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Iberdomide (CC-220) Priming to Improve T Cell Fitness Prior to Leukapheresis for Chimeric Antigen Receptor T Cell (CAR-T) Therapy for Relapsed/Refractory Multiple Myeloma (RRMM)

22. Juli 2026 aktualisiert von: Shambavi Richard

Feasibility Study of Iberdomide (CC-220) Priming to Improve T Cell Fitness Prior to Leukapheresis for Chimeric Antigen Receptor T Cell (CAR-T) Therapy for Relapsed/Refractory Multiple Myeloma (RRMM)

This feasibility trial studies the efficacy of administering iberdomide (CC-220) as a priming agent prior to leukapheresis in patients with relapsed/refractory multiple myeloma (RRMM) who are already planned for standard-of-care CAR-T therapy. Giving iberdomide before CAR-T may improve T cell fitness which may improve CAR-T expansion kinetics and response after infusion.

Studienübersicht

Detaillierte Beschreibung

In this feasibility study, patients with RRMM planned for standard of care CAR-T will be approached for consent for enrollment. Participating patients will receive one 28-day cycle of iberdomide at a dose of 1.0 mg daily, using a dosing schedule of 1.0 mg once daily for 21 days followed by 7 days off. After completion of the 28-day cycle, patients will proceed with leukapheresis on day 29 of therapy, with allowance for up to a 14-day delay in leukapheresis if needed. Blood samples will be collected on day 1 (prior to iberdomide exposure) and on the day of leukapheresis to compare T cell profiling before and after iberdomide priming. After leukapheresis, patients will proceed with standard of care management, including bridging therapy if indicated, until CAR-T infusion. After infusion, blood samples will be collected daily during initial hospitalization, then weekly for 1 month, and then monthly for up to 1 year. Blood samples will be evaluated for maximal CAR-T and ALC expansion and CAR-T persistence. Patients will be monitored per standard of care protocols for clinical efficacy and toxicity after CAR-T therapy for up to 1 year.

Studientyp

Interventionell

Einschreibung (Geschätzt)

22

Phase

  • Frühphase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

    • New York
      • New York, New York, Vereinigte Staaten, 10029
        • Icahn School of Medicine at Mount Sinai
        • Kontakt:
        • Kontakt:
        • Hauptermittler:
          • Shambavi Richard

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

INCLUSION CRITERIA

  • 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.
  • All subjects must have documented diagnosis of MM and be eligible for commercial CAR-T therapy with either cilta-cel or ide-cel.
  • All subjects must have ≥2 prior lines of multiple myeloma directed therapy, as determined by their treating clinician
  • All patients must have ECOG Performance Status ≤ 2.
  • Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy tests (minimum sensitivity 25 IU/L or equivalent units of hCG), at screening (10-14 days prior to start of study drug); another within 24 hours prior to the start of study drug.
  • Women must not be breastfeeding
  • WOCBP must agree to follow instructions for method(s) of contraception for 1 month (4 weeks) before the start of treatment with study drugs, for the duration of treatment with study drugs, and for a total of 1 month (4 weeks) after completion of iberdomide.
  • Males who are sexually active with WOCBP must always use a latex or synthetic condom during any sexual contact with females of reproductive potential while taking Iberdomide (CC-220) and for up to 90 days after discontinuing Iberdomide (CC-220), even if they have undergone a successful vasectomy. Male patients must not donate sperm.
  • Azoospermic males and WOCBP who are continuously not heterosexually active are exempt from contraceptive requirements. However, they must still undergo pregnancy testing as described in this section.
  • All subjects must agree not to share study medication.

