A Multiple Dose, Dose Escalation Trial of AEB1102 in Patients With AML or MDS (NCT02732184) | Clinical Trial Compass
CompletedPhase 1
A Multiple Dose, Dose Escalation Trial of AEB1102 in Patients With AML or MDS
United States, Canada21 participantsStarted 2016-08-15
Plain-language summary
This is the first study of the safety of increasing dose levels of AEB1102 in patients with Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome. The study will also evaluate the amounts of AEB1102 in blood, the effects of AEB1102 on blood amino acid levels and the antitumor effects of AEB1102.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Willing and able to provide informed consent
* Age 18 and older
* Diagnosis of AML or MDS according to the WHO criteria
* AML relapsed or refractory to at least one attempt at induction or subjects not candidates for aggressive induction regimens
* MDS refractory to treatment with HMA therapy or with recurrence or progression of MDS following a response to an HMA
* Has adequate organ function: AST and ALT \< 3X the ULN, serum bilirubin \< 2X the ULN, serum creatinine of \< 2 mg/dL, or a calculated creatinine clearance of \> 50 mL/minute
* ECOG Performance Score of 0 -2
* Recovered from the effects of any prior systemic therapy, radiotherapy or surgery
* Willing to use physician approved birth control method
Exclusion Criteria:
* Current CNS Leukemia
* Acute promyelocytic leukemia or AML with a t(15;17) (q22;q12) cytogenetic abnormality or Bcr/Abl positive leukemia
* \< 60 days from ASCT; has chronic graft-versus host disease (GVHD) or requires continued treatment with systemic immunosuppressive agents
* Uncontrolled infection
* Known HIV, hepatitis B or hepatitis C.
* Other active malignancy that requires therapy
* If female, is lactating or breast feeding
* Hypersensitivity to PEG or other component of AEB1102 (Co-ArgI-PEG)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Maximum Tolerated Dose and Recommended Phase 2 Dose