Study of CB-5339 in Acute Myeloid Leukemia or Myelodysplastic Syndrome

NCT04402541 | Completed Phase 1 DMC FDA Drug

• 1 other identifier: CTX-001
• Study Type: interventional
• Target: 55
• Locations: 2 countries
• Sites: 10

Brief Summary

This is a multicenter, open-label Phase 1 study of orally administered CB-5339 in participants with R/R AML or participants with R/R intermediate- to high-risk MDS.

Conditions

Acute Myeloid Leukemia, in Relapse; Myelodysplastic Syndromes

Outcome Measures

Primary Outcomes (2)

• Incidence of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs).

  28 Days

• Define the MTD and/or RP2D and schedule for CB-5339

  Incidence and nature of DLTs with CB-5339 monotherapy for MTD determination. All available safety, efficacy and PK, for RP2D determination

  28 Days

Secondary Outcomes (6)

• Peak plasma concentration (Cmax)

  Day 1 and Day 4

• Time to reach peak plasma concentration (Tmax)

  Day 1 and Day 4

• Area under the plasma concentration time curve (AUC0-t)

  Day 1 and Day 4

• Elimination half-life (t½)

  Day 1 and Day 4

• Accumulation ratio

  Day 1 and Day 4

Study Arms (1)

CB-5339

EXPERIMENTAL

Orally administered CB-5339

Drug: CB-5339

Interventions

CB-5339 DRUG

25mg and 75mg capsules

Also known as: CB-5339 Tosylate

CB-5339

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female and ≥ 18 years of age at the time of signing the consent form
• One of the following advanced hematologic malignancies including:
• Relapsed or refractory AML as defined by 2016 WHO criteria and are not candidates for curative therapies such as allogeneic hematopoietic cell transplant or for whom there is no standard of care therapy available that is likely to lead to disease remission according the investigator
• MDS high-very high risk by the revised international scoring system for evaluating prognosis in myelodysplastic syndromes that is recurrent or refractory or the participant is intolerant to established therapy known to provide clinical benefit for their condition (e.g., relapsed following treatment with hypomethylating agent or lack of response after \> 4 cycles), according to treating physician. Potential participants who meet the criteria for intermediate risk may be considered with approval by the medical monitor if the participant has severe cytopenia(s) and/or elevated bone marrow blast counts.
• Adequate organ function defined as:
• Serum creatinine ≤1.5 mg/dL or an estimated glomerular filtration rate of ≥60 mL/min as calculated by the Cockcroft-Gault glomerular filtration rate equation
• Total bilirubin ≤ 1.5 × the upper limit of normal (ULN) unless considered due to Gilbert's disease or leukemic disease
• Aspartate aminotransferase (AST) ≤3 × the ULN; alanine aminotransferase (ALT) ≤3 × the ULN. Levels of AST and/or ALT ≤5 × the ULN may be acceptable for participants with known leukemic involvement of the liver after discussion with the study medical monitor
• Eastern Cooperative Oncology Group (ECOG) performance status ≤2.
• Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. If of childbearing potential, agree to use an effective barrier method of birth control (i.e., latex condom, diaphragm, cervical cap, etc.) to avoid pregnancy during the study and 90 days after the last dose of CB-5339. Female participants of childbearing potential need a negative serum or urine pregnancy test within 7 days of study enrollment. Non-childbearing is defined as ≥ 1 year postmenopausal or surgically sterilized
• Capable of giving signed informed consent as described in Appendix 1 which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol

You may not qualify if:

