Carfilzomib, Iberdomide (CC-220) and Dexamethasone (KID) in Transplant Eligible Multiple Myeloma

Paused · Phase 1/Phase 2

Conditions studied: Multiple Myeloma

In brief

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.

Key facts

Study ID

NCT05199311

Run by

Hackensack Meridian Health

People needed

66

Starts

2022-05-13

Expected to finish

2027-03-01

Last updated by the study team

2026-07-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Documented newly diagnosed multiple myeloma
• a. At least 25% of patients accrued should be high risk as defined by IMWG or mSMART criteria.
• Patient should be deemed transplant eligible.
• Patients may not have had more than 1 cycle of prior induction therapy. If a patient has had 1 cycle of prior multiple myeloma therapy, the patient must have had documented measurable disease prior to initiation of cycle 1.
• Subjects must satisfy the following criteria to be enrolled in the study:
• Subject is ≥ 18 years of age at the time of signing the informed consent form (ICF).
• Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted.
• Subject is willing and able to adhere to the study visit schedule and other protocol requirements.
• Subjects must have a documented diagnosis of MM and have measurable disease defined as:
• M-protein (serum and/or urine protein electrophoresis (sPEP or uPEP)): sPEP≥0.5 g/dL or uPEP ≥ 200 mg/24 hours and/or
• Light chain MM without measurable disease in the serum or urine: serum immunoglobulin free light chain ≥ 10 mg/dL (100 mg/L) and abnormal serum immunoglobulin kappa lambda free light chain ratio
• Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2.
• A female of childbearing potential (FCBP) is a female who: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral salpingectomy, or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (ie, has had menses at any time in the preceding 24 consecutive months) and must:
• a. Have two negative pregnancy tests as verified by the Investigator prior to starting study treatment. She must agree to ongoing pregnancy testing during the course of the study, and after end of study treatment. This applies even if the subject practices true abstinence from heterosexual contact.
• Either commit to true abstinence from heterosexual contact (which must be reviewed on a monthly basis and source documented) or agree to use, and be able to comply with two forms of contraception: one highly effective, and one additional effective (barrier) measure of contraception without interruption 28 days prior to starting investigational product, during the study treatment (including dose interruptions), and for at least 28 days after the last dose of iberdomide.
• Male subjects must:
• a. Male subjects must practice complete abstinence (True abstinence is acceptable when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence [e.g. calendar, ovulation, symptothermal or post-ovulation methods] and withdrawal are not acceptable methods of contraception.) or agree to use a condom during sexual contact with a pregnant female or a FCBP while taking iberdomide, during dose interruptions and for at least 28 days following the last dose of iberdomide even he has undergone a successful vasectomy.
• Males must agree to refrain from donating sperm while on study treatment, during dose interruptions and for at least 28 days following last dose of study treatment.
• All subjects must agree to refrain from donating blood while on study treatment, during dose interruptions and for at least 28 days following the last dose of study treatment.
• All male and female subjects must follow all requirements defined in the Pregnancy Prevention Program.
• Note: A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient.

You may not qualify if…

• Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study
• Subject has any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study
• Subject has any condition that confounds the ability to interpret data from the study
• Subject has nonsecretory multiple myeloma
• Subjects with Plasma Cell leukemia or amyloidosis (with the exception of isolated marrow involvement).
• Any of the following laboratory abnormalities:
• Absolute neutrophil count (ANC) < 1,000/μL
• Platelet count < 50,000/μL. It is not permissible to transfuse subjects to achieve minimum platelet counts.
• Corrected serum calcium > 13.5 mg/dL (> 3.4 mmol/L)
• Serum glutamic oxaloacetic transaminase (SGOT)/aspartate aminotransferase (AST) or serum glutamic pyruvic transaminase (SGPT)/alanine aminotransferase (ALT) ≥ 2.5 x upper limit of normal (ULN)
• Serum total bilirubin, direct bilirubin, or alkaline phosphatase ≥ 1.5 x ULN
• Subjects with serious renal impairment ([CrCl] < 30 mL/min) or requiring dialysis would be excluded
• Subjects with peripheral neuropathy ≥ Grade 2
• Subjects with gastrointestinal disease that may significantly alter the absorption of iberdomide
• Subjects with a prior history of malignancies, other than MM, unless the subject has been free of the disease for ≥ 3 years with the exception of the following noninvasive malignancies:
• Basal cell carcinoma of the skin
• Squamous cell carcinoma of the skin
• Carcinoma in situ of the cervix
• Carcinoma in situ of the breast
• Incidental histological findings of prostate cancer such as T1a or T1b using the Tumor/Node/Metastasis (TNM) classification of malignant tumors or prostate cancer that is curative
• Subject has a history of anaphylaxis or hypersensitivity to thalidomide, lenalidomide, or pomalidomide
• Contraindications to the other treatment regimens, as per local prescribing information
• Subject has received any of the following within the last 14 days of initiating IP:
• Plasmapheresis
• Major surgery (as defined by the Investigator)

Where it is running

• Lombardi Comprehensive Cancer Center — Washington D.C., District of Columbia, United States
• John Theurer Cancer Center — Hackensack, New Jersey, United States

Full record on ClinicalTrials.gov

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