Mesenchymal Stromal Cells to Treat Type 1 Diabetes in Children and Adolescents

Launched by UPPSALA UNIVERSITY HOSPITAL · Sep 20, 2021

Keywords

ClinConnect Summary

This clinical trial is investigating the use of special cells called mesenchymal stromal cells to see if they can help treat type 1 diabetes in children and teenagers aged 7 to 21 who have been diagnosed with the condition within the last six months. The study has two parts: the first part will involve a small group of six participants who will receive these cells, while the second part will include 60 more participants who will be randomly assigned to receive either the cell treatment or a placebo (a fake treatment) for comparison. The main goals of the study are to check how safe the treatment is and whether it can effectively help manage type 1 diabetes.

To be eligible for this trial, participants need to be between 7 and 21 years old, have a recent diagnosis of type 1 diabetes, and be mentally stable enough to follow the study’s guidelines. They must also have a certain level of a specific protein in their blood called C-peptide. Importantly, they should not have certain health issues, such as unstable heart conditions or active infections. Those who join the study can expect to receive close monitoring during and after the treatment to ensure their safety and assess the effectiveness of the cells. This trial is currently recruiting participants, and caregivers' consent is required for those under 18 years old.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Written informed consent for participation of the study (for subjects below 18 years of age also from both caregivers), given before undergoing any study-specific procedures
• • 2. Clinical history compatible with type 1 diabetes diagnosed less than 6 months before enrolment
• • 3. In the first part of the study, six subjects, three between 7-11 and three between 12-18 years of age (both groups inclusive at both ends), will be included. The sixty subjects in the second part of the study are stratified by age (12-21 and 7-11 years, respectively) and randomized to one of two treatment arms (active or placebo), with a 6-month safety delay for the younger stratum.
• • 4. Mentally stable and, in the opinion of the investigator, able to comply with the procedures of the study protocol.
• • 5. Fasting plasma C-peptide concentration \>0.12 nmol/L.
• 6. Subjects of child-bearing potential must agree to using adequate contraception until one year after the administration of WJMSC/Placebo. Adequate contraception is as follows:
• • 1. oral (except low-dose gestagen (lynestrenol and noretisteron), injectable or implanted hormonal contraceptives.
• • 2. intrauterine device
• • 3. intrauterine system (for example progestin-releasing coil)
• • 4. vasectomized male (with appropriate postvasectomy documentation of the absence of sperm in the ejaculate)
• Exclusion Criteria:
• • 1. Subjects with body weight \>100 kg
• • 2. Subjects with unstable cardiovascular status incl. NYHA class III/IV or symptoms of angina pectoris.
• • 3. Subjects with uncontrolled hypertension (≥160/105 mmHg).
• • 4. Subjects with active on-going infections.
• • 5. Subjects with latent or previous as well as on-going therapy against tuberculosis, or exposed to tuberculosis or has traveled in areas with a high risk of tuberculosis or mycosis within the last 3 months.
• • 6. Subjects with serological evidence of infection with HIV, Treponema pallidum, hepatitis B antigen (subjects with serology consistent with previous vaccination and a history of vaccination are acceptable), or hepatitis C.
• • 7. Subjects with any systemic immune suppressive treatment
• • 8. Subjects with a known demyelinating disease or with symptoms or physical examination findings consistent with possible demyelinating disease.
• • 9. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test.
• • 10. Subjects with known, or previous, malignancy.
• • 11. Taking oral anti-diabetic therapies or any other concomitant medication which may interfere with glucose regulation other than insulin.
• • 12. Subjects with GFR \<60 ml/min/1.73 m2 body surface.
• • 13. Subject with any condition or any circumstance that, in the opinion of the investigator, would make it unsafe to undergo treatment with MSC.
• • 14. Known hypersensitivity against any excipients, i.e., dimethyl sulfoxide (DMSO).