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ong-term Follow-up Study for Participants Previously Treated with Ciltacabtagene Autoleucel

Phase 1
Recruiting
Conditions
Multiple Myeloma
MedDRA version: 21.0Level: LLTClassification code: 10028228Term: Multiple myeloma Class: 10029104
Therapeutic area: Diseases [C] - Neoplasms [C04]
Registration Number
CTIS2023-505530-10-00
Lead Sponsor
Janssen - Cilag International
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
365
Inclusion Criteria

All subjects who received cilta-cel in a Company-sponsored clinical study are candidates for Study MMY4002. The inclusion criteria for the study are described below: 1. Subjects who have received at least one dose of cilta-cel in a Company-sponsored clinical study., 2. Subjects who have provided informed consent for Study MMY4002.

Exclusion Criteria

No exclusion criteria are applicable in this study.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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