EXCLUSION CRITERIA

  • Subjects with monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), primary amyloidosis (no active multiple myeloma), Waldenström's macroglobulinemia, or POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes)
  • Subjects with active plasma cell leukemia (defined as either 20% of peripheral blood white blood cell count comprised of plasma/CD138+ cells or an absolute plasma cell count of 2 x 109/L)
  • Subjects with active Central Nervous System involvement with multiple myeloma
  • Subjects with active multiple myeloma that cannot be safely managed with single-agent iberdomide for the duration of the priming period, per the discretion of the treating physician or PI
  • Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from signing the informed consent form
  • Any serious concurrent medical conditions that may make the patient non-evaluable or put the patient's safety at risk, per the discretion of the treating physician or PI
  • Subjects with an active infection that requires parenteral anti-infective treatment within 7 days
  • Unable to tolerate thromboembolic prophylaxis while on iberdomide
  • Severe hypersensitivity reaction to prior IMiD (thalidomide, lenalidomide or pomalidomide)
  • Grade > 2 peripheral neuropathy (per NCI CTCAE v5.0)
  • Patients with a positive PCR test for hepatitis B virus or hepatitis C virus indicating active infection. Patients with positive serologic testing indicating exposure will need confirmatory testing by PCR.
  • Patients with detectable HIV viral load or known acquired immunodeficiency syndrome (AIDS).
  • Prior or concurrent malignancy, except for the following:

    • Adequately treated basal cell or squamous cell skin cancer or in-situ carcinoma.
    • Non-muscle invasive bladder cancer treated within the last 24 months that is considered completely cured.
    • Localized prostate cancer (N0M0):
    • with a Gleason score of ≤6, treated within the last 24 months or untreated and under surveillance,
    • with a Gleason score of 3+4 that has been treated more than 6 months prior to full study screening and considered to have a very low risk of recurrence; or
    • any history of localized prostate cancer and receiving androgen deprivation therapy and considered to have a very low risk of recurrence per the discretion of the treating physician or PI
    • Non-invasive cervical cancer treated within the last 24 months that is considered completely cured.
    • Breast cancer: adequately treated lobular carcinoma in situ, or ductal carcinoma in situ, or history of localized breast cancer and receiving anti-hormonal agents and considered to have a very low risk of recurrence.
    • Any other cancer from which the subject has been disease free for > 3 years prior to study entry, or considered cured with minimal risk of disease recurrence.
  • Prior treatment with Iberdomide (CC-220) within 6 months prior to enrollment
  • Prior allogeneic stem cell transplant except subjects who have completed the stem cell transplant > 12 months prior to first dose of study drug, have no history of graft versus host disease, and are not on systemic immunosuppressive therapy
  • Major cardiac surgery within 8 weeks prior to the first dose of study drug; all other major surgery within 4 weeks prior to the first dose of study drug.
  • Subjects with following physical and laboratory test findings:

    • Absolute neutrophil count < 1 x 109/L without growth factor support within 1 week, or absolute neutrophil count < 0.5 x 109/L for patients with documented Duffy-null blood typing
    • Platelets < 50 x 109/L without transfusion support within 1 week
    • Creatinine clearance < 30 ml/min according to the Cockroft-Gault formula:
  • Female CrCl = [(140 - age in years) x weight in kg x 0.85] / [72 x serum creatinine in mg/dl]
  • Male CrCl = [(140 - age in years) x weight in kg x 1.00] / [72 x serum creatinine in mg/dl]

    • Total bilirubin ≥ 2 x ULN (≥ 3 x ULN if documented Gilbert's syndrome)
    • AST or ALT ≥ 3x ULN
    • Corrected serum calcium > 13.5 mg/dL
  • Are also excluded:

    • Prisoners or subjects who are involuntarily incarcerated
    • Subjects who are compulsorily detained for treatment of either a psychiatric or physical (e.g., infectious disease) illness

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Patients with RRMM
Patients with RRMM who are already planned for standard-of-care CAR-T therapy. Study participants will be planned for one cycle (28 days) of iberdomide therapy (1.0mg daily on days 1-21 of a 28-day cycle), followed by CAR-T leukapheresis. Patients will then proceed with CAR-T infusion per standard of care, with additional lab monitoring for T cell phenotyping and CAR-T expansion kinetics.
1.0mg iberdomide capsules administered orally, daily on days 1-21 of a 28-day cycle
Andere Namen:
  • CC-220
A procedure in which blood is collected and white blood cells (including T cells) are separated and collected. The remaining blood components are returned to the participant. The collected T cells will be used to manufacture the CAR-T cell therapy.
Participants will receive an intravenous infusion of standard-of-care CAR-T therapy manufactured from the participant's previously collected cells

