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Treatment of Presymptomatic (Stage 1) Type 1 Diabetes Pediatric Patients With Treg Cell Preparations and Anti-CD20 Antibody (PreTreg)

P

PolTREG S.A.

Status and phase

Enrolling
Phase 2

Conditions

Diabetes Mellitus, Type 1
Diabetes Mellitus, Type I
Presymptomatic Diabetes Type 1 (Stage 1)

Treatments

Other: Placebo
Biological: Anti-CD20 (rituximab)
Other: Treg sham
Biological: ex vivo expanded CD4+CD25+CD127- regulatory T cells (Tregs)

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06688331
PTG007-DM1-preTREG-001
2023-505226-33-00 (EU Trial (CTIS) Number)

Details and patient eligibility

About

The main purpose of the study is to check:

  • Can therapy with a preparation of regulatory cells (Tregs lymphocytes) and/or an anti-CD20 antibody preparation (rituximab) be successfully used in children with pre-diabetes to treat or delay type 1 diabetes?
  • Is therapy with a preparation of regulatory cells (Tregs lymphocytes) and/or a preparation of antiCD20 antibodies (rituximab) safe for children with pre-diabetes, and what side effects may be associated with it? The study will include patients at high risk for type 1 diabetes whose laboratory tests have confirmed preserved normal/high insulin production. First (part 1 of the study), tests will be performed to determine the risk of the disease (determination of autoantibodies that characterize the autoimmune background).

In order to confirm the effectiveness of the therapy, not all patients will receive the study treatment. The study will be a so-called blinded randomized trial. This means that in this trial, all participants will undergo the same study procedures, but the participant will be randomly assigned to one of four (4) groups that will receive different treatment regimens before entering the study.

The participant will be randomly assigned to one of four groups:

  • Group I will receive a preparation of regulatory cells (Tregs lymphocytes) along with a preparation of antiCD20 antibodies,
  • Group II will receive a preparation of regulatory cells (Tregs lymphocytes) together with an inert substance (placebo)
  • Group III will receive a preparation of antiCD20 antibodies along with a sham treatment (inert substance)
  • Group IV will receive an agent containing an inert substance and sham treatment.

Approximately 150 patients aged 6-16 who are at risk of developing type 1 diabetes will be enrolled in the study, which will last up to 96 months. Each enrolled participant will remain in the study for up to five years.

Full description

Participants: screening of approximately 2500 high-risk subjects will be conducted until no less than 150 participants with confirmed stage 1 (preclinical) type 1 diabetes mellitus are randomized; randomization 2:1:1:2; 50 participants treated with Tregs and anti-CD20 antibody; 25 participants treated with Tregs; 25 participants treated with anti-CD20 antibody; control: 50 participants receiving placebo and sham Tregs.

Inclusion of participants: up to 36 months. Trial intervention: Total duration of the trial intervention for each participant will be approximately 3 Months. After completion of the trial intervention, participants will be monitored at the sites for the onset of type 1 diabetes mellitus for a maximum of five years counting from the first dose of Tregs.

Follow-up time: post-treatment observation of all participants to 57 months (day "0" is the day of administration of the first dose of Treg/sham preparation).

Trial time: 96 months. Trial type: Prospective randomized (phase 2), placebo-controlled, parallel group, blinded trial.

Blinding: The following roles indicated below will not be made aware of the treatment group assignment during the trial:

  • participant
  • legal representatives
  • site staff excluding pharmacists (applies to anti-CD20only)

Enrollment

150 estimated patients

Sex

All

Ages

6 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Age 6-16

  2. 25 ≤ BMI ≤ 75 percentile (acc. to OLAF) with a lower weight threshold of 20 kg

  3. Venous plasma glucose levels < 100mg% at fasting (70 to 100 mg/dl) and normal glucose tolerance test (at 120 minutes glycaemia <140 mg/dl) (acc. to PTD)

  4. Insulin independence

  5. C-peptide levels ≥ 1.0 ng/ml (central laboratory limit of normal) in fasting and post-stimulation tests increase ≥ 100%

  6. Participant has not yet been diagnosed with stage 2 or 3 type 1 diabetes mellitus (no history of dysglycemia, no history of clinical symptoms of type 1 diabetes mellitus)

  7. HbA1c level (%) <5,7% (acc. to ADA)

  8. Positive autoantibody titres (ICA, IAA, GAD, IA-2/ICA512, ZnT8) - low titers of two or more antibodies (2-4 times the normal*); if high titer of one of the antibodies (≥ 4 times the norm, not applicable to ICA) re-screening allowed (the participant can be included in the trial only after confirming two or more antibodies)

  9. Ability to give informed consent by the child's legal representatives (and the child himself or herself if he or she is over the age of 13 at the time of the trial [according to local law])

  10. Ability of the child's legal representatives to manage diabetes, defined as blood glucose levels control at least three times a day and the ability to dose insulin correctly.

