Overview

Belantamab Mafodotin, Cyclophosphamide, and Dexamethasone in Relapsed/Refractory Multiple Myeloma

Status:
Not yet recruiting
Trial end date:
2024-03-01
Target enrollment:
0
Participant gender:
All
Summary
Evaluate the efficacy and safety of Belantamab Mafodotin, cyclophosphamide, and dexamethasone in patients with Relapsed/Refractory Multiple Myeloma
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Maryland, Baltimore
Treatments:
Cyclophosphamide
Dexamethasone
Criteria
Inclusion Criteria:

1. Histologically confirmed diagnosis of Refractory MM; failed at least 3 prior lines of
anti-myeloma treatments, including an anti-CD38 antibody (e.g., daratumumab) alone or
in combination, and is refractory to an IMiD (i.e., lenalidomide or pomalidomide), and
to a proteasome inhibitor (e.g., bortezomib, ixazomib or carfilzomib). (Refractory
myeloma is defined as disease that is nonresponsive while on primary or salvage
therapy or progresses within 60 days of last therapy. Nonresponsive disease is defined
as either failure to achieve at least minimal response or development of progressive
disease (PD) while on therapy).

2. Has measurable disease with at least one of the following:

1. Serum M-protein ≥0.5 g/dL (≥ 5 g/L)

2. Urine M-protein ≥ 200 mg/24h

3. Serum FLC assay: Involved FLC level ≥10 mg/dL and an abnormal ratio (<0.26 or
>1.65)

3. Provide signed written informed consent.

4. 18 years or older (at the time consent is obtained).

5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.

6. Participants with a history of autologous stem cell transplant or Prior BCMA targeted
therapy (e.g. CAR-T cells, BiTes) can enroll on the study provided that:

1. Therapy was >100 days prior to study enrolment.

2. No active infection(s).

7. Adequate organ system function (as defined by inclusion criteria #7).

8. Female and Male patients: Contraceptive use by men or women should be consistent with
local regulations regarding the methods of contraception for those participating in
clinical studies.

9. Prior treatment-related toxicities must be ≤ Grade 1 except peripheral neuropathy
(Grade-2).

Exclusion Criteria:

1. Systemic anti-myeloma therapy within ≤14 days or 5 half-lives, whichever is shorter,
or plasmapheresis within 7 days prior to treatment.

2. Systemic treatment with high dose steroids (equivalent to ≥ 60 mg prednisone daily for
≥4 days) within the past 14 days.

3. Symptomatic amyloidosis, active CNS disease, active plasma cell leukemia at the time
of screening.

4. Prior allogeneic stem cell transplant (SCT). NOTE - Participants who have undergone
syngeneic transplant may be allowed if no history of GvHD.

5. Current corneal epithelial disease except mild punctate keratopathy.

6. Evidence of active bleeding.

7. Any major surgery within the last four weeks.

8. Presence of active renal condition (infection, dialysis); isolated proteinuria from MM
is allowed provided participants fulfil the adequate organ system function criteria
(as defined by inclusion criteria #7).

9. Any serious and/or unstable pre-existing medical, psychiatric disorder or lab
abnormalities that affect patients' safety, obtaining informed consent or compliance
with study procedures.

10. Current unstable liver disease defined by the presence of ascites, encephalopathy,
coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice, or
cirrhosis. NOTE: Stable non-cirrhotic chronic liver disease (including Gilbert's
syndrome or asymptomatic gallstones) is acceptable if participant otherwise meets
entry criteria.

11. Other malignancies except for malignancy from which the patients have been
disease-free > 2 years.

12. Evidence of cardiovascular disease including any of the following:

1. Evidence of current clinically significant untreated arrhythmias, including
clinically significant ECG abnormalities including second degree (Mobitz Type II)
or third degree atrioventricular (AV) block.

2. History of myocardial infarction, acute coronary syndromes (including unstable
angina), coronary angioplasty, or stenting or bypass grafting within 3 months of
Screening.

3. Class III or IV heart failure as defined by the New York Heart Association
functional classification system.

4. Uncontrolled hypertension.

13. Known immediate or delayed hypersensitivity reaction or idiosyncratic reaction to
drugs chemically related to belantamab mafodotin, daratumumab, bortezomib, boron or
mannitol or any other components of the study treatment.

14. Active infection requiring treatment.

15. Known HIV infection.

16. Presence of hepatitis B surface antigen (HbsAg), or hepatitis B core antibody (HbcAb),
at screening or within 3 months prior to first dose of study treatment. Note: presence
of Hep B surface antibody (HBsAb) indicating previous vaccination will not exclude a
participant.

17. Positive hepatitis C antibody test result or positive hepatitis C RNA test result at
screening or within 3 months prior to first dose of study treatment.

NOTE: Participants with positive hepatitis C antibody due to prior resolved disease
can be enrolled, only if a confirmatory negative Hepatitis C RNA test is obtained.
Hepatitis RNA testing is optional and participants with negative hepatitis C antibody
test are not required to also undergo hepatitis C RNA testing.

18. Symptomatic amyloidosis, active POEMS syndrome (polyneuropathy, organomegaly,
endocrinopathy, monoclonal plasma proliferative disorder, skin changes) or active
plasma cell leukemia at the time of screening.

19. Pregnant or lactating female.

20. Concomitant administration of strong P-glycoprotein inhibitors and inhibitors of OATP
will be avoided.