CPI-613 and Hydroxychloroquine for Patients With High Risk Myelodysplastic Syndrome

Withdrawn before enrolling · Phase 1/Phase 2

Conditions studied: Myelodysplastic Syndromes, Progressive Disease

In brief

This is a phase 1/2 study of the combination of CPI-613 and hydroxychloroquine for the treatment of high risk myelodysplastic syndrome patients who have failed a hypomethylating agent.

Key facts

Study ID

NCT03929211

Run by

Wake Forest University Health Sciences

People needed

0

Starts

2021-05-01

Expected to finish

2027-07-01

Last updated by the study team

2021-04-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must meet all of the following inclusion criteria before enrollment:
• Histologically documented high risk MDS whose disease has failed to respond, progressed or relapsed while on a hypomethylating agent.
• IPSS-R score of Intermediate, high or very high at time of enrollment
• ECOG Performance Status of ≤3.
• Men and women 18 years of age or older.
• Expected survival >2 months.
• Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use accepted contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device) during the study, and must have a negative serum or urine pregnancy test within 1 week prior to treatment initiation.
• Fertile men must practice effective contraceptive methods during the study, unless documentation of infertility exists.
• Patients must have fully recovered from the acute, non-hematological, non-infectious toxicities of any prior treatment with cytotoxic drugs, radiotherapy or other anti-cancer modalities. Patients with persisting, non-hematologic, non-infectious toxicities from prior treatment ≤ Grade 2 are eligible, but must be documented as such.
• Laboratory values obtained ≤2 weeks prior to enrollment must demonstrate adequate hepatic function, renal function, and coagulation as defined below:
• Aspartate aminotransferase [AST/SGOT] ≤3x upper normal limit [UNL]
• Alanine aminotransferase [ALT/SGPT] ≤3x UNL
• Bilirubin ≤1.5x UNL
• Serum creatinine ≤1.5 mg/dL or 133 μmol/L
• Albumin ≥ 2.0 g/dL or ≥ 20 g/L.
• Mentally competent, ability to understand and willingness to sign an IRB-approved written informed consent form.
• Have access via central line (e.g., portacath).

You may not qualify if…

• Patients with the following characteristics are excluded:
• Serious medical illness, such as significant cardiac disease (e.g. symptomatic congestive heart failure, unstable angina pectoris, symptomatic coronary artery disease, myocardial infarction within the past 3 months, uncontrolled cardiac arrhythmia, pericardial disease or New York Heart Association Class III or IV), or severe debilitating pulmonary disease, that would potentially increase patients' risk for toxicity.
• Patients with active central nervous system (CNS) or epidural tumor.
• Any active uncontrolled bleeding or bleeding diathesis (e.g., active peptic ulcer disease).
• Any condition or abnormality which may, in the opinion of the investigator, compromise his or her safety.
• Pregnant women, or women of child-bearing potential not using reliable means of contraception.
• Fertile men unwilling to practice contraceptive methods during the study period.
• Lactating females.
• Life expectancy less than 2 months.
• Unwilling or unable to follow protocol requirements.
• Evidence of ongoing uncontrolled serious infection.
• Requirement for immediate palliative treatment of any kind including surgery.
• Patients with uncontrolled HIV infection. (Note: Patients with known HIV infection are excluded because patients with an immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy, and because there may be unknown or dangerous drug interactions between CPI-613 and anti-retroviral agents used to treat HIV infections).
• Patients who have received radiotherapy, surgery, treatment with cytotoxic agents (except a hypomethylating agent, i.e. azacytidine or decitabine), treatment with biologic agents, immunotherapy, or any other anti-cancer therapy of any kind, or any other standard or investigational treatment for their cancer, or any other investigational agent for any indication, within the past 2 weeks prior to initiation of CPI-613 treatment.
• Patients that have received a chemotherapy regimen with stem cell support in the previous 6 months.

Where it is running

• Roswell Park Cancer Institute — Buffalo, New York, United States
• Wake Forest Baptist Comprehensive Cancer Center — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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