Clinical Trials Directory

Trials / Completed

CompletedNCT02268409

Extension Study to Evaluate the Safety and Efficacy of Luspatercept in Participants With β-Thalassemia Previously Enrolled in A536-04 (A536-06/MK-6143-004)

An Open-Label Extension Study To Evaluate The Long-Term Effects Of ACE-536 In Patients With β-Thalassemia Previously Enrolled In Study A536-04

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
51 (actual)
Sponsor
Acceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway, NJ USA · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Study A536-06 (MK-6143-004) is an open-label extension study for participants previously enrolled in study A536-04 (NCT01749540), to evaluate the long-term safety and tolerability of luspatercept in adult participants with beta-thalassemia.

Conditions

Interventions

TypeNameDescription
DRUGluspaterceptsubcutaneous injection

Timeline

Start date
2014-10-20
Primary completion
2020-06-18
Completion
2020-06-18
First posted
2014-10-20
Last updated
2024-07-18
Results posted
2024-07-18

Locations

7 sites across 2 countries: Greece, Italy

Source: ClinicalTrials.gov record NCT02268409. Inclusion in this directory is not an endorsement.

Extension Study to Evaluate the Safety and Efficacy of Luspatercept in Participants With β-Thalassemia Previously Enroll (NCT02268409) · Clinical Trials Directory