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Clinical Trial Report
Gene Therapy Trial Report
Summary
Gene Correction in Autologous CD34+ Hematopoietic Stem Cells (HbS to HbA) to Treat Severe Sickle Cell Disease
NCTID
NCT04819841
(View at clinicaltrials.gov)
Description
This study is a first-in-human, single-arm, open-label Phase I/II study of nula-cel in approximately 15 participants, diagnosed with severe Sickle Cell Disease. The primary objective is to evaluate safety of the treatment in this patient population, as well as preliminary efficacy and pharmacodynamic data.
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Development Status
Active
Indication
Sickle Cell Disease
Disease Ontology Term
DOID:0081445
Compound Name
KMAU-001
Compound Alias
nulabeglogene autogedtemcel
Sponsor
Kamau Therapeutics
Funder Type
Industry
Recruitment Status
Recruiting
Enrollment Count
15
Results Posted
Not Available
Therapy Information
Target Gene/Variant
HBB
Therapy Type
Gene editing
Therapy Route
Ex-vivo
Mechanism of Action
Mutation correction
Route of Administration
Intravenous
Drug Product Type
Autologous cells
Target Tissue/Cell
CD34+ cells
Delivery System
Viral transduction
Vector Type
AAV6
Editor Type
Cas9 mRNA
Dose 1
Transduced CD34+ cells
Dose 2
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase1, Phase2
Submit Date
2021-03-24
Completion Date
2027-07-31
Last Update
2025-04-13
Participation Criteria
Eligible Age
12 Years - 40 Years
Standard Ages
Child, Adult
Sexes Eligible for Study
ALL
Locations
No.of Trial Sites
3
Locations
United States
Regulatory Information
Has US IND
True
FDA Designations
Recent Updates
Product was previously developed by Graphite Bio
Resources/Links
Clinical Publications
(Poster) One Year Follow-up on the First Patient Treated with Nula-Cel: An Autologous CRISPR/Cas9HBBGene Corrected CD34+Cell Product to Treat Sickle Cell Disease - ASH 2023
News and Press Releases
A Sickle Sequel: Matthew Porteus Launches Kamau with Positive Nula-Cell Patient Zero Results
Preclinical Publications
Molecular dynamics of genome editing with CRISPR-Cas9 and rAAV6 virus in human HSPCs to treat sickle cell disease
Development of β-globin gene correction in human hematopoietic stem cells as a potential durable treatment for sickle cell disease
Priming Human Repopulating Hematopoietic Stem and Progenitor Cells for Cas9/sgRNA Gene Targeting
CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cells