New hope for kids with hard-to-treat leukemia: experimental combo shows promise
NCT ID NCT01279096
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new combination of chemotherapy drugs for children and young adults with acute lymphoblastic leukemia (ALL) that had returned or not responded to first treatment. The goal was to find the safest dose of clofarabine when given with other medicines. Twenty participants were enrolled to see if the combination could help them achieve remission without causing severe side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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20 people
The number who actually took part.
- Start date
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Jan 2010
- Finished
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Jun 2013
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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1 year to 23 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 1 to 21 years old at the date of acute lymphoblastic leukemia initial diagnosis * Very early medullary first relapse occurring during the first 18th months after complete remission OR patients with second relapse OR a relapse occurring 6 months or more after myeloablative stem cell transplantation will be eligible. * Have a Karnofsky Performance Status (KPS) of ≥70 for patients \>10 years of age or a Lansky Performance Status (LPS) of ≥60 for patients ≤10 years of age. * No concomitant malignant disease. * No active uncontrolled infection. * Have adequate renal and hepatic functions * absence of concomitant severe cardiovascular disease, i.e. congestive heart failure * Female patients of childbearing potential must have a negative serum pregnancy test within 2 weeks prior to enrollment. * Male and female patients must use an effective contraceptive method during the study and for a minimum of 6 months after study treatment. Exclusion Criteria: * Current concomitant chemotherapy, radiation therapy, or immunotherapy other than as specified in the protocol. * Use of any investigational agent within 30 days. * Known hypersensitivity to clofarabine or excipients. * Known hypersensitivity to mitoxantrone, etoposide or excipients. * Allergy to both E Coli-Asparaginase and Erwinia Asparaginase * Prior transplant less than 6 months ago. * Trisomy 21 * 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). * Pregnant or lactating patients. * Any significant concurrent disease, illness, or psychiatric disorder that would compromise patient safety or compliance, interfere with consent, study participation, follow up, or interpretation of study results.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Besançon University Hospital
Besançon, 25000, France
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Lille University Hospital
Lille, 59037, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.