-invasive
skin cancer will be allowed.
2. Known, active leptomeningeal leukemia 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
3. Isolated extramedullary leukemia without also meeting bone marrow criteria for acute
leukemia (for AML usually = 20% blasts in BMA or BMB). Patients may have leukemia with
lower blast counts (Dohner et al. 2010). Bio-Path Holdings and Investigator
concurrence required.
4. Acute promyelocytic leukemia (APL) with t(15;17)(q22;q12) PML-RARA
5. Chronic myeloid leukemia (CML) in any phase
6. Receipt of any anti-cancer therapy within 14 days prior to C1D1, with the exception of
hydroxyurea or anagrelide (within 24 hours), TKI (within 1day), a single dose of
cytarabine (for proliferative disease)
7. Uncontrolled active, untreated, or progressive infection
8. Receipt of any investigational agent or study treatment within 30 days prior to C1D1
9. Females who are capable of becoming 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
10. 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
11. Known active or clinically significant hepatitis B infection (based on positive
surface antigen [HBsAg]), hepatitis C infection (based on positive antibody [HCV Ab]),
or human immunodeficiency virus (HIV-1 or HIV-2, based on positive antibody)
12. History of any hypersensitivity to venetoclax or decitabine, unless reaction is deemed
irrelevant to the study by the Investigator and Medical Monitor
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. Cannot receive live attenuated vaccine immunization prior to, during, or after
treatment with venetoclax until B-cell recovery occurs
17. Unable or unwilling to communicate or cooperate with the Investigator or follow the
protocol for any reason