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Completed

NCT Number: NCT04153279

CMV-TCR-T Cells for CM Virus Infection After HSCT

This is a single cente, single arm, open-label, phase I study to evaluate the safety and effectiveness of CMV-TCR-T cell immunotherapy in treating CMV virus infection after HSCT.

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Key information

Age range

1 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Hebei Yanda Ludaopei Hospital

Sanhe, Hebei, 065200, China

About this study

CMV infection is a common virus infection of HSCT, and which is highly related with the failure of transplantation and survival time of transplant patients. To evaluate the safety and efficacy of allogenic CMV-TCR-T cell therapy in subjects with CMV infection, patients with CMV emias or deseases will be enrolled, and donor derived CMV-TCR-T(HLA-A*1101\\0201\\2402) cells will be intravenously infused with a escalated dose of 0.1-1×106 CMV-TCR-T cells. The CMV DNA copies and CMV-TCR-T cell proliferation will be monitored in the scheduled time (day 0, day 4, day 7, day 10, day 14, day 28).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 1-70 years, including boundary values, gender unlimited;
  • Allogenic hematopoietic stem cell transplantation patients with CMV infection disease or persistent CMV emia;
  • At least one of the following conditions after allogeneic HSCT:
  • After trested with 2-week standard antiviral drug, compared to the baseline of treatment, the decrease of CMV DNA copies number was less than 1log10, and the CMV DNA copies number is greater than 1000 copies/ mL ;
  • Unable to tolerate the toxic and side effects of antiviral drugs,such as bone marrow hematopoietic suppression, nephrotoxicity;
  • Estimated life expectancy ≥3 months;
  • ECOG 3;
  • Patients who voluntarily sign informed consent and are willing to comply with treatment plans, visit arrangements, laboratory tests and other research procedures.

Exclusion criteria

  • Patients with active aGVHD III-IV and / or mild and severe cGVHD;
  • Received cell therapy such as DLI,CTL,CAR-T or participated in any other clinical study of drugs and medical devices before 30 days of enrollment.
  • Pregnant or lactating women;
  • Intracranial hypertension or confusion; respiratory failure; disseminated intravascular coagulation;
  • patients with organ failure:
  • Heart: NYHA heart function grade IV;
  • Liver: Grade C that achieves Child-Turcotte liver function grading;
  • Kidney: kidney failure and uremia;
  • Lung: symptoms of respiratory failure;
  • Brain: a person with a disability;
  • The researchers found that it was unsuitable for the recipients to be enrolled.

Treatment and study plan

CMV-TCR-T cells

Biological

Patients with CMV emias or CMV disease will be enrolled, and donor derived CMV-TCR-T(HLA-A*1101\\0201\\2402) cells will be intravenously infused with a escalated dose of 0.1-1×106 CMV-TCR-T cells. The CMV DNA copies and CMV-TCR-T cell proliferation will be monitored in the scheduled time (day 0, day 4, day 7, day 10, day 14,day 28).

Primary outcomes

  1. Percentage of adverse events

    Time frame: 3months

    Percentage of participants with adverse events.

Secondary outcomes

  1. Persistence of TCR-T cells

    Time frame: 3months

  2. Changes of CMV-DNA copies number

    Time frame: 3months

Sponsors and collaborators

Lead sponsor

Hebei Yanda Ludaopei Hospital

Other

Collaborators

  • China Immunotech (Beijing) Biotechnology Co., Ltd.

Registry information

Official study title

A Pilot Study of CMV-TCR-T Cells in CM Virus Infection Diseases After HSCT

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Nov 6, 2019
Registry last updated
Jan 12, 2023

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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