Oral Clofarabine for Acute Myeloid Leukemia

Completed · Phase 1

Conditions studied: Leukemia, Myeloid, Acute

In brief

This is a phase I study designed to test the safety of oral clofarabine when given as consolidation therapy to older patients with AML in remission.

Key facts

Study ID

NCT00727766

Run by

Washington University School of Medicine

People needed

25

Starts

2009-01-01

Expected to finish

2014-11-01

Last updated by the study team

2014-11-11

Who can join

Age: 60 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of Acute Myeloid Leukemia according to WHO criteria
• Age ≥ 60 years at enrollment
• Patients must be in complete remission by bone marrow examination, within 30 days of enrollment, following treatment with a cytotoxic induction chemotherapy regimen (such as 7+3)
• Complete remission must be confirmed by bone marrow biopsy
• If one cycle of consolidation was administered, then patient may be within 60 days of the confirmation of complete remission by bone marrow biopsy
• Minimum platelet count of 100,000
• Patients may have received "low-intensity" therapy (i.e. decitabine, lenalidomide, etc) prior to traditional induction chemotherapy.
• Patients may have received 1 cycle of cytarabine-based consolidation therapy.
• Patients must have an ECOG performance status of 0-2 at the beginning of consolidation therapy.
• Have adequate renal and hepatic functions as indicated by the following laboratory values:
• Serum creatinine ≤ 1.0 mg/dL; if serum creatinine >1.0 mg/dL, then the estimated glomerular filtration rate (GFR) must be >60 mL/min/1.73 m2 as calculated by the Modification of Diet in Renal Disease equation where Predicted GFR (ml/min/1.73 m2) = 186 x (Serum Creatinine)-1.154 x (age in years)-0.023 x (0.742 if patient is female) x (1.212 if patient is black)
• Serum total bilirubin ≤ 1.5 mg/dL × upper limit of normal (ULN) except for unconjugated hyperbilirubinemia secondary Gilbert's syndrome
• Aspartate transaminase (AST)/alanine transaminase (ALT) ≤ 2.5 × ULN
• Alkaline phosphatase ≤ 2.5 × ULN
• Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide signed valid written informed consent or when appropriate, have an appointed legally authorized representative who is capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide signed valid written informed consent for the benefit of the patient.
• Male and female patients who are of child bearing potential must use an effective contraceptive method during the study and for a minimum of 6 months after study treatment.
• Patients MAY have received prior therapy with purine analogs (such as fludarabine and cladribine).

You may not qualify if…

• Current concomitant chemotherapy, radiation therapy, or immunotherapy other than as specified in the protocol.
• The diagnosis of AML-M3 (acute promyelocytic leukemia) characterized by translocations involving the retinoic acid receptor-alpha (RAR-alpha) gene.
• Use of investigational agents within 2 weeks or any anticancer therapy within 2 weeks before study entry. The patient must have recovered from all acute toxicities from any previous therapy.
• Have any other severe concurrent disease, or have a history of serious organ dysfunction or disease involving the heart, kidney, liver, or other organ system that may place the patient at undue risk to undergo treatment.
• Patients with a systemic fungal, bacterial, viral, or other infection not controlled (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment).
• Have currently active gastrointestinal disease, or prior surgery that may affect the ability of the patient to absorb oral clofarabine.

Where it is running

• Washington University — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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