• Acute promyelocytic leukemia with t(15;17)(q22;q12); or abnormal promyelocytic leukemia/retinoic acid receptor alpha (PML-RARA).
• Participants with clinical symptoms suggestive of active central nervous system (CNS) leukemia or known CNS leukemia. Evaluation of cerebrospinal fluid is only required if there is a clinical suspicion of CNS involvement by leukemia during screening.
• Participants with immediately life-threatening, severe complications of leukemia such as uncontrolled bleeding, pneumonia with hypoxia or shock, and/or disseminated intravascular coagulation.
• Concomitant malignancy, requiring active treatment, except for basal-cell or squamous cell carcinoma of the skin, carcinoma-in-situ of the uterine cervix, or localized prostate cancer.
• Adjuvant therapy for breast cancer or prostate cancer is allowed.
• Active, uncontrolled, systemic infection or severe localized infection during screening or prior to Cycle 1 Day 1 (C1D1; unless considered due to tumor by the investigator).
• Note, participants receiving prophylactic anti-infectives are allowed on study.
• Known human immunodeficiency virus (HIV) infection with CD4+ T cell counts \<350 cells/μL, initiation of antiretroviral therapy within 4 weeks before C1D1, or acquired immunodeficiency syndrome (AIDS)-related infection within 12 months before C1D1.
• Hepatitis B virus (HBV) or hepatitis C virus (HCV) infection with viral load above the limit of quantification
• Major cardiac abnormalities as defined but not limited to the following: uncontrolled angina or unstable life-threatening arrhythmias, history of myocardial infarction within 12 weeks prior to Baseline, Class 3 or higher New York Heart Association (NYHA) congestive heart failure, or left ventricular ejection fraction (LVEF) \<45% as measured by echocardiogram (ECHO) within 28 days of C1D1
• Persistent (3 consecutive ECGs performed ≥5 minutes apart) prolongation of the corrected QT interval by Fredericia's method (QTcF) to \> 480 msec
• Gastrointestinal conditions that may interfere with the absorption of orally-administered drugs including but not limited to short gut syndrome, gastroparesis, inflammatory bowel disease, or acute pancreatitis.
• Any other severe, acute, or chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation or CB-5339 administration, may interfere with the informed consent process and/or with compliance with the requirements of the study, may interfere with the interpretation of the study results and, in the Investigator's opinion, or would make the participant inappropriate for entry into this study
• A condition that is expected to require concomitant use of any medication listed as prohibited while on study.
• Known hypersensitivity to any components of CB-5339.

Sponsors & Collaborators

• Cleave Therapeutics, Inc.: lead

Study Sites (10)

USC Norris Comprehensive Cancer Center

Los Angeles, California, 90033, United States

Location

KU Clinical Research Center

Fairway, Kansas, 66205, United States

Location

Memorial Sloan Kettering Cancer Center

New York, New York, 10021, United States

Location

Weill Cornel Medical Center

New York, New York, 10065, United States

Location

Saint Francis Hospital Cancer Center

Greenville, North Carolina, 29607, United States

Location

Cleveland Clinic, Case Comprehensive Cancer Center

Cleveland, Ohio, 44122, United States

Location

MD Anderson Cancer Cancer

Houston, Texas, 77030, United States

Location

St. Vincent Hospital, Sydney, NSW

Darlinghurst, New South Wales, 2010, Australia

Location

Epworth Healthcare

Melbourne, Victoria, 3002, Australia

Location

Haematology Clinical Trials Unit, Royal Perth Hospital

Perth, Western Australia, 6000, Australia

Location

Related Publications (1)

• Wang F, Li S, Rosencrans WM, Cheng KW, Stott GM, Mroczkowski B, Chou TF. Sulforaphane is Synergistic with CB-5083 and Inhibits Colony Formation of CB-5083-Resistant HCT116 Cells. ChemMedChem. 2022 Jun 3;17(11):e202200030. doi: 10.1002/cmdc.202200030. Epub 2022 Apr 22.

  PMID: 35451199 DERIVED

MeSH Terms

Conditions

Leukemia, Myeloid, Acute; Myelodysplastic Syndromes

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases; Bone Marrow Diseases

Study Officials

• Scott Harris

  Cleave Therapeutics, Inc.

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 18, 2020
• First Posted: May 27, 2020
• Study Start: June 8, 2020
• Primary Completion: July 23, 2023
• Study Completion: July 23, 2023
• Last Updated: August 31, 2023

Record last verified: 2023-08

Locations

AU (3); US (7)