Pembrolizumab, Ixazomib Citrate, and Dexamethasone in Treating Participants With Relapsed Multiple Myeloma

PRIMARY OBJECTIVES:

I. To determine the overall response rate (>= partial response [PR]) of pembrolizumab in
combination with standard doses of ixazomib citrate (ixazomib) and dexamethasone, in patients
with relapsed symptomatic multiple myeloma (MM).

SECONDARY OBJECTIVES:

I. To determine the ? very good partial response (VGPR) and complete response (CR) rate of
pembrolizumab added to standard doses of ixazomib and dexamethasone in relapsed myeloma.

II. To determine the progression free survival and overall survival among patients with
relapsed MM following treatment with the combination of pembrolizumab, ixazomib and
dexamethasone.

III. To determine the toxicities associated with pembrolizumab added to standard doses of
ixazomib and dexamethasone in patients with relapsed MM.

CORRELATIVE RESEARCH:

I. PDL-1 expression on myeloma cells and non-tumor cell compartments from the bone marrow
will be assessed at baseline.

II. Measures of T-cell activation / exhaustion will be assessed at baseline and after cycle 1
and cycle 3.

III. Natural killer (NK) cell function and numbers will be evaluated at baseline and after
cycle 1 and cycle 3.

OUTLINE:

Participants receive ixazomib citrate orally (PO) on days 1, 8, 15, 29, 36, 43, 57, 64, and
71 and pembrolizumab intravenously (IV) over 30 minutes on days 1, 22, 43, 64. Participants
also receive dexamethasone PO on days 1, 8, 15, 29, 36, 43, 57, 64, and 71. Courses with
dexamethasone repeat every 84 days for up to 1 year and courses with ixazomib citrate and
pembrolizumab repeat every 84 days for up to 2 years in the absence of disease progression or
unacceptable toxicity.

After completion of study treatment, patients are followed up every 3 months until
progressive disease, and then every 6 months for up to 2 years.

Inclusion Criteria:

- Diagnosis of relapsed, symptomatic multiple myeloma by International Myeloma Working
Group (IMWG) diagnostic criteria for multiple myeloma

- Obtained ? 14 days prior to registration: Calculated creatinine clearance (using
Cockcroft-Gault equation below) ? 30 mL/min

- Obtained ? 14 days prior to registration: Absolute neutrophil count (ANC) ? 1000/mm^3

- Obtained ? 14 days prior to registration: Platelet count ? 75000/mm^3; Note: Platelet
transfusion is not allowed ? 3 days prior to registration

- Obtained ? 14 days prior to registration: Hemoglobin ? 8.0 g/dL

- Obtained ? 14 days prior to registration: Total bilirubin ? 1.5 x upper limit of
normal (ULN)

- Obtained ? 14 days prior to registration: Alanine aminotransferase (ALT) and aspartate
aminotransferase (AST) ? 2.5 x ULN

- Must have relapsed or refractory disease after treatments including three therapies:
proteasome inhibitors, immunomodulatory imide drugs (IMiDs), and anti-CD38 antibody

- Measurable disease of multiple myeloma as defined by at least ONE of the following:

- Serum monoclonal protein ? 1.0 g/dL

- ? 200 mg of monoclonal protein in the urine on 24 hour electrophoresis

- Serum immunoglobulin free light chain ? 10 mg/dL AND abnormal serum
immunoglobulin kappa to lambda free light chain ratio

- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, or 1

- Provide informed written consent

- Negative pregnancy test done ? 7 days prior to registration, for women of childbearing
potential only

- Willing to follow strict birth control measures;

- Female patients: If they are of childbearing potential, agree to one of the
following:

- Practice 2 effective methods of contraception, at the same time, from the
time of signing the informed consent form through 120 days after the last
dose of study drug, AND must also adhere to the guidelines of any
treatment-specific pregnancy prevention program, if applicable, OR

