CS-101 in Patients With β-thalassemia

Official title

A Clinical Study Evaluating the Safety and Efficacy of Autologous Peripheral Blood Hematopoietic Stem and Progenitor Cells (CS-101) Modified by Ex Vivo Base Editing to Induce γ-Globin Production in Treating Patients With β-Thalassemia

Overview

The goal of this open label, single-arm clinical study is to learn about the safety and efficacy of CS-101 in treating β-thalassemia.

Detailed description

CS-101 is an autologous CD34+ cell suspension, edited by in vitro base editing technology, which modifies the BCL11A binding site in HBG promoter, so that it loses the ability to bind to BCL11A, which can re-induce the production of γ-globin chain and increase the concentration of fetal hemoglobin(HbF) in the blood, compensating for the function of missing adult hemoglobin HbA to achieve clinical cure. The therapy addresses two major challenges in the current treatment of the disease: lack of matching donors and graft-versus-host diseases in allogeneic hematopoietic stem cell transplantation.

Interventions

• Genetic CS-101
  Autologous CD34+ hematopoietic stem cell suspension modified by in vitro base editing technique

Primary outcome measures

• Frequency and severity of adverse events(AEs）as assessed by CTCAE v5.0 [Time frame: From signing informed consent to 12 months post-CS-101 infusion]
• Time to neutrophil and platelet engraftment [Time frame: Days post-CS-101 infusion]
• Proportion of subjects with engraftment [Time frame: within 42 days post-CS-101infusion]
• Incidence of transplant-related mortality [Time frame: From baseline to 100 days post-CS-101 infusion]
• All-cause mortality [Time frame: From signing informed consent to 12 months post-CS-101 infusion]
• Proportion of subjects achieving transfusion independence for at least 6 consecutive months [Time frame: From 3 months up to 12 months post-CS-101 infusion]
• Time to last red blood cell(RBC) transfusion [Time frame: Days post-CS-101 infusion]

Secondary outcome measures (3)

• Change in total hemoglobin(Hb) concentration over time [Time frame: up to 12 months post-CS-101 infusion]
• Change in fetal hemoglobin(HbF) concentration over time [Time frame: up to 12 months post-CS-101 infusion]
• Chimerism level in Peripheral blood and bone marrow [Time frame: up to 12 months post-CS-101 infusion]

Eligibility criteria

Inclusion criteria

• 6 to 35 years old(inclusive) male or female subjects at the time of informed consenting Diagnosis of β-thalassemia, genotypes include but are not limited to β+β0，βEβ0，β0β0, etc History of at least≥8 units/year of packed RBC transfusions in the prior 12 months prior to the screening period Generally in good condition, Karnofsky performance score≥60 points for subjects≥16 years old at the time of autologous hematopoietic stem cell collection, or Lansky Play-Performance score≥60 points for subjects under 16 years old, or equivalent clinical evaluation as the investigator site's common practice

Exclusion criteria

• Treatment with other investigational medications or other experimental interventions 30 days prior to signing informed consent or within 6 half-lives of the drug, whichever is longer.

Subjects who have received or are receiving thalidomide and/or Luspatercept, when their drug-drug interaction on the efficacy and safety of CS-101 cannot be ruled out, unless at least there are 3 test results showing the total hemoglobin level before transfusion is below 9g/dL in the past 6 months before screening.

Previously received allogeneic hematopoietic stem cell transplantation or gene(edited) therapy.

Subjects have available related fully matching donors and are eligible and prepared for allogeneic hematopoietic stem cell transplantation.

Those with active infections, including but not limited to: HIV, hepatitis B, hepatitis C, cytomegalovirus, Epstein-Barr virus and treponema pallidum test positive, or known tuberculosis, parasitic infection, etc. who are judged by the investigator to be unsuitable to participate in this study.

Echocardiography results with ejection fraction below 45%. Advanced liver disease, defined as：

Aspartate aminotransferase (AST), alanine aminotransferase (ALT) >3 × upper limit of normal (ULN) or:

Baseline International Normalized Ratio (INR) >1.5 × ULN.

MRI during the screening period showed heavy iron overload and is judged by the investigator to be unable to participate in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• The First Affiliated Hospital of Guangxi Medical University — Nanning

Identifiers

NCT: NCT06328764 · CS-101-11

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