Primary Objectives: Part A: To evaluate the safety and determine the recommended dose of SAR650984 in combination with pomalidomide (P) and dexamethasone (d), in patients with Relapsed/Refractory Multiple Myeloma (RRMM). Part B: To evaluate the feasibility of isatuximab administered from a fixed infusion volume in combination with Pd as assessed by occurrence of grade ≥3 infusion associated reactions (IAR). Secondary Objectives: * To evaluate the infusion duration (Part B). * To evaluate the safety profile of the combination with isatuximab administration from fixed volume (Part B). * To evaluate immunogenicity of SAR650984 in combination with Pd (Part A and B). * To evaluate the pharmacokinetics (PK) of SAR650984 and its effect on the PK of pomalidomide when administered in combination (Part A). * To describe the efficacy of the combination of SAR650984 with Pd in terms of overall response rate and clinical benefit rate based on International Myeloma Working Group (IMWG) defined response criteria and the duration of response (Part A and B). * To assess the relationship between clinical effects (adverse event \[AE\] and/or tumor response) and CD38 receptor density at baseline (Part A).
The study duration for an individual patient will include a screening period for inclusion of up to 21 days. The treatment period may continue until disease progression, unacceptable adverse reaction, or other reason for discontinuation. After study treatment discontinuation an end of treatment (EOT) visit will be done at approximately 30 days after last study treatment component administration to assess safety. If the last ADA sample is positive or inconclusive, additional ADA will be sampled 3 months later. No further ADA will be sampled, even if this 3-month sample is positive. Patients who discontinue treatment for reasons other than progression of disease will be followed every month until progression or initiation of subsequent therapy, for a maximum of one year, whichever comes first.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
54
Pharmaceutical form:solution for infusion Route of administration: intravenous
Pharmaceutical form:capsules Route of administration: oral
Pharmaceutical form:tablets or solution for infusion Route of administration: oral or intravenous
Investigational Site Number 840001
Scottsdale, Arizona, United States
Investigational Site Number 840006
Duarte, California, United States
Investigational Site Number 840018
New Haven, Connecticut, United States
Investigational Site Number 840011
Decatur, Illinois, United States
Investigational Site Number 840004
Boston, Massachusetts, United States
Investigational Site Number 840104
Boston, Massachusetts, United States
Investigational Site Number 840010
Chapel Hill, North Carolina, United States
Investigational Site Number 840003
Charlotte, North Carolina, United States
Investigational Site Number 840014
Canton, Ohio, United States
Investigational Site Number 840016
Charleston, South Carolina, United States
...and 3 more locations
Dose Limiting Toxicities (DLTs)
Time frame: Part A: Up to 4 weeks
Number of patients with adverse events and clinically significant changes in laboratory tests and vital signs according to the National Cancer Institute - Common Toxicity Criteria (NCI-CTC) version 4.03 grade scaling
Time frame: Part A: Up to 30 days for patients experiencing progressive disease and up to one year or the initiation of a new line of treatment for patients leaving the study for reasons other than progressive disease
Incidence of grade ≥3 IARs according to the NCI-CTC version 4.03 grade scaling
Time frame: Part B: Up to 8 weeks
Overall response rate
Time frame: Part A: Up to approximately 8 months; Part B: Up to approximately 10 months
Pharmacokinetics: Partial area under the serum concentration time curve (AUC)
Time frame: Part A: Up to approximately 10 months
Pharmacokinetics: maximum observed concentration (Cmax)
Time frame: Part A: Up to approximately 10 months
Immune response: levels of human anti-human antibodies (ADA)
Time frame: Part A: Up to approximately 8 months; Part B: Up to approximately 10 months
Duration of response - Time
Time frame: Part A: Up to approximately 8 months; Part B: Up to approximately 10 months
Clinical Benefit rate
Time frame: Part A: Up to approximately 8 months; Part B: Up to approximately 10 months
Infusion duration
Time frame: Part B: Up to approximately 10 months
Safety of isatuximab administration from fixed volume
Time frame: Part B: Up to 30 days for patients experiencing progressive disease and up to one year or the initiation of a new line of treatment for patients leaving the study for reasons other than progressive disease
Relationship between clinical effect and CD38 receptor density
Time frame: Part A: Up to approximately 8 months
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