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Monoclonal Antibodies

Alemtuzumab for Sickle Cell Disease

Phase < 1
Waitlist Available
Led By Kathleen Dorritie, MD
Research Sponsored by Kathleen Dorritie
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 100 days after hsct
Awards & highlights

Study Summary

This trial is testing a new stem cell transplant treatment for sickle cell disease using a matched donor.

Eligible Conditions
  • Sickle Cell Disease

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 100 days after hsct
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 100 days after hsct for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Treatment Success
Secondary outcome measures
Changes in monthly transfusions after HSCT
Changes in the annual frequency of SCD-related hospitalization after
Therapeutic immunosuppression
+10 more

Side effects data

From 2017 Phase 4 trial • 8 Patients • NCT01395316
13%
Hypothyroidism
100%
80%
60%
40%
20%
0%
Study treatment Arm
Alemtuzumab

Trial Design

1Treatment groups
Experimental Treatment
Group I: Non Myeloablative regimen (Alemtuzumab)Experimental Treatment3 Interventions
Sickle cell patient receives sibling donor peripheral blood stem cell transplant with non-myeloablative pre-transplant conditioning.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Alemtuzumab
2004
Completed Phase 4
~1890
Total Body Irradiation
2006
Completed Phase 3
~820
Sirolimus
2013
Completed Phase 4
~2750

Find a Location

Who is running the clinical trial?

Kathleen DorritieLead Sponsor
1 Previous Clinical Trials
34 Total Patients Enrolled
Kathleen Dorritie, MDPrincipal Investigator - UPMC Hillman Cancer Center
University of Pittsburgh

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~0 spots leftby Apr 2025