Expanded Access Use of Human Umbilical Cord Blood (REGENECYTE) Infusion in Patients With Chronic Fatigue of Post-COVID Condition

Trial statusAvailable
Trial phaseNot listed
Trial typeExpanded Access
Biological sexAll
Age18+
SponsorStemCyte, Inc.

About this trial

REGENECYTE® (HPC, Cord Blood (Hematopoietic Progenitor Cell, Cord Blood)) for treatment in patients with post-COVID.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female aged ≥ 18

With post-COVID condition

Has had a recent (within 7 days) negative SARS-CoV-2 test (an approved PCR (polyermerase chain reaction) or antigen test)

Not eligible for participation in any ongoing clinical trials of post-COVID condition with REGENECYTE

Disqualifiers

Neurological disorders prior to COVID-19 diagnosis

With pre-existing terminal illness

With known immune disease

Is pregnant or breastfeeding

Trial design

Treatments tested in this trial

  • REGENECYTE®

    Biological/Vaccine

    HPC, Cord Blood (Hematopoietic Progenitor Cell, Cord Blood)

Treatment groups

No treatment groups listed

Trial outcomes

This trial has no outcomes listed.

Sponsors and contacts

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