Safety of Cultured Allogeneic Adult Umbilical Cord Derived Mesenchymal Stem Cells for NAION

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorThe Foundation for Orthopaedics and Regenerative Medicine

About this trial

This trial will study the safety and efficacy of intravenous and sub-tenon delivery of cultured allogeneic adult umbilical cord derived mesenchymal stem cells for the treatment of non-arteritic ischemic optic neuropathy

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of NAION (non-arteritic ischemic optic neuropathy)

Understanding and willingness to sign a written informed consent document

Disqualifiers

Active infection

Active cancer

Chronic multisystem organ failure

Pregnancy

Trial design

Design model

Single group

Treatments tested in this trial

  • AlloRx

    Biological/Vaccine

    cultured allogeneic adult umbilical cord derived mesenchymal stem cells

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Treatment Group (AlloRx)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Safety (adverse events)

Clinical monitoring of possible adverse events or complications

Time frame
Four year follow-up

Secondary outcomes

Other outcomes

Sponsors and contacts

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