Study of Venetoclax in Combination With Decitabine in Subjects With Acute Myeloid Leukemia

Acute Myeloid Leukemia Clinical Trial

Official title:

Phase 1 Study of Venetoclax in Combination With Decitabine 10-Day Regimen in Subjects With Acute Myeloid Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03844815
• Other study ID #: IRB18-1498
• Status: Recruiting
• Phase: Phase 1
• Start date: November 18, 2019
• Est. completion date: June 10, 2025

Study information

• Verified date: August 2023
• Source: University of Chicago
• Contact: Cancer Clinical Trials Office
• Phone: 1-855-702-8222
• Email: cancerclinicaltrials[@]bsd.uchicago.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main purpose of this study is to learn about the safety and tolerability of an experimental drug, Venetoclax, when it is given along with Decitabine in subjects diagnosed with acute myeloid leukemia (AML).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 26
• Est. completion date: June 10, 2025
• Est. primary completion date: June 10, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Phase 1: Dose Escalation Phase

1. High risk AML, including any of the following:

1. Relapsed or refractory disease

2. TP53 mutant AML

3. Adverse risk cytogenetics including any of the following: 3 or more abnormalities; deletions involving chromosomes 5, 7, or 17; abnormalities in chromosome 11 involving MLL; t(6;9); inv(3) or t(3;3)

2. ECOG performance status 0-2

3. Age 18 years or older

4. Adequate organ function as defined by all of the following:

1. Creatinine clearance =30 mL/min, determined by the Cockroft-Gault formula, or measured by a 24 hour urine collection

2. AST and ALT =3 x ULN and bilirubin =1.5 x ULN (unless considered due to Gilbert's syndrome or of non-hepatic origin i.e. leukemic involvement).

5. Patients must be at least 2 weeks from major surgery, radiation therapy, or participation in other investigational trials, and must have recovered from clinically significant toxicities related to these prior treatments.

6. Patients must voluntarily sign and date an informed consent, approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), prior to the i initiation of any screening or study specific procedures.

7. Female patients of childbearing potential must have negative results for a pregnancy test

8. Patients must be willing to use appropriate contraception

• Phase 2: Dose Expansion Phase During the Phase 2 portion of the study, the subject population will be limited to patients with previously untreated AML with a mutation in TP53. All other inclusion criteria described above will apply.

Exclusion Criteria:

• Key exclusion criteria (apply to both Phase 1 and Phase 2 portions of the study):

1. Concomitant chemotherapy, radiation therapy, or immunotherapy other than as specified in this protocol

2. Patients suitable for and willing to receive intensive induction chemotherapy

3. Use of investigational agents and/or anticancer therapy within 2 weeks of study entry (with the exception of hydroxyurea, which is permitted before and during Cycle 1 of therapy until D10, at the discretion of the investigator)

4. Prior treatment with venetoclax, decitabine, or azacitidine

5. Diagnosis of acute promyelocytic leukemia

6. Pregnant or breastfeeding patients

7. Patient known to be positive for HIV

8. Known CNS involvement with AML

9. Evidence of other clinically significant uncontrolled condition(s) including, but not

limited to:

1. Uncontrolled and/or active systemic infection (viral, bacterial or fungal)

2. Chronic hepatitis B virus (HBV) or hepatitis C (HCV) requiring treatment. Note:

subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.

3. An active second cancer that requires treatment within 6 months of study entry

10. Cardiac history including the following:

1. History of CHF requiring treatment or Ejection Fraction = 50%

2. Subject has a cardiovascular disability status of New York Heart Association Class > 2, defined as: i. Cardiac disease in which patients are comfortable at rest but ordinary physical activity ii. Results in fatigue, palpitations, dyspnea, or anginal pain c. Chronic stable angina

11. Treatment with any of the following within 7 days prior to the first dose of study

drug:

1. Steroid therapy for anti-neoplastic intent

2. Moderate or strong cytochrome P450 3A (CYP3A) inducers

12. Administration or consumption of any of the following within 3 days prior to the first

dose of study drug:

1. Grapefruit or grapefruit products

2. Seville oranges (including marmalade containing Seville oranges)

3. Star fruit

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Decitabine
Decitabine will be administered intravenously at a dose of 20mg per day for 10 days during Cycle 1 (28 day cycle) Decitabine will be administered intravenously at a dose of 20mg per day for 10 days of Cycle 2 (28 day cycle). Decitabine will be administered intravenously at a dose of 20mg per day for 5 days of each 28 day maintenance cycle
• Venetoclax
Venetoclax administered orally on days 1-21 of cycle 1, cycle 2 and maintenance (28 day cycles). Dose levels will be assigned at time of enrollment anywhere from 100mg-400mg. Dose escalation will follow the 3+3 study design.

Locations

Country	Name	City	State
United States	University Of Chicago Medicine Comprehensive Cancer Center	Chicago	Illinois

Sponsors (2)

Lead Sponsor	Collaborator
University of Chicago	AbbVie

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The rate of dose limiting toxicity (DLT)	Determine the rate of subjects who experience a dose limiting toxicity and the maximum tolerable dose	24 months
Secondary	Levels of toxicity with combination regimen	Levels of toxicity experienced with the combination regimen will be reported using data summaries of adverse events, dose limiting toxicity and other safety parameters.	24 months
Secondary	Assessment of Overall Survival	Survival will be measured in months from the date of subject enrollment to the date of death.	24 months