CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 8 enrolled
Drug / intervention
MGTA-456drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03406962
NCT03406962Phase 2Completed

A Phase 2, Single-arm, Open-label Study to Evaluate the Safety and Efficacy of MGTA-456 in Patients With Inherited Metabolic Disorders (IMD) Undergoing Hematopoietic Stem Cell Transplantation (HSCT)

Magenta Therapeutics, Inc.·interventional·Posted Jan 23, 2018·Updated Nov 3, 2021

In Brief

A Phase 2 clinical trial evaluating MGTA-456 for Inherited Metabolic Disorders (IMD). Completed, enrolled 8 participants across 2 sites.

Detailed Summary

This study is designed to assess the safety and efficacy of using MGTA-456 in patients with Inherited Metabolic Disorders (IMD) undergoing stem cell transplantation.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedJan 23, 2018
Enrollment StartFeb 9, 2018
Primary CompletionFeb 10, 2020
Study CompletionJan 15, 2021
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 8.4 years ago

Interventions

MGTA-456drug

Hematopoietic stem cell transplantation will be done with the cell therapy product MGTA-456.