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International, multi-center, open-label, treatment extension study in patients with multiple myeloma who are still benefitting from isatuximab-based therapy following completion of a Phase 1, 2, or 3 parental study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507180-19-00
Acronym
LTS17704
Enrollment
37
Registered
2024-04-15
Start date
2023-04-05
Completion date
Unknown
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief summary

Number of participants with treatment-emergent adverse events

Interventions

DRUGMONTELUKAST
DRUGImnovid 2 mg hard capsules
DRUGDIPHENHYDRAMINE
DRUGPARACETAMOL
DRUGMETHYLPREDNISOLONE
DRUGLIBTAYO 350 mg concentrate for solution for infusion.
DRUGRevlimid 25 mg hard capsules
DRUGImnovid 3 mg hard capsules
DRUGRevlimid 10 mg hard capsules
DRUGRevlimid 15 mg hard capsules
DRUGDEXAMETHASONE BASE
DRUGRevlimid 5 mg hard capsules
DRUGImnovid 1 mg hard capsules
DRUGKyprolis 60 mg powder for solution for infusion
DRUGIsatuximab
DRUGDexamethason 4 mg JENAPHARM®
DRUGImnovid 4 mg hard capsules

Sponsors

Sanofi-Aventis Recherche & Developpement
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Number of participants with treatment-emergent adverse events

Countries

Czechia, Finland, France, Greece, Italy, Spain, Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026