Recruiting
Phase 1

AdiaVita & Glutathione

Sponsor:

Adia Med of Winter Park LLC

Code:

NCT07572890

Conditions

Chronic Kidney Disease

Kidney Disease

Kidney Disease, Chronic

Chronic Kidney Disease (CKD)

CKD

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Umbilical Cord Blood-Derived Stem Cells and Exosomes

Glutathione IV

Glutathione Spray

Placebo IV

Placebo Glutathione IV

Study Details

Brief summary:

The goal of this clinical trial is to learn whether a new regenerative treatment called AdiaVita, made from umbilical cord blood-derived stem cells and exosomes combined with glutathione, is safe and can help improve kidney function in adults with chronic kidney disease (CKD). In this condition, the kidneys gradually lose their ability to filter blood as well as they should. The main questions it aims to answer are whether AdiaVita plus glutathione improves kidney function better than control treatments, as measured by blood tests for estimated glomerular filtration rate (eGFR) and creatinine levels, and whether the treatment is safe with acceptable side effects. Researchers will compare three groups. One group will receive AdiaVita plus glutathione. A second group will receive glutathione plus a placebo for AdiaVita. The third group will receive placebos for both treatments. A placebo looks like the real treatment but contains no active ingredients. This will help determine if the full treatment works better than the controls. Approximately 100 adults aged 18 to 80 with stage 2 to 4 chronic kidney disease may participate. Participants will be randomly assigned to one of the three treatment groups. They will receive monthly intravenous infusions at the clinic for the first three months and apply a skin spray twice daily at home during that period. The study lasts 12 months total for each participant, with regular visits for blood tests, physical exams, and safety monitoring. Certain participants in the control groups may switch to the active AdiaVita treatment after three months if they meet safety criteria. This is a single-blind study, meaning participants will not know which treatment they receive. Participant safety is closely monitored by the research team and an independent board throughout the study.

Conditions

Chronic Kidney Disease

Kidney Disease

Kidney Disease, Chronic

Chronic Kidney Disease (CKD)

CKD

Study ID

NCT07572890

Start date

May 18, 2026

Status verified date

Jun, 2026

Completion date

Jan, 2029

Anticipated

Primary completion date

Jan, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age 18-80 years
  • Confirmed CKD diagnosis (eGFR 15-89 mL/min/1.73 m²)
  • Willingness to consider experimental treatments and comply with study requirements
  • Ability to obtain required bloodwork
  • Ability to attend all scheduled visits
  • Able to meet study cost requirements ($15,000 study fee) as described in the informed consent

Exclusion Criteria:

  • Has
  • Severe allergies to study products
  • Significant uncontrolled medical conditions
  • Immunocompromised
  • Malignancy history
  • Unstable medication regimen or inconsistent medication adherence (e.g., frequent medication changes or missed doses) within 30 days prior to Baseline, at Investigator discretion
  • Current dialysis (hemodialysis or peritoneal dialysis) or planned initiation of dialysis during the study period
  • Pregnancy or breastfeeding (if applicable)
  • Participation in another interventional trial within 30 days
  • Has had Kidney transplant
  • Prior stem cell or glutathione therapy: History of stem cell therapy (including umbilical cord blood-derived stem cells or exosomes) or glutathione therapy (intravenous or topical) at any time prior to screening

Study Design

Enrollment

100 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Stem Cell + Glutathione

active comparator: Glutathione Control (with Crossover)

placebo comparator: Placebo Control (with Crossover)

Interventions

Umbilical Cord Blood-Derived Stem Cells and Exosomes

Intravenous infusion of cryopreserved allogeneic umbilical cord blood-derived product containing viable mononuclear cells (including hematopoietic and mesenchymal stem/stromal cells) and exosomes.

Glutathione IV

Reduced L-glutathione administered Intravenous infusion once monthly for 3 months (Initial Treatment Schedule)

Glutathione Spray

Transdermal glutathione spray (4 sprays applied twice daily to the skin).

Placebo IV

Matched placebo intravenous infusion (administered in the same volume and manner as stem cell and exosome product).

Placebo Glutathione IV

Matched placebo intravenous infusion administered on the same schedule as active glutathione IV.

Placebo Spray

Matched placebo transdermal spray (4 sprays applied twice daily).

Primary outcome measure

  • Change from Baseline in Estimated Glomerular Filtration Rate (eGFR) [ Time Frame: Baseline to Month 6 ]
  • Change from Baseline in Serum Creatinine [ Time Frame: Baseline to Month 6 ]

Central Contacts and Locations

Central contacts

Locations

Adia Med Of Winter Park

Recruiting

Winter Park, Florida, United States, 32789

Contacts

More Information

Sponsor

Adia Med of Winter Park LLC

Last update posted

Jun 17, 2026

Last verified

Jun, 2026

Keywords

  • allogeneic stem cells
  • antioxidant therapy
  • stem cell therapy
  • stem cells
  • Chronic Kidney Disease
  • CKD
  • Regenerative medicine
  • Glutathione
  • Glutathione therapy

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Adia Med of Winter Park LLC on 2026-06-17.