Study of AZD5991 alone or in combination with venetoclax in relapsed or refractory haematologic malignancies.

Exclusion Criteria

• (AZD5991 + venetoclax):
• • Treatment with any of the following:
• o Any investigational agents from a previous clinical study within 4 half-lives or 14 days, whichever is the greater, of said prior investigational agent(s) with regard to the first dose of study treatment on this protocol. Washout period not required in subjects with aggressive disease who require treatment sooner.
• o Any other chemotherapy, immunotherapy or anticancer agents within 2 weeks of the first dose of study treatment. Washout period not required in subjects with aggressive disease who require treatment sooner.
• o Any hematopoietic growth factors (eg, filgrastim [granulocyte colony-stimulating factor; G-CSF], sargramostin [granulocyte-macrophage colony-stimulating factor; GM-CSF]) within 7 days of the first dose of study drug or pegylated G-CSF (pegfilgrastim) or darbepoetin within 14 days of the first dose of study drug.
• o Major surgery (excluding placement of vascular access) within 4 weeks of the first dose of study treatment.
• • Except for alopecia, any unresolved toxicities from prior therapy greater than CTCAE Grade 1 at the time of starting study treatment.
• • AML with known active central nervous system involvement.
• • As judged by the Investigator, any evidence of severe or uncontrolled systemic disease (eg, severe hepatic impairment, interstitial lung disease [bilateral, diffuse, parenchymal lung disease]), or current unstable or uncompensated respiratory or cardiac conditions, or uncontrolled hypertension, history of, or active, bleeding diatheses (eg, hemophilia or von Willebrand disease) or uncontrolled active systemic fungal, bacterial, viral, or other infection (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment), or intravenous anti-infective treatment within 2 weeks before first dose of study drug.
• • Malabsorption syndrome or other condition that precludes enteral route of administration.
• • Chronic respiratory disease that requires continuous oxygen use.
• • Known diagnosis of a hypercoagulable disorder other than malignancy
• • Undergone any of the following procedures or experienced any of the following conditions currently or in the preceding 6 months:
• o angina pectoris
• o supraventricular arrhythmias, including atrial fibrillation, which are uncontrolled
• o Myocarditis
• o heart failure NYHA Class I or above
• • Experienced any of the following conditions currently or at any previous timepoint
• o Myocardial infarction (MI)
• o coronary artery bypass graft
• o angioplasty
• o vascular stent
• o Heart failure NYHA Class ≥ 2
• o Ventricular arrhythmias requiring continuous therapy
• • Any of the following cardiac criteria:
• o Mean resting corrected QT interval (QTcF) ≥ 450 msec applicable to both genders obtained from 3 electrocardiograms (ECGs) (averaged)
• o Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG eg, complete left bundle branch block, second to third degree AV block, sinus node dysfunction with clinically significant sinus pause
• o Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalaemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age. Concomitant medications known to prolong QTc should be used with caution and cannot be used starting with the first dose of study drug and through the DLT review period.
• o ST-wave depression and T-wave changes (e.g. inversion or flattened) in recent or screening ECG
• o CPK assay reading ≥ ULN at screening
• o Subjects with any troponin assay reading of ≥ULN during screening
• o Left ventricular ejection fraction [LVEF] <55% with echocardiogram (ECHO) or multi-gated acquisition scan (MUGA). Appropriate correction to be used, if a MUGA is performed.
• • History of severe allergic or anaphylactic reactions to BH3 mimetics or history of hypersensitivity to active or inactive excipients of AZD5991.
• • Received the following within 7 days before initiation of venetoclax:
• • Strong or moderate cytochrome P450 3A (CYP3A) inducers
• • Strong or moderate CYP3A inhibitors
• • Pg-P inhibitors
• • Consumed grapefruit, grapefruit products, Seville oranges (including marmalade containing Seville oranges) or star fruit within 3 days before the initiation of venetoclax.