EDIT-301: Phase 1/2 Sickle Cell Disease Gene Therapy Trial

AddtoAny
Share:

WATCH THIS PAGE

Subscribe to be notified of changes or updates to this page.

2 + 4 =
Solve this simple math problem and enter the result. E.g. for 1+3, enter 4.

Individuals with severe sickle cell disease, who are between 18 and 50 years old, may be able to participate. A number of screening tests will be done to determine if subjects can participate. These include review of your past medical history, physical exam, blood and urine tests, pregnancy test, heart ultrasound, electrocardiogram, pulmonary function test, kidney function test, questionnaires, and magnetic resonance imaging (MRI) of the heart and liver. If eligible, blood stem cells will be collected by apheresis. A gene in these stem cells will then be edited to help the stem cells make more fetal hemoglobin. Higher levels of fetal hemoglobin can improve red blood cell sickling. You will then be hospitalized and chemotherapy will be given to empty out the bone marrow. The stem cells, with the modified gene, will then be given back to you. You will be followed for side effects and to see if the modified gene helps you make healthy red blood cells.

Who Do I Contact?

If you are interested in participating in the study or want to learn more please contact our study team at hamiltonca [at] chop.edu or 267-601-3461.

Eligibility & Criteria

IRB #:
21-018408
Official Title:
A Phase 1/2 Study to Evaluate the Safety and Efficacy of a Single Dose of Autologous Clustered Regularly Interspaced Short Palindromic Repeats Gene-edited CD34+ Human Hematopoietic Stem and Progenitor Cells (EDIT-301) in Subjects with Severe Sickle Cell Disease
Study Phase:
Phase I
Phase II
Eligible Age Range:
18 - 50 Years
Gender:
All
Study Categories: