This is a multi-institution, open label, phase I/II study of Iberdomide, Carfilzomib, and dexamethasone (KID) in patients with newly diagnosed transplant eligible multiple myeloma
This trial has suspended patient recruitment.
This is a multi-institution, open label, phase I/II study of Iberdomide, Carfilzomib, and dexamethasone (KID) in patients with newly diagnosed transplant eligible MM.
As part of a dose escalation phase, the first 10 patients will be enrolled at dose level -1 (Iberdomide 1.1 mg po daily days 1-21). Two months after the first 10 patients have completed at least 2 cycles of therapy in dose level -1, an Independent Safety Review Committee will review the safety data. Assuming the combination is determined to have adequate safety and tolerability, 10 patients will be enrolled at dose level 1 (Iberdomide 1.3 mg po daily days 1-21). After an independent safety review two months after 10 patients have completed at least 2 cycles of therapy in dose level 1, the remaining 46 patients will be enrolled at dose level 2 (Iberdomide 1.6 mg po daily days 1-21).
Treatment will continue for up to 4 cycles (28 days) at the physician's discretion followed by the Autologous Stem Cell Transplant. Patients will be followed every 3 months for up to 2 years, or until disease progression or the start of a new line of therapy.
The following criteria is a partial list of reasons why patients may be eligible to participate in this clinical trial. Further evaluation with a medical professional is required.
Inclusion Criteria:
Exclusion Criteria:
Phase 1/2
Enrollment: 66 patients (estimated)
View MoreSeptember 26, 2026
Investigators from multiple cancer centers studied how patients with newly diagnosed multiple myeloma (NDMM) would tolerate a combination of carfilzomib, iberdomide (iber), and dexamethasone (KID) prior to receiving autologous stem cell transplantation (ASCT).
Fifty-eight patients were enrolled in the KID clinical trial, which entailed receiving the combination treatment for two to three 28-day cycles followed by ASCT. The main goal was to see at least half of the patients, if not more, achieve stringent complete response (sCR) or complete response (CR). The investigators prescribed doses of 1mg, 1.3 mg, or 1.6 mg to patients with NDMM.
The 58 patients completed a median of three cycles and had a median treatment duration of 85 days.
Investigators followed up patients in the trial at 13.3 months. At interim analysis, best ORR was 98%, sCR/CR was 31%, very good partial response (VGPR) was 21%, and partial response (PR) rates were 47%.
Half of patients experienced adverse events (AEs): 22% had anemia, 14% had neutropenia, 9% had thrombocytopenia, and 36% had infections (all grade 1/2). Serious AEs occurred in 12 patients, including atrial fibrillation (AFib) and erythema multiforme, which presents with distinctive bullseye-shaped skin rashes.
Overall survival (OS) at 6, 12, and 24 months was 98%, 98.1%, and 95%, and 100%, 100%, and 93% for the high-risk group, respectively. The progression-free survival (PFS) rates at 6, 12, and 24 months were 96%, 94%, and 90% overall and 100%, 94%, and 86% for the high-risk subset.
Noa Biran, MD, Associate Professor at the Hackensack Meridian Health John Theurer Cancer Center, presented these results at the 23rd International Myeloma Society (IMS) Annual Meeting in Glasgow, Scotland, in late September.
The research team concluded that 31% of patients who received the KID triplet therapy following ASTC overall and 31% in the high-risk NDMM groups at interim analysis, signaling progress in this difficult-to-treat disease. They write that future studies will evaluate KID with post-AST iber plas elranatamab followed by iber maintenance.
December 09, 2023
At data cutoff (July 14, 2023), there were 13 patients enrolled, which included 11 and 2 patients enrolled in the phase 1 and 2 studies, respectively. Ten patients are on trial, 2 were screen failures, and 1 is in screening. Of the 10 patients on trial, the median age was 66 years (range 46-78), 40% male, 70% white, and 30% had ISS stage II MM. Four unique patients had high-risk cytogenetics, which included 2 patients with t(4;14), 2 with 1q21 duplication, 1 with t(14;16), 1 with del(17p)/monosomy 17, and 1 with TP53 mutation.
In the phase 1 study, 3 patients enrolled at the starting dose level of iberdomide 1 mg. Grade 1-2 TEAEs occurred in all 3 patients, but no DLTs occurred. The next 3 patients were enrolled at the iberdomide dose of 1.3 mg. Grade 1-2 TEAEs occurred in 2 patients (rash and pruritus), but no grade ≥3 TEAEs were observed. Three patients were enrolled into the final dose level of iberdomide 1.6 mg. Grade 1-2 TEAEs occurred in 2 patients, and 2 patients experienced grade 3 TEAEs (rash and neutropenia). As no DLTs occurred, the MTD of iberdomide was determined to be 1.6 mg given in combination with CFZ and DEX.
Patients on trial (n=10; 6 in follow-up and 4 actively receiving treatment) have completed a median of 3 (range 2-4) cycles of KID. Of these patients, 7/10 experienced TEAEs (Table 1). No treatment-related deaths occurred. The most common TEAEs were maculopapular rash (46%), elevated liver function tests (38%), gastrointestinal symptoms (31%), and neutropenia (23%). Grade 3 TEAEs occurred in 2 patients (rash and neutropenia). One patient experienced a SAE of erythema multiforme on two separate occurrences (grade 1 and grade 2), which resolved with drug interruption. In 9 patients with response data available, the best ORR was 100% (CR, 1 [12%]; very good partial response [VGPR], 4 [44%]; partial response [PR], 4 [44%]). Six patients proceeded to ASCT with a median amount of stem cells mobilized of 9.42 x 106 cells/kg (range 4.84-13.53). At 3-months post-ASCT, the ORR was 100% (CR, 3 [50%]; VGPR, 2 [33%]; PR, 1 [17%]). One patient had documented sCR and MRD-negativity at data cutoff. Median PFS was not reached (NR) (95% CI, NR-NR).
View all clinical trial locations sorted by state.
Hackensack, NJ
Washington, DC
We know how difficult and confusing this process can be. If you are interested in this clinical trial or have questions, you can call us at any time. You can also send us a direct message with questions.
(888) 828-2206If you are interested in keeping an eye on this trial, you can add it to your list of favorite trials. We'll send you alerts when this trial is updated.
You can explore trial locations from around the US and connect directly with a trial coordinator.
Find Nearby LocationsYou can print an overview of this trial to take in to your next appointment. Your doctor can help you understand if this trial may be right for you.
Still need help? Send us a message