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Proportion of patients with T cell effector memory (TEM) expansion following iberdomide priming.
Zeitfenster: On the day of leukapheresis, after completing iberdomide therapy on Day 29
Proportion of patients with T cell effector memory (TEM) expansion following iberdomide priming, defined as an absolute increase of >10 percentage points or a relative increase of >50% in TEM cells.
On the day of leukapheresis, after completing iberdomide therapy on Day 29

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in Proportion of T cell subsets from baseline after iberdomide priming
Zeitfenster: On the day of leukapheresis, after completing iberdomide therapy on Day 29
Proportion of T cell subsets (including terminally differentiated effector, exhausted, and activated T cells) present for each participant in the feasibility evaluable (FE) population at leukapheresis (Priming D29 after iberdomide) to baseline (Priming-D1).
On the day of leukapheresis, after completing iberdomide therapy on Day 29
Cmax with iberdomide priming prior to leukapheresis
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Cmax is the highest measured concentration of iberdomide. Cmax will be assessed in the CAR-T evaluable (CARTE) population
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Tmax with iberdomide priming prior to leukapheresis,
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Time to reach Cmax. Tmax will be assessed in CAR-T (CARTE) population
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
AUC0-14 with iberdomide priming prior to leukapheresis
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Total Exposure over time. AUC0-14 will be assessed in the CAR-T evaluable (CARTE) population.
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
CAR-T persistence with iberdomide priming prior to leukapheresis,
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
CAR-T persistence will track therapy effectiveness over time. CAR-T persistence will be assessed in the CAR-T evaluable (CARTE) population.
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
ALCmax with iberdomide priming prior to leukapheresis
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Absolute Lymphocyte Count (ALC) is a key blood test measuring the exact number of lymphocytes. ALCmax measures the maximum count overtime. ALCmax will be assessed in the CAR-T evaluable (CARTE) population.
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Time to ALCmax with iberdomide priming prior to leukapheresis
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Time to reach absolute lymphocyte count maximum (ALCmax) in the CAR-T evaluable (CARTE) population.
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Absolute lymphocyte count (ALC) expansion kinetics as a proxy for CAR-T expansion
Zeitfenster: After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
After CAR-T infusion at Day 14, Day 28, Month 3, Month 6, Month 12
Overall response rate
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12
Overall response rate (ORR), defined as the proportion of patients that achieve at least a partial response according to IMWG criteria
After CAR-T at Day 100 (~Month 3) and Month 12
Measurable residual disease
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Rate of measurable residual disease (MRD)-negativity and MRD-negative complete response (CR) as defined by IMWG response criteria
After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Progression-free survival
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Progression-free survival (PFS), defined as the time from CAR-T infusion until progression by IMWG response criteria or death
After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Overall survival
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Overall survival (OS), defined as the time from CAR-T infusion until death
After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Duration of response
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Duration of response (DOR), defined as time from first observed response after CAR-T until progression by IMWG criteria
After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Time to next treatment
Zeitfenster: After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.
Time to next treatment (TTNT), defined as the time from CAR-T infusion until initiation of the next line of myeloma-directed therapy for subsequent relapsed disease
After CAR-T at Day 100 (~Month 3) and Month 12. Long-term follow-up for up to 5 years.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Mitarbeiter

Ermittler

  • Hauptermittler: Shambavi Richard, MD, Icahn School of Medicine at Mount Sinai

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juli 2026

Primärer Abschluss (Geschätzt)

1. Juli 2027

Studienabschluss (Geschätzt)

1. Juli 2031

Studienanmeldedaten

Zuerst eingereicht

16. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

22. Juli 2026

Zuerst gepostet (Tatsächlich)

27. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

27. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

22. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

The completed dataset is the sole property of the Sponsor-Investigator's institution and should not be exported to third parties, except for authorized representatives of appropriate Health/Regulatory Authorities, without permission from the Sponsor-investigator and their institution.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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