A Phase 1B, Open-Label Study of Elranatamab in Combination with Iberdomide in Participants with Relapsed Refractory Multiple Myeloma

The main purpose of the study is to understand how safe and tolerable is elranatamab when
given along with iberdomide.

There are 2 parts to this study. Part 1 will look at how safe and tolerable is
elranatamab when given with iberdomide. Part 2 will look at the correct amount of this
combination that can be given to patients with relapsed or refractory multiple myeloma.

Myeloma is a type of cancer that begins in plasma cells (white blood cells that produce
antibodies). Refractory means a disease or condition that does not respond to treatment.
Relapsed means the return of a disease after a period of improvement.

All study medicines are given in cycles that last 28 days. Everyone taking part in this
study will receive elranatamab as a shot under the skin. Iberdomide will be taken by
mouth once a day for 21 days over a 28-day cycle.

Participants will receive study medicine until:

- their disease progresses or,

- they experience unacceptable side effects or,

- they choose to no longer take part in the study.

The study will look at the experiences of people receiving the study medicines. This will
help see if the study medicines are safe and can be used for multiple myeloma treatment.

Inclusion Criteria:

- Prior diagnosis of multiple myeloma as defined by IMWG criteria

- Measurable disease based on IMWG criteria as defined by at least 1 of the following:

- Serum M-protein ≥0.5 g/dL by SPEP

- Urinary M-protein excretion ≥200 mg/24 hour by UPEP

- Serum immunoglobulin FLC ≥10 mg/dL (≥100 mg/L) AND abnormal serum immunoglobulin
kappa to lambda FL ratio (<0.26 or >1.65)

- Part 1: Received 2-4 prior lines of therapy for multiple myeloma, consisting of at
least 1 immunomodulatory drug and 1 proteasome inhibitor.

- Part 2: Received 1-3 prior lines of therapy for multiple myeloma, consisting of at
least 1 immunomodulatory drug and 1 proteasome inhibitor.

- ECOG performance status 0-1

- Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade ≤1

Exclusion Criteria:

- Plasma cell leukemia, Smoldering multiple myeloma, Waldenström's macroglobulinemia,
Amyloidosis, POEMS Syndrome

- Impaired cardiovascular function or clinically significant cardiovascular diseases

- Stem cell transplant within 12 weeks prior to enrollment or active graft vs host
disease

- Participants with any active, uncontrolled bacterial, fungal, or viral infection

- Any other active malignancy within 3 years prior to enrollment, except for
adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ

- Previous treatment with:

- BCMA-directed or CD3 redirecting therapy

- Iberdomide (CC-220) or Mezigdomide

- Administration of strong inhibitor or inducer of CYP3A4/5 within 2 weeks prior to
dosing and during the study

- Administration with an investigational product within 30 days preceding the first
dose of study intervention

- Participant is unable or unwilling to undergo protocol required thromboembolism
prophylaxis