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This study is to fulfil the regulatory requirement for 15-year follow-up for patients treated with MB-105 in any study
Full description
This study is for long term follow up of efficacy and safety for any patient treated with MB-105 who has consented to joining the LTFU study. There are no exclusion criteria.
Enrollment
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Volunteers
Inclusion criteria
Received MB-105 Signed informed consent Agree to transfer of samples from previous study Able to comply with study requirements
Exclusion criteria
N/A
40 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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