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Active, not recruiting Phase 1

RAD001 in Combination With PKC412 in Patients With Relapsed, Refractory or Poor Prognosis AML or MDS

NCT00819546 · tracked via the Priya Life Science Israel tracker
Sponsor
Richard Stone, MD
Phase
Phase 1
Started
2009-01
Last updated
2026-03-25

Condition(s) studied

Acute Myeloid LeukemiaMyelodysplastic Syndrome

Investigational drug(s) / intervention(s)

RAD001 →PKC412 →

RAD001: Participants will receive RAD001 on day 1 at the dose specified then again on days 8-28 for the first cycle. For all subsequent cycles RAD001 will be taken once daily.

PKC412: 50mg orally twice a day on days 2-28 for the first cycle. For all subsequent cycles 50mg of PKC412 will be taken orally twice daily.

Study summary

The purpose of this research study is to determine the safety of the combination of RAD001 and PKC412 as a cancer treatment, and to establish the highest dose of RAD001 that can be given in conjunction with PKC412. These drugs have been used in other research trials for individuals with solid and hematology malignancies. Past research on PKC412 shows that it blocks the abnormal functioning of an enzyme called FLT3. FLT3 is found in your cells in either a normal (wild type) or genetically changed form and plays a role in the survival and growth of AML cells. RAD001 is an inhibitor of a central growth pathway that involves the protein MTOR. The MTOR pathway is overactive in cancer cells, causing the cells to grow abnormally. By inhibiting the abnormal growth activity of the MTOR pathway, RAD001 slows down and possibly stops the growth of cancer cells.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Cytopathologically or histopathologically confirmed diagnosis of AML, MDS (RAEB-1, -2) or CMML, who are either relapsed or refractory to standard therapy, or are considered inappropriate candidates for standard therapy. * Inappropriateness for standard therapy requires a) MDS patients: not be a candidate for immediate allogeneic stem cell transplantation, not have a -5q-cytogenetic abnormality (unless previously received lenalidomide), and not be an appropriate candidate for a DNA hypomethylating agent b) AML patients must be 60 years of age or greater and have one of more of the following documented poor risk factors: ECOG Performance Status = 2, 70 years of age or older, unfavorable cytogenetics. * Life expectancy of at least 12 weeks * Not likely to require cytoreductive therapy within one month (other than hydroxyurea) * ECOG Performance Status of 2 or less * Serum transaminase activity (AST/SGOT \& ALT/SGPT) \< 2.5 x ULN * Serum total bilirubin \< 1.5 x ULN ( with the exception of individuals with Gilbert's disease) * INR \< 1.3 (or \< 3 on anticoagulants) * Fasting serum cholesterol 300mg/dl or 7.75 mmol/L or less AND fasting triglycerides 2.5 ULN or less Exclusion Criteria: * Prior allogeneic, syngeneic, or autologous bone marrow transplant or stem cell transplant less than 2 months previously * Female patients who are pregnant or breast feeding or adults of child bearing not employing double barrier contraception * Concurrent severe and/or uncontrolled medical or psychiatric condition which may interfere with the completion of the study * Impairment of gastrointestinal function or GI disease that may significantly alter absorption of PKC412 or RAD001 * Uncontrolled active infection * Any pulmonary infiltrate on teh baseline chest x-ray known to be new in the previous 4 weeks * Patients with a Grade 2 or higher hypercholesterolemia or hypertriglyceridemia despite lipid-lowering therapy * Patients with history of another malignancy within the past 5 years, with the exception of adequately treated basal or squamous cell skin carcinoma or cervical carcinoma in situ * History of non-compliance to medical regimens and patients who are unwilling or unable to comply with this protocol * Prior treatment with any investigational drug within preceding 4 weeks * Chronic treatment with systemic steroids or another immunosuppressive agent * Patients should not receive immunization with attenuated live vaccines within one week of study entry or during study period * Any severe or uncontrolled medical conditions or other conditions that could affect their participation * Known history of HIV seropositivity * Known hypersensitivity to RAD001 or other rapamycins or to its excipients * Known hypersensitivity to PKC412 or to its excipients * Diagnosis of acute promyelocytic leukemia

Primary outcome measure(s)

  • To identify the maximum tolerated dose of RAD001 that can be given in combination with twice daily PKC412 in patients who are non-chemotherapy candidates with AML or MDS. — 2 years

Trial sites (3)

FacilityCityRegionStatus
Massachusetts General Hospital Boston Massachusetts
Dana-Farber Cancer Institute Boston Massachusetts
Beth Israel Deaconess Medical Center Boston Massachusetts
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT00819546 on ClinicalTrials.gov ↗ ← All trials in Israel