Clinical Trial Finder

Inclusion Criteria:

1. Participants with post HMA-failure high-risk MDS (Int-2 or high risk by the IPSS with overall score >/=1.5) with excess blasts >5% with failure defined as prior receipt of 4 cycles of HMA therapy with failure to attain a response, or progression of disease or relapse at any time after prior response to HMA therapy. 2. Participants with relapsed/refractory chronic myelomonocytic leukemia (CMML) and therapy-related MDS are also eligible. 3. Hydroxyurea is allowed to lower the white cell count /= 18 years of age. 10. ECOG/PS ≤2.

Exclusion Criteria:

1. Participants having received any prior BCL2 inhibitor therapy. 2. Participants with MDS with IPSS risk categories Low or Int-1 (overall IPSS score < 1.5). 3. Participants with known HIV infection (due to potential drug-drug interactions between antiretroviral medications and venetoclax). HIV testing will be performed at screening, only if required per local guidelines or institutional standards. 4. Participants known to be positive for hepatitis B or C infection [HCV Ab indicative of a previous or current infection; and/or positive HBs Ag or detected sensitivity on HBV-DNA PCR test for HBc Ab and/or HBs Ab positivity] with the exception of those with an undetectable viral load within 3 months of screening. (Hepatitis B or C testing is not required). Subjects with serologic evidence of prior vaccination to HBV [i.e., HBs Ag-, and anti-HBs+] may participate. 5. Participants has received strong and/or moderate CYP3A inducers within 7 days prior to the initiation of study treatment. 6. Participants has consumed grapefruit, grapefruit products, Seville oranges (including marmalade containing Seville oranges) or Starfruit within 3 days prior to the initiation of study treatment. 7. Participants has a cardiovascular disability status of New York Heart Association Class > 2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea, or anginal pain. 8. Participant has chronic respiratory disease that requires continuous oxygen, or significant history of renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic, hepatic, cardiovascular disease, any other medical condition or known hypersensitivity to any of the study medications including excipients of azacitidine that in the opinion of the investigator would adversely affect his/her participating in this study. 9. Participant has a malabsorption syndrome or other condition that precludes enteral route of administration. 10. Participant exhibits evidence of other clinically significant uncontrolled systemic infection requiring therapy (viral, bacterial or fungal). 11. Participant has received a live attenuated vaccine within 4 weeks prior to the first dose of study drug. 12. Participant has a history of other malignancies within 2 years prior to study entry, with the exception of:

• - Adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of breast; - Basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin; - Previous malignancy confined and surgically resected (or treated with other modalities) with curative intent; requires discussion with TA MD.

13. Participant has a white blood cell count > 10 × 109/L. (Hydroxyurea or leukapheresis are permitted to meet this criterion) 14. Female subject has positive results for pregnancy test. 15. Participants with (Grade > 1) unresolved from prior treatment (including chemotherapy, targeted therapy, immunotherapy, experimental agents, radiation, or surgery)

PRIMARY OBJECTIVE:

• I. To determine the safety and tolerability (phase 1) and overall response rate (ORR) (phase 2) of venetoclax in combination with azacitidine in patients with high risk myelodysplastic syndrome (MDS) or chronic myelomonocytic leukemia (CMML) with bone marrow excess blasts > 5% that are relapsed/refractory to prior hypomethylating agent (HMA) therapy.

SECONDARY OBJECTIVES:

• I. Rate of complete remission (CR).

• II. Rate of marrow/morphologic complete remission (mCR).

• III. Rate of hematologic improvement (HI; erythroid/platelet/neutrophil responses).

• IV. Rate of red blood cell (RBC) transfusion independence.

• V. Rate of platelet (PLT) transfusion independence.

• VI. Rate of cytogenetic response.

• VII. Rate of bone marrow blast response.

• VIII. Time to transformation to acute myeloid leukemia (AML).

• IX. Duration of response (DOR).

• X. Overall survival (OS).

XI. Progression-free survival (PFS). XII. Time to next MDS treatment (TTNT). XIII. Event-free survival (EFS). EXPLORATORY OBJECTIVE:

• I. To investigate the effects of therapy on MDS and to identify biological markers of response to venetoclax and/or its combination with azacitidine.

OUTLINE: This is a phase I, dose-escalation study of venetoclax followed by a phase II study. Patients receive venetoclax orally (PO) daily on days 1-14 and azacitidine intravenously (IV) over 15 minutes or subcutaneously (SC) on days 1-5. Cycles repeat every 4-8 weeks in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up within 30 days and then every 3-6 months for up to 5 years.

Arms

Experimental: Treatment (venetoclax, azacitidine)

Patients receive venetoclax PO daily on days 1-14 and azacitidine IV over 15 minutes or SC on days 1-5. Cycles repeat every 4-8 weeks in the absence of disease progression or unacceptable toxicity.

Interventions

Drug: - Azacitidine

Given IV or SC

Drug: - Venetoclax

Given PO