Clinical Trial 24018

• Overview

  Study Title:

  A Phase Ib study of Rezatapopt in combination with Azacitidine in patients with Relapsed/Refractory TP53Y220C mutant myeloid malignancies (Acute Myeloid Leukemia or Myelodysplastic syndrome)

  Summary:

  A non-randomized phase Ib study of PC14586 (PMV therapeutics) in patients diagnosed with TP53Y220C-mutant myeloid malignancies, including AML and MDS.

  Objective:

  Primary Objective: To assess the safety and tolerability of rezatapopt alone and in combination with AZA in patients with TP53Y220C-mutant myeloid malignancies (AML, MDS). Secondary Objectives: a) To determine the clinical efficacy of rezatapopt alone and in combination with AZA in R/R patients with TP53Y220C -mutant myeloid malignancies. b) To assess event free survival (EFS) and overall survival (OS). c) To assess duration of response in responding patients. d) Characterize the pharmacokinetics of rezatapopt in patients with myeloid malignancies.

• Treatments

  Therapies:

  BCL-2 inhibitor; DNA methyltransferase inhibitor

  Medications:

  Azacitidine (); Rezatapopt ()

• Inclusion Criteria

  Key Inclusion Criteria:
  • Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF).
  • Patient is willing and able to adhere to the study visit schedule and other protocol requirements.
  • Patient has relapsed or primary refractory AML or MDS
  • Any other comorbidity that per the investigator renders a patient inappropriate for intensive chemotherapy.
  • Patients with MDS must be classified as MDS-IB1 or IB2 as per WHO 2022 criteria32
  • TP53Y220C mutation confirmed by CLIA-approved local testing with a variant allele frequency >2%.
  • Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of ≤2
  • Patient has adequate organ function
  • Females of childbearing potential may participate provided they have a negative serum or urine pregnancy test at screening and a negative serum OR urine pregnancy test within 72 hours of starting on treatment. They also must agree to either abstain from sexual intercourse or use two forms of a highly effective method of contraception while on study and up to 3 months after the last dose of the study drug.
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) 14 days prior to study entry and for the duration of study participation.
  • Ability to understand and the willingness to sign a written informed consent document.

• Exclusion Criteria

  Key Exclusion Criteria:
  • Patient has received prior chemotherapy, targeted therapy, immunotherapy, or treatment with an investigational anticancer agent within 14 days or 5 half-lives (if half-life is known), whichever is shorter, before receiving their first dose of study drug.
  • Patient has received radiotherapy within 14 days.
  • Patients with acute promyelocytic leukemia.
  • Subject has immediate life-threatening, severe complications of leukemia such as uncontrolled bleeding, pneumonia with hypoxia or shock, and/or disseminated intravascular coagulation.
  • Patients with active, uncontrolled leukemia involvement of the CNS.
  • Subject has known active viral infection with human immunodeficiency virus (HIV), or active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV).
  • Subject is known to have dysphagia, short-gut syndrome, gastroparesis, or other conditions that limit the ingestion or gastrointestinal absorption of drugs administered orally.
  • Subject has active uncontrolled systemic fungal, bacterial, or viral infection (defined as ongoing signs/symptoms related to the infection without improvement despite appropriate antibiotics, antiviral therapy, and/or other treatment).
  • Patient has any unresolved toxicities from prior anti-cancer therapy greater than Grade 1 at the time of starting study treatment with the exception of alopecia and Grade 2 prior chemotherapy induced neuropathy.
  • Patient has had major surgery within 2 weeks prior to the planned start of study treatment.
  • Female subject who is pregnant or lactating.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to azacitidine, rezetapopt or other agents used in study.

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