- Agree to practice true abstinence when this is in line with the preferred
and usual lifestyle of the subject; (periodic abstinence [eg, calendar,
ovulation, symptothermal, post-ovulation methods] and withdrawal are not
acceptable methods of contraception)

- Male patients: even if surgically sterilized (i.e., status post-vasectomy), must
agree to one of the following:

- Agree to practice effective barrier contraception during the entire study
treatment period and through 120 days after the last dose of study drug, OR

- Must also adhere to the guidelines of any treatment-specific pregnancy
prevention program, if applicable, OR

- Agree to practice true abstinence when this is in line with the preferred
and usual lifestyle of the subject; (periodic abstinence (eg, calendar,
ovulation, symptothermal, post-ovulation methods] and withdrawal are not
acceptable methods of contraception)

- Willing to return to enrolling institution for follow-up (during the Active Monitoring
Phase of the study)

- Willing to provide bone marrow and blood samples for planned research

Exclusion Criteria:

- Myeloma disease that is refractory to ixazomib treatment

- Has a known additional malignancy that is progressing or requires active treatment;
exceptions include early stage cancers (carcinoma in situ or stage 1) treated with
curative intent, basal cell carcinoma of the skin, squamous cell carcinoma of the
skin, in situ cervical cancer, or in situ breast cancer that has undergone potentially
curative therapy

- Any of the following:

- Pregnant women

- Nursing women

- Men or women of childbearing potential who are unwilling to employ adequate
contraception

- Other co-morbidity which would interfere with patient's ability to participate in
trial, e.g. uncontrolled infection, uncompensated heart or lung disease

- Other concurrent chemotherapy, or any ancillary therapy considered investigational ?
14 days prior to study registration; NOTE: Bisphosphonates are considered to be
supportive care rather than therapy, and are thus allowed while on protocol treatment

- Peripheral neuropathy ? grade 3 on clinical examination or grade 2 with pain during
the screening period

- Major surgery ? 14 days prior to study registration

- Radiotherapy ? 14 days prior to registration; NOTE: If the involved field is small, 7
days will be considered a sufficient interval between treatment and administration of
study drugs

- Participation in any other clinical trials with other investigational agents not
included in this trial ? 21 days prior to registration

- Has active autoimmune disease that has required systemic treatment ? 2 years prior to
study registration (i.e. with use of disease modifying agents, corticosteroids or
immunosuppressive drugs);

- NOTE: Replacement therapy (e.g., thyroxine, insulin, or physiologic
corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.)
is not considered a form of systemic treatment

- Has a history of (non-infectious) pneumonitis that required steroids or current
pneumonitis

- Has a known history of interstitial lung disease

- Has an active infection requiring systemic therapy

- Has a history of current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the trial, interfere with the subject?s
participation for the full duration of the trial, or is not in the best interest of
the subject to participate, in the opinion of the treating investigator

- Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial

- Is pregnant or breastfeeding, or expecting to conceive or father children within the
projected duration of the trial, starting with the pre-screening or screening visit
through 120 days after the last dose of trial treatment

- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent

- Has a known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies)

- Has known active hepatitis B (e.g., hepatitis B surface antigen [HBsAg] reactive) or
hepatitis C (e.g., hepatitis C virus [HCV] ribonucleic acid [RNA] [qualitative] is
detected)

- Has a known history of active TB (Bacillus tuberculosis)

- Has received a live vaccine ? 30 days prior to study registration

- Has known active central nervous system (CNS) metastases and/or carcinomatous
meningitis

- Allogeneic hematopoietic stem cell transplant

- Systemic treatment with strong CYP3A inducers (rifampin, rifapentine, rifabutin,
carbamazepine, phenytoin, phenobarbital), or use of St. John?s wort ? 14 days prior to
registration

- Known gastrointestinal (GI) disease or GI procedure that could interfere with the oral
absorption or tolerance of ixazomib including difficulty swallowing