Trial intelligence / Profile preview

FAM BMT in Children With Non-Malignant Disorders

NCT03128996Phase 2Recruiting

Sponsor
Washington University School of Medicine
Start
Mar 2017
Primary completion
Apr 2028
Modality
Monoclonal Antibodies, Orthosteric Ligands, Metabolically Activated Prodrugs
Countries
1
01

Overview

A Phase 2 trial of hydroxyurea, alemtuzumab, fludarabine, thiotepa, melphalan in sickle cell disease (SCD), bone marrow failure syndrome (BMFS), metabolic disorder, immunological diseases (IMD), hemoglobinopathy, sponsored by Washington University School of Medicine. Started Mar 2017; status: recruiting.

02

Drugs

hydroxyureaalemtuzumabfludarabinethiotepamelphalan
03

Conditions

sickle cell disease (SCD)bone marrow failure syndrome (BMFS)metabolic disorderimmunological diseases (IMD)hemoglobinopathy

Beyond the preview

Go deeper on NCT03128996.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on NCT03128996.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call