← Eichor
Study identifier: NCT07635693 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ATLG Levels in Autologous HSCT for Multiple Sclerosis

Condition: Multiple Sclerosis · Autologous Hematopoietic Stem Cell Transplant · ATLG  ·  Sponsor: Ciceri Fabio

PhaseN/A
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective, observational, biological, multicenter study to investigate IR profile, ATLG dynamics, main HSCT and disease outcomes in MS. This study will provide a preliminary descriptive evaluation of key study parameters, including ATLG pharmacokinetics and immune reconstitution trends, as well as an initial assessment of variability (e.g., dispersion of immunological biomarkers), to support the interpretation of results and the design of future studies. Since this is an observational study, no clinical decision will be made, and the interim analysis will not have an impact of the study conduction, and it will not be a stopping rule.

This description comes directly from the study's public registry record.

Talk to the study team

Raffaella Greco  ·  +39 02-2643-3903  ·  greco.raffaella@hsr.it

Always discuss trial participation with your own doctor first.

Locations (1)

IRCCS Ospedale San RaffaeleMilan, Italy, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07635693