  11. Venous access to guarantee blood donation

    Exclusion Criteria:

  12. Refusal to participate in the trial or lack of a signed informed consent form

  13. Suspicion or diagnosis for a type of diabetes other than type 1 diabetes mellitus

  14. Age under 6 or above 16

  15. IgA deficiency or history of other diagnosed immunodeficiency (max. 7 infections/year allowed, and the prognosis should indicate that the patient will remain in the study throughout its duration)

  16. C-peptide levels < 1.0 ng/ml fasting and in post-stimulation tests increase < 100%

  17. Glucose levels in venous blood ≥ 100mg% fasting

  18. Glucose levels in venous blood after 1 and 2 hours in OGTT ≥ 200mg%

  19. Glycated hemoglobin level (HbA1c) in venous blood ≥ 5,7%

  20. BMI < 25 or > 75th percentile for a given age or weight of less than 20 kg

  21. History of hypersensitivity to anti-CD20 or other components of the preparation

  22. History of hypersensitivity to penicillin and/or streptomycin

  23. Past or active infection with HBV, HCV, HIV, HTLV I/II, mycobacterium tuberculosis, syphilis. Laboratory evidence of infection without the need for clinical signs and symptoms is sufficient for diagnosis.

  24. Active infection with the EBV or CMV virus (positive IgM)

  25. Any fungal, parasitic, viral, or bacterial infection

  26. History of past or active cancer

  27. Anemia, lymphopenia, neutropenia, or thrombocytopenia defined as a blood cell count below the lower limit of normal for age found within the last 6 weeks prior to trial inclusion

  28. Elevated thrombotic activity/history of thrombosis episode

  29. Any disease prior to inclusion in the trial currently requiring medication for more than 3 months in history

  30. Diagnosed autoimmune disease other than type 1 diabetes mellitus, including a history of Hashimoto's disease and coeliac disease

  31. Taking anti-diabetic medication (including insulin) in the last 4 weeks prior to trial inclusion

  32. History of retinopathy

  33. History of hypertension

  34. Current or history of albuminuria

  35. For women in childbearing potential/menstruating women: pregnancy (from medical interview) or unwillingness to exercise sexual restraint or use effective forms of contraception for the duration of the trial and up to 4 months after completion, if applicable.

    The following contraceptive methods are acceptable: bilateral fallopian tube closure, sterilization in men, appropriate use of hormonal contraception that inhibits ovulation, hormone-releasing IUDs, and copper IUDs, male or female condoms with spermicide; and cap, uterine disc, or sponge with spermicide.

  36. Breastfeeding

  37. For males over 15 years of age: expressed intention to have offspring or donate sperm during the trial or within 4 months after the end of the trial, if applicable

  38. Excessive anxiety of the participant or his/her legal representatives regarding the procedures used in the trial

  39. Any medical problem that, in the opinion of the investigator, may adversely affect the participant's health if included in the trial

  40. Legal representatives and/or children over the age of 15 with an identified alcohol and/or psychoactive substance addiction

  41. History of disease of unknown etiology

  42. History of Creutzfeldt-Jacob disease

  43. History of progressive dementia or degenerative neurological disease, including of unknown origin

  44. History of taking hormones derived from the human pituitary gland (e.g., growth hormone)

  45. Treatment with immunosuppressants

  46. History of corneal, scleral, and dural transplant or undocumented neurosurgery

  47. History of occurrence of risk factors related to the participant's travel, where there is a possibility of exposure to regional infectious diseases

  48. Physical signs that indicate the risk of an infectious disease

  49. History of xenogeneic transplant

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

150 participants in 4 patient groups, including a placebo group

TregsCD20
Experimental group
Description:
Infusion of Treg preparation at "day 0" + 4 doses of antiCD20 antibody; second infusion of Treg preparation at time "+90±30days" Interventions: ex vivo expanded CD4+CD25+CD127- regulatory T cells (Tregs) + Anti-CD20 (rituximab)
Tregs only
Experimental group
Description:
Infusion of Treg preparation at "day 0" + 4 doses of placebo; second infusion of Treg preparation at time "+90±30 days"
Treatment:
Biological: ex vivo expanded CD4+CD25+CD127- regulatory T cells (Tregs)
Other: Placebo
CD20 only
Experimental group
Description:
Infusion of Treg sham at "day 0" + 4 doses of antiCD20 antibody; second infusion of Treg sham at time "+90±30days"
Treatment:
Other: Treg sham
Biological: Anti-CD20 (rituximab)
Control group
Placebo Comparator group
Description:
Infusion of Treg sham at "day 0" + 4 doses of placebo; second infusion of Treg sham at time "+90±30days"
Treatment:
Other: Treg sham
Other: Placebo

Trial contacts and locations

8

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Central trial contact

Grzegorz Orlik, Medical Director; Marta Druch, Clinical Trial Director

Data sourced from clinicaltrials.gov

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