Clinical trial · Interventional
Study of IMC-EB10 in Participant With Leukemia
An Open-label, Dose Escalation, Phase I Study of IMC-EB10 in Patients With Relapsed or Refractory Acute Myeloid Leukemia
NCT00887926CI-TRIAL-00062834terminatedPhase 1Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Lack of efficacy
Summary
Brief summary (as posted)
The purpose of this study is to determine if IMC-EB10 is safe for participants with leukemia, and also to determine the best dose of IMC-EB10 to give to participants.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myeloid Leukemia | Myeloid Leukemia | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IMC-EB10 | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- IMC-EB10 5 milligrams/kilogram (mg/kg)
- description
- All participants will receive intravenous infusions of IMC-EB10, with the dose depending on which cohort they are enrolled into.
- interventionNames
- Biological: IMC-EB10
Primary outcomes (1)
- measure
- Maximum Tolerate Dose (MTD) of IMC-EB10
- timeFrame
- Cycle 1 (28-day cycle)
- description
- MTD is defined as the dose preceding the dose level at which 2 participants experienced a dose limiting toxicity (DLT) during Cycle 1. DLT is defined using National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI-CTCAE v 3.0): (1) any Grade 3 or 4 toxicity that is clearly not attributable to leukemia \[for example (e.g.) a type of end-organ failure that is infrequently encountered in acute myeloid leukemia (AML)\] and is possibly, probably, or definitely attributable to IMC-EB10 in the judgment of the investigator; and (2) any Grade 3 or 4 toxicity that is clearly not attributable to a co-medication (e.g., prolonged neutropenia that is not attributable to hydroxyurea).
Secondary outcomes (7)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. The participant has acute myeloid leukemia in the bone marrow or blood that has relapsed with or without a prior complete remission 2. The participant is not regarded to be a candidate for a potentially curative, higher priority treatment for acute myeloid leukemia 3. The participant has resolution of all clinically significant toxic effects of any prior antitumor therapy and any other study-specific clinical or laboratory parameter specified in the entry criteria 4. The participant has not had major surgery, an open biopsy, a significant injury, and/or prior antitumor therapy (except antileukemia therapy) within 21 days prior to the first infusion of IMC-EB10 5. The participant has an Eastern Cooperative Oncology Group (ECOG)performance status of 0, 1, or 2 at study entry. 6. The participant is age 18 years or older 7. The participant has a life expectancy of \>3 months 8. The participant has adequate liver and kidney function, as defined in the entry criteria 9. The participant is using an effective contraception (per the institutional standard), if procreative potential exists 10. The participant is able to give written informed consent 11. The participant is willing and able to comply with study procedures, scheduled visits, and treatment plans Exclusion Criteria: 1. The participant has had prior allogenic or autologous stem cell transplant within \<3 months of the first infusion of IMC-EB10 2. The participant has had an organ transplant (nonhematologic) within 3 years of study entry 3. The participant has active central nervous system leukemia 4. The participant has extramedullary disease without peripheral/and or bone marrow involvement 5. The participant is disease-free from a previous or concurrent malignancy for a period ≤ 1 year. A participant who has basal cell carcinoma or carcinoma in situ of the cervix will not be excluded from the study 6. The participant is currently receiving antileukemia therapy. Concurrent treatment with hydroxyurea is permitted 7. The participant has uncontrolled intercurrent illness as specified in the study entry criteria 8. The participant is receiving chronic steroid or other immunosuppressive medications. Occasional use of steroid-containing medications for, for example (e.g.), asthma exacerbation or for skin lesions, is permitted 9. The participant is receiving full-dose heparin (including low molecular weight heparin) or warfarin. \[The participant is permitted to use low-dose warfarin to maintain patency of preexisting, permanent, indwelling intravenous (I.V.) catheters.\] 10. The participant is pregnant (confirmed by urine or serum pregnancy test) or breast feeding 11. The participant has received treatment with monoclonal antibodies within 6 weeks prior to first infusion of IMC-EB10 12. The participant has a history of clinically significant allergic reactions to monoclonal antibodies or other therapeutic proteins
References
Publications (0)
Data not yet available
No reference posted for this study.