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RecruitingNCT06052436THYTECH2Updated Sep 18, 2026

Cell Therapy With Treg Cells Obtained From Thymic Tissue (thyTreg) to Control the Immune Hyperactivation Associated With COVID-19 and/or Acute Respiratory Distress Syndrome (THYTECH2)

A Phase 1/2 interventional study of Allogeneic thyTreg 5.000.000 and Allogeneic thyTreg 10.000.000 in Systemic Inflammatory Response Syndrome, sponsored by Hospital General Universitario Gregorio Marañon. Recruiting at 1 site in Spain. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by Hospital General Universitario Gregorio Marañon · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
24
Allocation
Non-randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The investigators developed a GMP protocol to isolate Treg cells from thymic tissue (thyTreg). The thyTreg cells are being evaluated in a Phase I/II clinical trial to evaluate the safety and efficacy of the adoptive transfer of autologous thyTreg to prevent rejection in heart transplant children (NCT04924491), with preliminary results indicating the feasibility and safety of the therapy.

In addition, thyTreg cells have shown low immunogenicity in the pre-clinical setting, indicating that allogeneic use of these thyTreg cells (allo-thyTreg) would have a low risk of adverse effects. These thyTreg cells could inhibit an excessive inflammation in SARS-CoV-2 infection, or ameliorate the immunological affection underlying Acute respiratory distress syndrome, improving life-threatening manifestations, restoring immune balance, and protecting affected tissues.

This clinical trial is an open-label Sequential Parallel Group Phase I/II study to evaluate the safety and efficacy of allogeneic thymus derived Tregs (thyTreg) (thyTreg) in controlling the immune dysregulation associated with SARS-CoV-2 infection and/or Acute Respiratory Distress Syndrome.

Read the detailed description

The immune system is the body's defense system against pathogens and other harmful agents, but it is also responsible for transplant rejection or autoimmune diseases. Another scenario of disproportionate immune response is the Immune Hyperactivation, an exaggerated systemic inflammatory response such as that caused by respiratory infections like COVID-19, a major cause of acute respiratory distress syndrome (ARDS) in critically ill patients.

The standard treatment to prevent these immune responses is the use of immunosuppressive and immunomodulatory therapy, which produces a pleotropic inhibition on the immune system and have a high cost. However, a widespread feeling among the scientific community is that only re-educating immune system to promote immune tolerance will decline the harmful immune responses without prejudice to the functional integrity of the immune system.

In the context of severe COVID-19 and ARDS, it has been shown that an alteration in the frequency and functionality of Tregs. In addition, it has been described that the increased oxygen therapy requirements is not due to the viral effect, but to the triggered immune hyperinflammation that can lead to multi-organ failure and death. Therefore, although the adoptive transfer of Treg is a promising cell therapy for the treatment of this type of disease, the characteristics of the patients make it unfeasible to obtain enough Treg from the patient to produce a therapeutic dose and, if achieved, the quality of these cells does not allow a prolonged therapeutic effect to be obtained over time.

Tregs are a subset of CD4+ T cells with suppressive function that maintain the immune system balance. Adoptive Treg cell therapy has shown efficacy in a variety of immune-mediated diseases in preclinical and clinical studies. To date, most of the clinical trials employing Treg cell therapy have been limited due to a small Treg numbers obtained (Treg cells represent less than 10% of CD4+ T cells) and the low quality of infused Treg (in terms of purity, survival, and suppressor capacity).

The investigators have developed an innovative Treg manufacturing protocol, that overcome the existing difficulties by employing a new source of cells, which is the thymic tissue routinely removed and discarded in paediatric cardiac surgeries. The protocol allows to produce massive amounts of thymus derived Treg cells (thyTreg), with improved survival, high suppressive capacity and suitable for therapeutic use.

The study will evaluate escalating doses of thyTreg administrated as a single IV dose. The study will include up to 2 cohorts of 4 to 8 subjects per each arm (control group and thyTreg group) followed for a total of 24 months. All subjects will receive standard of care treatment for COVID-19 or ARDS, including dexamethasone and other approved therapies from institutional guidelines.

02

Conditions studied

  • Systemic Inflammatory Response Syndrome

Keywords

  • Immune Hyperactivation
  • Regulatory T cell
  • ARDS
  • COVID-19
  • Advanced therapy
  • Immunotherapy
  • Th1-Th2 Balance
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patient over 18 to 65 years of age
  2. Patient Informed and non-opposed to the research by his medical doctor during hospitalization
  3. Patient with clinical, radiological, gasometric and immunological criteria defined as:

    1. Acute respiratory failure secondary to acute lung injury of noncardiogenic cause
    2. Pulmonary abnormalities compatible with bilateral alveoloinsterstitial infiltrates by chest imaging (radiograph or scan)
    3. PaO2/FiO2≤ 300 Presence of at least one of the following markers of inflammation: IL6 > 40 pg/ml or ferritin >300 ng/ml or CRP >3 mg/dl or increasing over the last 24 hours

Exclusion criteria

Exclusion Criteria:

