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NCT Number: NCT04390971

Safety and Efficacy Evaluation of ET-01 Transplantation in Subjects With Transfusion Dependent β-Thalassaemia

This is an open label, multi-center study to evaluate the safety and Efficacy of ET-01 Transplantation in subjects with Transfusion Dependent β-Thalassaemia.

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Key information

Age range

6 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China

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About this study

After the proper subject is recruited, subject will go through steps generally as stem cell mobilization, apheresis, conditioning and ET-01 infusion to complete therapy. Two years follow-up will be carried out post-transplantation and related data will be collected. Subjects who have been treated by ET-01 will be asked to participate in a long-term follow up study. Monitoring the long-term efficacy and safety up to 15 years after ET-01 transplant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject and/or subject's legal personal representative fully understand and voluntarily sign informed consent forms;
  • 6~35 years old, all gender;
  • Diagnosis of transfusion dependent β-thalassemia (β-TDT) as defined by protocol;
  • Eligible for autologous stem cell transplant;
  • Eligible for autologous stem cell transplant;
  • Organs in good function.
  • Other protocol defined inclusion criteria may apply.

Exclusion criteria

  • Subjects with associated α-thalassemia;
  • Active bacterial, virus, fungal or parasitic infection, including HIV infection, HbsAg and HBV DNA positive, HCV DNA positive, or Treponema Pallidum infection;
  • HLA identical sibling or unrelated donors are available;
  • Prior allo-HSCT or gene therapy.
  • Other protocol defined exclusion criteria may apply.

Treatment and study plan

ET-01

Biological

Recruited participants will receive ET-01 IV infusion after conditioning.

Primary outcomes

  1. Frequency and severity of AEs & SAEs identified according to NCI CTCAE 5.0.

    Time frame: From ET-01 infusion to 104 weeks post-transplant

  2. All-cause mortality

    Time frame: From signing of informed consent to 104 weeks post-transplant

  3. Incidence of transplant-related mortality

    Time frame: Within 100 days post-transplant

  4. Proportion of subjects with engraftment

    Time frame: Up to 42 days post-transplant

Secondary outcomes

  1. Change of total hemoglobin from baseline

    Time frame: Within 104 weeks post-transplant

  2. Change of HbF from baseline

    Time frame: Within 104 weeks post-transplant

  3. Change of proportion of HbF/Hb

    Time frame: Within 104 weeks post-transplant

  4. Change of frequency of packed RBC transfusions

    Time frame: From 6 months before recruitment to 104 weeks post-transplant

  5. Change of volume of packed RBC transfusions

    Time frame: From 6 months before recruitment to 104 weeks post-transplant

Sponsors and collaborators

Lead sponsor

Institute of Hematology & Blood Diseases Hospital, China

Other

Collaborators

  • EdiGene Inc.
  • The Affiliated Hospital Of Guizhou Medical University
  • Zunyi Medical College

Registry information

Official study title

A Multi-center, Open Label Study to Evaluate the Safety and Efficacy of ET-01 Transplantation in Subjects With Transfusion Dependent β-Thalassemia

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
May 18, 2020
Registry last updated
Feb 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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