A Trial for Relapsed Multiple Myeloma Patients (Isatuximab-dexamethasone)

NCT ID: NCT04965155

Last Updated: 2025-02-25

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-21
• Study Completion Date: 2027-03-31

Brief Summary

This is an open label phase II study designed to assess the efficacy and safety of the combination isatuximab-dexamethasone pre and post transplant in relapsed MM patients. Before enrolment, patients have already received a reinduction therapy, as per local protocols, in order to achieve an optimal cytoreduction. Since carfilzomib-based regimens (eg. carfilzomib-lenalidomide-dexamethasone or carfilzomib-dexamethasone) are the current standard in Italy, for uniformity the use of one of these combinations is recommended. However, any cytoreductive treatment, excluding anti-CD38 antibodies containing regimens, as per local practice, is acceptable. During this period, if necessary, it will be possible to mobilize and collect peripheral blood stem cells. After the pre-enrollment cytoreduction period (reinduction therapy), patients have achieved at least a PR according to IMWG Response criteria.

After study enrolment, patients will receive 3 courses of isatuximab in combination with dexamethasone; after cycle 3 patients will receive ASCT, that will be conditioned with melphalan and will be followed by reinfusion of cryopreserved autologous stem cells. At 2 months after ASCT, patients will start maintenance, consisting in the administration of isatuximab in combination with dexamethasone for 12 cycles. Starting from cycle 13 onwards, only isatuximab will be administered until progression or intolerance.

Conditions

Relapsed Multiple Myeloma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Isatuximab-Dexamethasone

Isatuximab-Dexamethasone pre and post transplant in relapsed multiple myeloma patients.

Group Type: EXPERIMENTAL

Isatuximab-dexamethasone

Intervention Type: DRUG

Isatuximab 10 mg/kg IV: 1,8,15 and 22 at cycle 1; days 1 and 15 at cycles 2-3 Dexamethasone 40 mg OS: 1,8,15 and 22 at cycle 1; days 1 and 15 at cycles 2-3

Interventions

Isatuximab-dexamethasone

Isatuximab 10 mg/kg IV: 1,8,15 and 22 at cycle 1; days 1 and 15 at cycles 2-3 Dexamethasone 40 mg OS: 1,8,15 and 22 at cycle 1; days 1 and 15 at cycles 2-3

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patient has given voluntary written informed consent

2. Patient is willing and able to comply with the study visits and procedures required per protocol

3. Subject must have at least 18 and = 70 years of age

4. Patient has a life-expectancy = 3 months

5. Subject has received an ASCT in the first line of therapy with a progression/relapse after at least 24 months

6. Subject must have received any cytoreductive treatment, excluding anti-CD38 antibodies containing regimens, as per local practice for the first relapse, according to local guidelines. Carfilzomib-based combinations are recommended (eg. carfilzomib-lenalidomidedexamethasone or carfilzomib-dexamethasone). After the salvage duration phase (reinduction therapy), subject has achieved at least a PR according to IMWG Response criteria.

7. Subject must have documented relapsed MM as per IMWG criteria, and achieved at least a partial remission with treatments as per local guidelines

8. Subject must have at least 2.0 x 106 CD34+/Kg cryopreserved autologous stem cells

9. Subject must have an ECOG Performance Status score of 0, 1

10. Subject must have the following laboratory values:

• Platelet count =50 x 109/L (=30 x 109 /L if myeloma involvement in the bone marrow is > 50%) within 14 days prior to drug administration)
• Absolute neutrophil count (ANC) = 1 x 109/L without the use of growth factors
• Corrected serum calcium =14 mg/dL (3.5 mmol/L)
• Alanine transaminase (ALT): = 3 x the ULN
• Total bilirubin: = 2 x the ULN
• Calculated or measured creatinine clearance: = 30 mL/minute

11. Female subjects are eligible to participate if they are not pregnant, not breastfeeding, and at least one of the following conditions applies:

• they are not females of childbearing potential (FCBP), OR
• they are FCBP who have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10 - 14 days prior to and again within 24 hours of starting study medication and before each cycle of study treatment and must either commit to continue abstinence from heterosexual intercourse or apply a highly effective method of birth control during the intervention period and for at least 5 months after the last dose of study treatment. Of note: contraception duration should take also into consideration any backbone therapy

12. Male subjects must agree to use contraception on this protocol during the intervention period and for at least 5 months after the last dose of study treatment and refrain from donating sperm during this period

Exclusion Criteria

1. Previous therapy with daratumumab, isatuximab or any other anti-CD38 monoclonal antibody

2. MM localization to the central nervous system

3. Subjects who have received any investigational drug within 14 days or 5 half-lives of the investigational drug from eligibility confirmation, whichever is longer

4. Subjects who have received an allogeneic stem cell transplant

5. Subject with a history of malignancy (other than multiple myeloma) within 3 years before the date of eligibility confirmation (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or malignancy that in the opinion of the investigator, in agreement with the medical monitor, is considered cured with minimal risk of recurrence within 3 years)

6. Subject is known to be seropositive for human immunodeficiency virus (HIV) or with an active hepatitis A, B and C infection, defined as a positive test for hepatitis B surface antigen [HBsAg] and a positivity for HAV-RNA, HBV-DNA or HCV-RNA

7. Subject with any concurrent, clinically significant, uncontrolled medical condition or disease (eg, active systemic infection) that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study

8. Subject with active tuberculosis and severe infections requiring treatment with an antibiotic parenteral administration

9. Subject with hypersensitivity or history of intolerance to steroids, mannitol, pregelatinized starch, sodium stearyl fumarate, histidine (as base and hydrochloride salt), arginine hydrochloride, poloxamer 188, sucrose or any of the other components of study therapy that are not amenable to premedication with steroids and H2 blockers or would prohibit further treatment with these agents

10. Subject with pulmonary deficit, defined as FEV1 <65% and/or DLCO <65%

11. Subject with clinically significant cardiac disease, including:

• LVEF <50%
• Myocardial infarction within 6 months before eligibility confirmation, or unstable or
• Uncontrolled disease/condition related to or affecting cardiac function (eg, unstable angina, congestive heart failure, New York Heart Association Class III-IV)
• Cardiac arrhythmia (Common Terminology Criteria for Adverse Events [CTCAE] Version 5 Grade 2 or higher) or clinically significant ECG abnormalities
• Screening 12-lead ECG showing a baseline QT interval as corrected by Fridericia's formula (QTcF) >500 msec

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

EMN Trial Office S.r.l. Impresa Sociale

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

AOU Ospedali Riuniti Umberto I

Ancona, , Italy

AOU Policlinico di Bari

Bari, , Italy

AOU di Bologna

Bologna, , Italy

Ospedale di Bolzano - Azienda Sanitaria dell'Alto Adige

Bolzano, , Italy

AOU Policlinico S. Martino

Genova, , Italy

I.R.C.C.S. Ospedale S. Raffaele

Milan, , Italy

AOU Federico II

Napoli, , Italy

AO di Padova

Padua, , Italy

AO di Perugia-Ospedale S. Maria della Misericordia

Perugia, , Italy

Policlinico Umberto I - Università 'Sapienza'

Roma, , Italy

AO S. Maria

Terni, , Italy

AOU Città della Salute e della Scienza di Torino

Torino, , Italy

AOU Ospedali Riuniti di Trieste

Trieste, , Italy

Ospedale S. Maria della Misericordia di Udine

Udine, , Italy

Countries

Italy

Other Identifiers

ISABEL

Identifier Type: -

Identifier Source: org_study_id