OncoMatch

OncoMatch/Clinical Trials/NCT05199311

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

Is NCT05199311 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including Carfilzomib and Iberdomide for multiple myeloma.

Phase 1/2RecruitingHackensack Meridian HealthNCT05199311Data as of Jun 2026

Treatment: Carfilzomib · Iberdomide · Oral DexamethasoneThis is a multi-institution, open label, phase I/II study of Iberdomide, Carfilzomib, and dexamethasone (KID) in patients with newly diagnosed transplant eligible MM.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Targeted therapy

CarfilzomibIberdomide

Other

Oral Dexamethasone

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Max 1 prior line

Cannot have received: iberdomide (iberdomide)

Prior use of iberdomide

Cannot have received: systemic myeloma drug therapy

Exception: within the last 14 days of initiating IP

Use of any systemic myeloma drug therapy within the last 14 days of initiating IP

Cannot have received: investigational agent

Exception: within 28 days or 5 half-lives (whichever is longer) of initiating IP

Subject has been treated with an investigational agent (ie, an agent not commercially available) within 28 days or 5 half-lives (whichever is longer) of initiating IP

Lab requirements

Blood counts

ANC < 1,000/μL; Platelet count < 50,000/μL [excluded]

Kidney function

serious renal impairment (CrCl < 30 mL/min) or requiring dialysis [excluded]

Liver function

SGOT/AST or SGPT/ALT ≥ 2.5 x ULN; serum total bilirubin, direct bilirubin, or alkaline phosphatase ≥ 1.5 x ULN [excluded]

Cardiac function

LVEF < 40% by ECHO [excluded]; active congestive heart failure (NYHA III-IV), symptomatic ischemia, uncontrolled arrhythmias, QTc > 470 msec, pericardial disease, or MI within 4 months prior to randomization [excluded]

ANC < 1,000/μL; Platelet count < 50,000/μL; Corrected serum calcium > 13.5 mg/dL; SGOT/AST or SGPT/ALT ≥ 2.5 x ULN; serum total bilirubin, direct bilirubin, or alkaline phosphatase ≥ 1.5 x ULN; CrCl < 30 mL/min or requiring dialysis; LVEF < 40% by ECHO

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

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

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05199311 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior iberdomide, systemic myeloma drug therapy, investigational agent disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify