A Study to Assess the Safety, Tolerability, and Efficacy of ST-400 for Treatment of Transfusion-Dependent Beta-thalassemia (TDT)

a study on Transfusion Dependent Beta-thalassemia

Summary

for people ages 18–40 (full criteria)
at Oakland, California
study started
estimated completion:

Description

Summary

This is a single-arm, multi-site, single-dose, Phase 1/2 study to assess ST-400 in 6 subjects with transfusion-dependent β-thalassemia (TDT) who are ≥18 and ≤40 years of age. ST-400 is a type of investigational therapy that consists of gene edited cells. ST-400 is composed of the patient's own blood stem cells which are genetically modified in the laboratory using Sangamo's zinc finger nuclease (ZFN) technology to disrupt a precise and specific sequence of the enhancer of the BCL11A gene (which normally suppresses fetal hemoglobin production in erythrocytes). This process is intended to boost fetal hemoglobin (HbF), which can substitute for reduced or absent adult (defective) hemoglobin, and is done without the use of integrating viral vectors. ST-400 is then infused back into the patient after receiving conditioning chemotherapy to make room for the new cells in the bone marrow, with the aim of producing new erythrocytes with increased amounts of HbF. The primary objective is to understand safety and tolerability of ST-400, and secondary objectives are to assess the effects on HbF levels and transfusion requirements.

Official Title

A Phase 1/2, Open-label, Single-arm Study to Assess the Safety, Tolerability, and Efficacy of ST-400 Autologous Hematopoietic Stem Cell Transplant for Treatment of Transfusion-Dependent Beta-thalassemia (TDT)

Details

Once consented, study participants will progress through the following stages:

  • Screening: in-person visit at the study site to confirm eligibility for proceeding
  • Collection: autologous (self) blood stem cells are harvested at the study site, also known as apheresis
  • Manufacturing of ST-400: no study participant activities expected
  • Infusion: conditioning chemotherapy, followed by infusion of ST-400, occurs at the study site
  • Follow-up: follow up at the study site to monitor for safety and effectiveness of the study

Keywords

Transfusion Dependent Beta-thalassemia Beta thalassemia Beta-thalassemia Thalassemia major Cooley's anemia ZFN mediated genome editing zinc finger nuclease Thalassemia

Eligibility

You can join if…

Open to people ages 18–40

  1. Informed Consent
  2. Clinical diagnosis of TDT with ≥ 8 documented RBC transfusion events per year on an annualized basis in the 2-years prior to screening
  3. Confirmed beta-thalassemia diagnosis by molecular genetic testing
  4. Clinically stable and eligible to receive conditioning chemotherapy
  5. Able and willing to use double barrier method of contraception for at least 3 months prior to ST-400 infusion and through 6 months post-transplant

You CAN'T join if...

  1. Previous history of autologous or allogeneic blood stem cell transplantation or solid organ transplantation
  2. Pregnant or breastfeeding female
  3. Medical contraindication to apheresis
  4. Significant liver, lung, heart, or kidney dysfunction
  5. Diagnosis of HIV or evidence of active HBV or HCV
  6. History of significant bleeding disorder or uncontrolled seizures
  7. History of active malignancy in past 5 years (non-melanoma skin cancer or cervical cancer in situ permitted)
  8. Currently participating in another clinical trial using an investigational study medication, or recent participation in such a trial
  9. Previous treatment with gene therapy

Location

  • UCSF Benioff Children's Hospital Oakland accepting new patients
    Oakland, California, 94609, United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Sangamo Therapeutics
ID
NCT03432364
Phase
Phase 1/2
Lead Scientist
Mark Walters
Study Type
Interventional
Last Updated
March 27, 2018
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