A Phase 1/2 interventional study of Ipilimumab in Relapsed/Refractory Multiple Myeloma, sponsored by Memorial Sloan Kettering Cancer Center. Terminated at 7 sites in United States. Open to participants aged 21 Years to 73 Years. Per ClinicalTrials.gov, last updated 2023-03-23.
Sponsored by Memorial Sloan Kettering Cancer Center · Phase 1/2, Interventional, and Treatment
This study will test the safety of ipilimumab to see what effects, if any, the drug has when used as maintenance therapy for people with relapsed/refractory multiple myeloma who have received chemotherapy and allogeneic hematopoietic stem cell transplant (AHCT). The investigators also want to find out whether giving ipilimumab after chemotherapy and AHCT is a better way to control the multiple myeloma than chemotherapy and AHCT alone.
3,632 studies on the registry are indexed under Multiple Myeloma; 745 are open to participants now.
This study's enrollment of 3 is below the median of 41 across 2,907 interventional studies indexed under Multiple Myeloma.
Browse Multiple Myeloma studies →Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 328 are open to participants now.
Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.
Counted across the registry records on this site, refreshed daily.
Inclusion Criteria:
Inclusion Criteria prior to Allogeneic Hematopoietic Stem Cell Transplantation (alloHSCT):
Diagnosis of relapsed refractory multiple myeloma defined as more than 2 lines of prior therapy with at least a very good partial remission to most recent salvage therapy.
Note:. A line of therapy is treatment between diagnosis and progression or between two progressions
Patients must have adequate organ function measured by:
Hepatic:
Inclusion Criteria prior to Ipilimumab:
Engraftment of all cell lines without transfusion dependence, defined as:
Exclusion Criteria:
Exclusion Criteria prior to Allogeneic Hematopoietic Stem Cell Transplantation (alloHSCT):
Patients ineligible for therapy with ipilimumab, for example:.
Exclusion Criteria prior to Ipilimumab:
Active immune suppression, defined as:
The patient will be admitted to a single room on the Adult Transplantation Service and allogeneic CD34-selected PBSC or marrow transplantation performed as per MSKCC adult BMT guidelines. Patients will be evaluated at approximately day 100 (±2 weeks) after allo-HSCT.
Drug: Ipilimumab
Ipilimumab 3 mg/kg every 3 weeks for 4 doses.
Phase I: Maximum Tolerated Dose of Ipilimumab
A maximum of 12 patients will be accrued and DLTs will be assessed in these patients. If any DLT is observed in more than one of the six patient cohort, a lower dose of ipilimumab will be evaluated in a new six patient cohort.
Time frame: 1 year
Phase II: Progression Free Survival (PFS)
criteria of the International Myeloma Working Group
Time frame: 2 years
| Milestone | Ipilimumab After Stem Cell Transplantation |
|---|---|
| Started | 3 |
| Completed | 3 |
| Not completed | 0 |
A maximum of 12 patients will be accrued and DLTs will be assessed in these patients. If any DLT is observed in more than one of the six patient cohort, a lower dose of ipilimumab will be evaluated in a new six patient cohort.
No measurements were reported for this outcome.
criteria of the International Myeloma Working Group
No measurements were reported for this outcome.
Collected over up to a year. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Ipilimumab After Stem Cell Transplantation | 1/3 (33.3%) | 0/3 (0%) | 0/3 (0%) |
| Age, Continuous(years) | Ipilimumab After Stem Cell Transplantation |
|---|---|
| Median | 62 (59 to 66) |
| Sex: Female, Male(Participants) | Ipilimumab After Stem Cell Transplantation |
|---|---|
| Female | 0 |
| Male | 3 |
| Ethnicity (NIH/OMB)(Participants) | Ipilimumab After Stem Cell Transplantation |
|---|---|
| Hispanic or Latino | 0 |
| Not Hispanic or Latino | 3 |
| Unknown or Not Reported | 0 |
| Race (NIH/OMB)(Participants) | Ipilimumab After Stem Cell Transplantation |
|---|---|
| American Indian or Alaska Native | 0 |
| Asian | 0 |
| Native Hawaiian or Other Pacific Islander | 0 |
| Black or African American | 0 |
| White | 3 |
| More than one race | 0 |
| Unknown or Not Reported | 0 |
| Region of Enrollment(Participants) | Ipilimumab After Stem Cell Transplantation |
|---|---|
| United States | 3 |
Documents are hosted by the registry — open the source record to download them.
Plan to share: Yes — Memorial Sloan Kettering Cancer Center supports the international committee of medical journal editors (ICMJE) and the ethical obligation of responsible sharing of data from clinical trials. The protocol summary, a statistical summary, and informed consent form will be made available on clinicaltrials.gov when required as a condition of Federal awards, other agreements supporting the research and/or as otherwise required. Requests for deidentified individual participant data can be made beginning 12 months after publication and for up to 36 months post publication. Deidentified individual participant data reported in the manuscript will be shared under the terms of a Data Use Agreement and may only be used for approved proposals. Requests may be made to: crdatashare@mskcc.org.
This study is terminated, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.
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