To Evaluate Long- Term Safety and Efficacy of Luspatercept

NCT06875219 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2025-03-13

No results posted yet for this study

Summary

An observational study to evaluate long-term safety and efficacy of luspatercept in subjects with transfusion dependent who received the first dose of luspatercept after its introduction in the clinical practice

Conditions

  • Thalassemia Major

Interventions

DRUG

Luspatercept (ACE-536)

Luspatercept (ACE-536)

Sponsors & Collaborators

  • Fondazione per la Ricerca sulle Anemie ed Emoglobinopatie in Italia

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-30
Primary Completion
2025-02-24
Completion
2026-02-24

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06875219 on ClinicalTrials.gov