Reversing Epigenetic & Other Markers of Senescence by Transfusing Young Plasma To Older Human Subjects

Status unconfirmed · Phase 1/Phase 2

Conditions studied: Aging

In brief

This trial is designed to study the effects of monthly transfusions of young healthy male donor plasma on biological age as assessed by DNA methylation levels, and changes in cognitive, renal, and pulmonary function, muscle strength, telomere length, testosterone, estrogen, DHEAS, IGF-1, high resolution C-Reactive protein, and expression of P16INK4a in peripheral blood T lymphocytes and skin biopsies.

Key facts

Study ID

NCT03353597

Run by

Chandra Duggirala

People needed

2120

Starts

2018-05-15

Expected to finish

2022-12-15

Last updated by the study team

2018-01-17

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Age > 40.
• Stable medications for 2 months prior to Screening.
• Signed and dated written informed consent obtained from the subject in accordance with local Institutional Review Board regulations.
• Males and all Women of Child Bearing Potential agree to abstain from sex or use an adequate method of contraception for the duration of the study and for 30 days after the last dose of study drug. Adequate contraceptive methods include those with a low failure rate, i.e., less than 1% per year, when used consistently and correctly), and , a woman who has been surgically sterilized or who has been in a state of amenorrhea.

You may not qualify if…

• Dementia of any etiology.
• Any medical condition other than dementia that could account for cognitive deficits (e.g., active seizure disorder, stroke, Central Nervous System diseases);
• History of significant cardiovascular, hematologic, renal, or advanced hepatic disease (or laboratory evidence thereof);
• History of major psychiatric illness or untreated depression;
• Neutrophil count <1,500/mm3, platelets <100,000/mm3, serum creatinine >1.5x upper limit of normal (ULN), total bilirubin >1.5 x ULN, Alanine Transaminase >3 x ULN, Aspartate Transaminase >3 x ULN, or International Normalized Ratio (INR) >1.2 at Screening evaluations;
• Evidence of any clinically significant findings on Screening or baseline evaluations which, in the opinion of the Investigator would pose a safety risk or interfere with appropriate interpretation of study data;
• Current or recent history (within four weeks prior to Screening) of a clinically significant bacterial, fungal, or mycobacterial infection;
• Current clinically significant viral infection;
• Major surgery within four weeks prior to Screening;
• Any contraindication to monthly plasma transfusions, including but not limited to:
• History of significant transfusion complications;
• Compatible plasma units not available;
• Prior intolerance to intravenous (IV) fluids;
• Immunoglobulin A deficiency by history or laboratory evidence at Screening;
• Bleeding;
• Any concurrent use of an anti-coagulant therapy.
• Daily administration of Aspirin 81mg will be allowed as long as the dose is stable for 30 days prior to Screening. Anti-platelet drugs are acceptable.
• Treatment with another investigational drug or participation in another interventional clinical trial within 3 months of Screening;
• Treatment with any human blood product, including IV immunoglobulin, during the 6 months prior to Screening or during the trial;
• Pregnant or lactating;
• Positive pregnancy test at Screening or Baseline (Day 1);
• Cancer within 5 years of Screening, except for nonmetastatic skin cancer or non-metastatic prostate cancer not expected to cause significant morbidity or mortality within one year of Baseline.
• AB blood type.

Where it is running

• The Infusion Center & Clinic — San Mateo, California, United States

Full record on ClinicalTrials.gov

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