Status:

UNKNOWN

Quality of Life Improvements With Cord Blood Plasma

Lead Sponsor:

Hexagon Therapies, LLC

Conditions:

Aging

Eligibility:

All Genders

50-80 years

Phase:

PHASE1

Brief Summary

This study aims to look at whether human umbilical cord blood plasma (HUCBP) is safe for intravascular (iv) administration; and whether it provides any reversal of frailty or other age-related biologi...

Detailed Description

Participants that take part in this experimental treatment will receive six HUCBP infusions over a six month period, with a final check-up occuring six months after the last infusion. Blood samples wi...

Eligibility Criteria

Inclusion

  • Aged 50 or older
  • Be willing and able to participate during the 12 month research period
  • Women - must be diagnosed with infertility or menopause

Exclusion

  • Unable to perform tasks required for analysis of end points
  • History of being hospitalized dues to infectious disease, such as pneumonia, within the last year
  • Recent and current use of immunosuppressive drugs or HIV patients
  • Scheduled to receive organ transplant
  • Dementia or clinically relevant cognitive impairment
  • Participants of previous (within 1 month) or current clinical trials
  • Severe heart and kidney failure
  • History of alcohol or drug abuse
  • Known or suspected pregnancy
  • Chronic Hepatitis B or C
  • Diagnosis of cancer within 5 year of the study, or the possibility to contract cancer
  • Anticancer chemotherapy and radiation therapy

Key Trial Info

Start Date :

April 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 1 2019

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT03229785

Start Date

April 1 2018

End Date

August 1 2019

Last Update

January 24 2018

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