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

Phase 4
Conditions
Multiple Myeloma
plasma cell myeloma
10040778
Registration Number
NL-OMON53393
Lead Sponsor
Janssen-Cilag International NV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
6
Inclusion Criteria

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
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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