Clinical Trial Finder

Inclusion Criteria:

• - Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2.

• - Adequate organ function (bone marrow, hepatic, renal, cardiovascular) - Left ventricular ejection fraction of ≥50% - Female patients of childbearing potential must have a negative pregnancy test within 7 days of the start of treatment and must agree to use a highly effective method of contraception during the trial.

• - Patients must have recovered from the effects of any prior cancer related therapy, radiotherapy or surgery (toxicity ≤ Grade 1) - All patients on prior investigational agents must wait at least 5 half-lives of the agent in question, or 14 days, whichever is longer before study entry.

• - AML patients only: Pathologically confirmed diagnosis of AML as defined by the WHO Classification and patients with targeted mutations must have been treated with appropriate therapy for their disease.

• - White blood cell count < 25 x 10^9/L.

Hydrea or leukapheresis are permitted to meet this criterion.

• - CMML patients only: intermediate-2 or high risk per CMML-specific prognostic scoring system (CPSS) or clinical/molecular CPSS (CPSS-mol) criteria.

Must have failed prior therapy with a hypomethylating agent.

• - MDS patients only: Intermediate, high, or very high risk by International Prognostic Scoring System-Revised [IPSS-R] criteria that is relapsed or refractory to approved therapies or MDS/MPN Overlap Syndrome (displaying both fibrosis and dysplastic features).

• - NHL patients only: Histologically or cytologically confirmed NHL, including B- and T-cell lymphomas that is relapsed or refractory or intolerant to approved therapies.

Must have one lesion that can be measured for response.

• - MM patients only: Measurable disease defined by one or more of the following: Serum M-protein ≥ 0.5 g/dL, Urine M-protein ≥ 200 mg/24 hours, Serum Free Light Chain (sFLC) > 10 mg/dL with normal serum FLC ratio.

Presence of soft tissue plasmacytoma confirmed by imaging.

• - NHL and MM patients only: must have the following lab values within 14 days prior to study Day 1: - ANC ≥1.0 x 10^3 μL.

• - Platelet count ≥50,000 μL.

Exclusion Criteria:

• - Known hypersensitivity to any of the components of PRT1419.

• - Female patients who are pregnant or lactating.

• - Mean QTcF interval of >480 msec.

• - History of heart failure, additional risk factors for arryhthmias or requiring concomitant medications that prolong the QT/QTc interval.

• - Hematopoietic stem-cell transplant < 90 days or have GVHD Grade >1 at study entry.

• - Uncontrolled intercurrent illnesses.

• - Treatment with strong inhibitors of CYP2C8 and/or P-glycoprotein for which there are no therapeutic substitutions.

• - Inflammatory disorders of the gastrointestinal tract, or subjects with GI malabsorption.

• - HIV positive; known active hepatitis B or C.

• - Prior exposure to an MCL1 inhibitor.

• - History of another malignancy except: - Malignancy treated with curative intent with no known active disease for >2 years at study entry.

• - Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.

• - Adequately treated carcinoma in situ without evidence of disease.

• - Other concurrent low-grade malignancies (i.

e chronic lymphocytic leukemia (Rai 0)) may be considered after consultation with Sponsor.

This is a multicenter, open-label, dose-escalation Phase 1 study of PRT1419, a MCL1 inhibitor, evaluating patients in two cohorts as part of a 28-day treatment cycle in adult patients with multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), acute myeloid leukemia (AML), chronic myelomonocytic leukemia (CMML), high-risk myelodysplastic syndrome (MDS) or MDS/myeloproliferative neoplasm (MPN) overlap syndrome. Cohort A will evaluate PRT1419 administered as monotherapy in patients with either AML, CMML and/or high-risk MDS or MDS/MPN overlap. Cohort B will evaluate PRT1419 administered as monotherapy in patients with NHL or MM. The study will employ a "3+3" dose escalation design. The dose may be escalated until a dose limiting toxicity is identified.

Arms

Experimental: PRT1419

PRT1419 will be administered orally

Interventions

Drug: - PRT1419

PRT1419 will be administered orally