Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California and other locations
Dates
study started
completion around
Principal Investigator
by Gary J. Schiller, MD
Headshot of Gary J. Schiller
Gary J. Schiller

Description

Summary

Phase 1b Study of R289 in Patients with Lower-risk Myelodysplastic Syndromes (LR MDS)

Official Title

An Open-label, Phase 1b Study of R289, an IRAK1/4 Inhibitor, in Patients With Lower-risk Myelodysplastic Syndromes (LR MDS) Who Are Relapsed/Refractory/Resistant to Prior Therapies

Details

An open-label, Phase 1b study of R289, an IRAK 1/4 Inhibitor, to determine tolerability and preliminary efficacy in patients with LR MDS who are relapsed/refractory/resistant, intolerant, or have inadequate response to prior therapies such as erythropoietin (EPO), luspatercept, or hypomethylating agents (HMAs) for MDS.

Keywords

Low Risk Myelodysplastic Syndromes, MDS, LR MDS, Myelodysplastic Syndromes, Hematology Oncology, Hem/ Onc, Preleukemia, Syndrome, R906289 Monosodium (R289 Na)

Eligibility

You can join if…

Open to people ages 18 years and up

  • Patient must be ≥ 18 years of age at the time of signing the informed consent.
  • Must have definitive diagnosis of MDS with very low, low, or intermediate-1 risk (International Prognostic Scoring System (IPSS)-R ≤ 3.5) and ≤5% bone marrow myeloblasts.
  • Must be relapsed, refractory/resistant, intolerant, or have inadequate response to therapies with known clinical benefits for MDS, such as EPOs, luspatercept, and HMAs(i.e., azacytidine or decitabine). Patients with del (5q) must have failed prior lenalidomide therapy.
  • Symptomatic anemia untransfused with hemoglobin < 9.0 g/dL and no RBC transfusion within 16 of registration or
  • RBC transfusion dependent defined as receiving ≥ 2 units of packed red blood cells (PRBCs) within 8 weeks in the preceding 16 weeks for a hemoglobin <9.0 g/dL.
  • Exploratory Phase 1B Cohort:
    1. Transfusion-dependent LR-MDS who are refractory or intolerant to, or are ineligible for ESAs.
    2. No prior therapy with any approved or investigational therapies for MDS
    3. No del 5q cytogenetic abnormality
    4. RBC transfusion dependent defined as receiving ≥ 2 units of PRBCs within 8 weeks in the preceding 16 weeks for a hemoglobin <9.0 g/dL
  • All participants must have documented marrow iron stores. If marrow iron stain is not available, the transferrin saturation must be >20% or a serum ferritin > 100ng/100mL
  • Must have Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2 at screening.
  • Must have adequate organ function, defined as:
    1. Hepatic function:
      • aspartate amino transferase (AST) and alanine aminotransferase (ALT) ≤ 1.5 × upper limit of normal (ULN)
      • total bilirubin ≤ 1.5 × ULN
    2. Renal function defined as creatinine clearance > 60 mL/min (using Cockcroft-Gault), or blood creatine < 1.5 mg/dL

You CAN'T join if...

  • Prior treatment for MDS (i.e., TPOs, EPOs, luspatercept, HMAs) concluded < 4 weeks prior to study treatment
  • Clinically significant anemia resulting from iron, B12 or folate deficiencies, autoimmune or hereditary hemolysis, or GI bleeding.
  • MDS secondary to treatment with radiotherapy, chemotherapy, and/or immunotherapy for malignant or autoimmune diseases.
  • Diagnosis of chronic myelomonocytic leukemia.
  • History of uncontrolled seizures.
  • Uncontrolled bacterial or viral infection (i.e., documented HIV, hepatitis B or hepatitis C).
  • History of an active malignancy within the past 2 years prior to study entry, with the exception of:
    1. Adequately treated in situ carcinoma of the cervix uteri
    2. Adequately treated basal cell carcinoma or localized squamous cell carcinoma of the skin, or
    3. Low grade, early-stage prostate cancer (Gleason score 6 or below, stage 1 or 2) with no requirement for therapy at any time prior to the study, or previously resected.
  • History of or active, clinically significant, cardiovascular, respiratory, GI, renal, hepatic, neurological, psychiatric, musculoskeletal, genitourinary, dermatological, or other disorder that, in the Investigator's opinion, could affect the conduct of the study or the absorption, metabolism or excretion of the study treatment.
  • Prior history of autologous or allogeneic stem cell transplantation
  • Marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval > 480 milliseconds [msec]) (Common Terminology Criteria for Adverse Events [CTCAE] Grade 1) using Fridericia's QT correction formula.
  • History of additional risk factors for TdP (e.g., symptomatic heart failure with left ventricular ejection fraction [LVEF] <40%, hypokalemia, family history of Long QT Syndrome).
  • Receiving any other concurrent chemotherapy, radiotherapy, or immunotherapy (within 2 weeks of initiating study treatment), or the toxicity of the relevant prior treatment has not been resolved yet.
  • Use of concomitant medications that prolong the QT/QTc interval during study treatment
  • Use of concomitant medications that are strong CYP3A or CYP2B6 inhibitors or inducers during study treatment

Locations

  • University of California, Los Angeles accepting new patients
    Los Angeles California 90095 United States
  • University of California, Irvine accepting new patients
    Orange California 92868 United States

Lead Scientist at UCLA

  • Gary J. Schiller, MD
    Professor-in-Residence, Medicine. Authored (or co-authored) 163 research publications

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Rigel Pharmaceuticals
Links
Sign up for this study
ID
NCT05308264
Phase
Phase 1/2 Myelodysplastic Syndrome Research Study
Study Type
Interventional
Participants
Expecting 86 study participants
Last Updated