Isatuximab

SARCLISA®

Overview

Isatuximab is a type of drug called a monoclonal antibody. Isatuximab targets a protein called CD38, which is present in high numbers on the surface of multiple myeloma cells, as well as on certain other types of cells, such as red blood cells.

SparkCures ID 94
Developed By Sanofi
Brand Name Sarclisa®
Generic Name Isatuximab
Additional Names SAR650984
Treatment Classifications
Treatment Targets

Clinical Trials

All Clinical Trials

View all active clinical trials around the US.

Untreated / Newly Diagnosed Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have been newly diagnosed or have not yet received treatment.

Early Relapse Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have received one to two prior lines of therapy.

Late Relapse Multiple Myeloma

The following is a listing of clinical trials for patients with multiple myeloma who have received three or more prior lines of therapy.

Smoldering Myeloma
Monoclonal Gammopathy of Undetermined Significance (MGUS)

The following is a listing of clinical trials for patients with Monoclonal Gammopathy of Undetermined Significance (MGUS).

Published Results

Home administration of isatuximab subcutaneous by on-body injector in Relapsed/Refractory multiple myeloma in the Phase 3 iraklia study

December 09, 2025

Results: In the ongoing IRAKLIA trial, 202 patients were treated with Isa SC OBI within countries where athome administration was permissible. 11 (5.4%) of these patients from 5 different countries [Australia (n=6), Hungary (n=2), Italy (n=1), Norway (n=1), and Spain (n=1)] have participated in home administration as of the cutoff date (06-Nov-2024), with additional sites and countries initiated after the cutoff date. First at home administrations started at Cycle 6 for the majority of patients (n =7) and at Cycle 7 (n =1), Cycle 8 (n =2), and Cycle 10 (n =1) for the remaining patients. Among the 11 patients participating in at-home visits, more than half switched to at-home administration and have not returned to the hospital for their next Day 15 cycle visit. 55 injections were performed at home. The median injection duration was the same between clinic and at-home administration (13 minutes). Similar to Isa SC OBI use in the clinic, home administration was well tolerated with no new safety signals and a 100% completed injection rate. No at-home Isa OBI administration was omitted or interrupted during the injection. At-home administration had a very low rate of injection-site reactions (ISR; n=1). The single ISR was a Grade 1 episode consisting of injection swelling, which resolved within the same day, and most subsequent Day 15 administrations were performed at home for this patient. No other adverse events (AEs), including no IRs, were linked to at-home visits. No device event linked to at-home visits was reported.

Conclusions: Initial data from the ongoing IRAKLIA trial support the safety of at-home administration of Isa SC OBI for the treatment of patients with MM. Home administration was well tolerated, with no safety concerns and a median injection time of 13 minutes consistent with in-clinic use of Isa SC OBI. The option of either home or outpatient administration of Isa SC OBI for patients with MM allows for greater flexibility and accessibility of treatment, with the potential to improve patient care and reduce common barriers to patient retention and therapy compliance.

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