  1. Pregnancy or breast feeding
  2. Body mass index >35
  3. Patients not expected to survive 48 hours after enrolment based on clinical assessment
  4. Patients with an extracorporeal respiratory support
  5. Neutropenia (absolute neutrophil count \<1000/uL)
  6. Thrombocytopenia (absolute neutrophil count \<50000/uL)
  7. Positive serology for HBV, HCV, or HIV at Screening
  8. Life expectancy of less than 6 months due to other pathologies
  9. History of significant underlying pulmonary disease requiring oxygen therapy prior to inclusion.
  10. Patients with a history of autoimmune diseases
  11. Patients with a history of hematopoietic neoplasia or oncology disease
  12. Patients with a history of hematopoietic or solid organ transplant
  13. Patients with a congenital or induced immunodeficiency
  14. Patients received thymoglobulin, basiliximab or any anti-T-cell therapies within 6 moths prior to the screening visit
  15. Patients received other cell therapy in the last 12 months
  16. Patients received intravenous immunoglobulin (IVIg) within 5 moths prior to the screening visit
  17. Patients who have participated or is participating in a clinical research study evaluating COVID-19 or ARDS within 30 days prior to the screening visit
04

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Phase A: 5.000.000 thyTreg /kg

    Allogeneic thyTreg 5.000.000

    Biological: Allogeneic thyTreg 5.000.000

  • No intervention
    Phase A: standard of care

    Standard of care

  • Experimental
    Phase B: 10.000.000 thyTreg /kg

    Allogeneic thyTreg 10.000.000

    Biological: Allogeneic thyTreg 10.000.000

  • No intervention
    Phase B: standard of care

    Standard of care

Interventions

  • BiologicalAllogeneic thyTreg 5.000.000

    Treg lymphocytic cells, differentiated, allogeneic, of thymic tissue, expanded and stimulated with Interleukin (IL-) 2 (thyTreg)

    Also known as: Allogeneic thyTreg cells

  • BiologicalAllogeneic thyTreg 10.000.000

    Treg lymphocytic cells, differentiated, allogeneic, of thymic tissue, expanded and stimulated with Interleukin (IL-) 2 (thyTreg)

    Also known as: Allogeneic thyTreg cells

05

What researchers measure

Primary outcomes

  1. 1. Incidence of infusion-related adverse events (safety) by type, frequency, severity, and causality

    Time frame: 24 months

Secondary outcomes

  1. Length of intensive care unit stay

    Time frame: 24 months

  2. Oxygenation improvement as assessed using PaO2/FiO2 and/or SaO2/FiO2

    Time frame: 24 months

  3. Change in clinical status as assessed using Sequential Organ Failure Assessment Score

    Time frame: 24 months

  4. Change in clinical status as assessed using Acute Physiology and Chronic Health disease Classification System (APACHE) III

    Time frame: 24 months

  5. Change in clinical status as assessed using Barthel score

    Time frame: 24 months

  6. Change in myocardial function as measured by mitral and tricuspid regurgitation using doppler echocardiography

    Time frame: 24 months

  7. Change in myocardial function as measured by mitral and tissue mitral doppler using doppler echocardiography

    Time frame: 24 months

  8. Change in myocardial function as measured by tricuspid and tissue tricuspid using doppler echocardiography

    Time frame: 24 months

  9. Change in SARS-CoV-2 positivity or etiology of ARDS assessed using diagnostics test

    Time frame: 24 months

  10. Change From Baseline in ferritin parameter

    Time frame: 24 months

  11. Change From Baseline in interleukin 6 (IL-6)

    Time frame: 24 months

  12. Change From Baseline in C-Reactive Protein (PCR)

    Time frame: 24 months

  13. Change From Baseline in Treg cells number in peripheral blood

    Time frame: 24 months

  14. Number of T cells, B cells, NK cells, monocytes, dendritic cells, and granulocytes in peripheral blood

    Time frame: 24 months

  15. Change From Baseline in cytokines levels of interferon gamma, tumor necrosis factor alpha and interleukins (IL-6 and IL-10).

    Time frame: 24 months

  16. Overall patient survival rate at 24 months

    Time frame: 24 months

06

Study locations

1 of 1 sites recruiting
  • Hospital General Universitario Gregorio Marañon
    Madrid, Madrid 28007, Spain
    • Rafael Correa-Rocha, PhD · Contact · rafael.correa@iisgm.com · +34 915866455
    • Marta Martínez-Bonet, PhD · Sub investigator
    • Marjorie Pion, PhD · Sub investigator
    • Esther Bernaldo-de-Quirós, PhD · Sub investigator
    • Diana Hernández-Flórez, PhD · Sub investigator
    • María Abad Ferry, MsC · Sub investigator
    • Beatriz Cózar Fernández, MsC · Sub investigator
    • Sergio Gil Manso, PhD · Sub investigator
    • Rocio López Esteban · Sub investigator
    • José Eugenio Guerrero Sanz, MD PhD · Sub investigator
    • Carmen Martínez Mata, MD · Sub investigator
    • Juan Miguel Gil-Jaurena, MD · Sub investigator
    • Carlos Pardo, MD PhD · Sub investigator
    • Ramón Pérez-Caballero, MD PhD · Sub investigator
    • Ana Pita, MD · Sub investigator
    • Mª Eugenia Fernández-Santos, PhD · Sub investigator
    • José Luis Vicario Moreno, PhD · Sub investigator
    Recruiting
07

Registry details

Key details

Study ID
NCT06052436
Lead sponsor
Hospital General Universitario Gregorio Marañon
Collaborators
Instituto de Salud Carlos III
Responsible party
Rafael Correa-Rocha (Principal Investigator, Hospital General Universitario Gregorio Marañon) — Principal investigator
First posted
Sep 25, 2023
Start date
Jun 27, 2023
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Sep 18, 2026

Study contacts

Marta Martínez-Bonet, PhD
Contact
marta.mbonet@iisgm.com
34 915866455
Diana Hernández Flórez, PhD
Contact
diana.hernandez@iisgm.com
34 915866455
Rafael Correa-Rocha, PhD
principal investigator · Hospital General Universitario Gregorio Marañon

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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