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Erectile DysfunctionPhase 1NCT05147779

Safety of Cultured Allogeneic Adult Umbilical Cord Stem Cells for Peyronie's Disease, ED, and Interstitial Cystitis

A Phase 1 study testing AlloRx in people with Erectile Dysfunction and Peyronie's Disease, run by The Foundation for Orthopaedics and Regenerative Medicine at 1 site in Antigua and Barbuda.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record

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Trial summary

This trial will study the safety and efficacy of intravenous and intracavernosal or interstitial delivery of cultured allogeneic adult umbilical cord derived mesenchymal stem cells for the treatment of Peyronie's disease, erectile dysfunction , and Interstitial Cystitis Read more about this study

Who is it for?
Any age
What is being tested?
AlloRx
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteAntigua and Barbuda
Study dates
12 Sep 2021to 30 Dec 2025
Phase
Phase 1

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Diagnosis of Peyronie's Disease, erectile dysfunction, or Interstitial Cystitis
  • Understanding and willingness to sign a written informed consent document

Who cannot join

  • Active infection
  • Active cancer
  • Chronic multisystem organ failure
  • Pregnancy
  • Clinically significant Abnormalities on pre-treatment laboratory evaluation
  • Medical condition that would (based on the opinion of the investigator) compromise patient's safety.
Show all 10Show fewer
  • Continued drug abuse
  • Pre-menopausal women not using contraception
  • Previous organ transplant
  • Hypersensitivity to sulfur

Trial locations and contacts

1 site in 1 country.

Antigua and Barbuda1 site
  • Medical Surgical Associates Center

    St John's

About this study

Official title: Safety of Cultured Allogeneic Adult Umbilical Cord Derived Mesenchymal Stem Cells for the Treatment of Peyronie's Disease, Erectile Dysfunction, and Interstitial Cystitis

This trial will study the safety and efficacy of intravenous and intracavernosal or interstitial delivery of cultured allogeneic adult umbilical cord derived mesenchymal stem cells for the treatment of Peyronie's disease, erectile dysfunction , and Interstitial Cystitis

Read the detailed description

This patient funded trial aims to study the safety and efficacy of intravenous and intracavernosal or interstitial delivery of cultured allogeneic adult umbilical cord derived mesenchymal stem cells (UC-MSCs) for the treatment of Peyronie's disease, erectile dysfunction , and Interstitial Cystitis. The total dose will be 100 million cells. Patients will be evaluated within one month pre treatment and at 1, 6, 12, 24, 36, and 48 months post treatment for safety and efficacy.

Being tested
AlloRx
Keywords
Erectile Dysfunction, Peyronie's Disease, stem cell treatment, Interstitial Cystitis
Medical subject headings
Erectile Dysfunction, Penile Induration, Cystitis, Interstitial

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AlloRxBiological

    cultured allogeneic adult umbilical cord derived mesenchymal stem cells

Study groups in NCT05147779
Study groupRoleWhat they receive
Treatment Group (AlloRx)Experimentalintravenous and intracavernosal or interstitial delivery (total dose of 100 million cells)
Receives: Biological: AlloRx

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Safety (adverse events)

    Clinical monitoring of possible adverse events or complications

    Measured: Four year follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Dec 2021
  2. Study start12 Sep 2021
  3. Primary completion30 Dec 2025
  4. Study completion30 Dec 2025

Why it stopped: Inadequate treatment response observed in preliminary data did not justify enrolling further study participants

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05147779
Sponsor's protocol ID
ATG-1-MSC-015
Status last verified
Oct 2026
First submitted
29 Nov 2021
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Publications

  • Al Demour S, Jafar H, Adwan S, AlSharif A, Alhawari H, Alrabadi A, Zayed A, Jaradat A, Awidi A. Safety and Potential Therapeutic Effect of Two Intracavernous Autologous Bone Marrow Derived Mesenchymal Stem Cells injections in Diabetic Patients with Erectile Dysfunction: An Open Label Phase I Clinical Trial. Urol Int. 2018;101(3):358-365. doi: 10.1159/000492120. Epub 2018 Aug 31.

    PubMed 30173210
  • Bahk JY, Jung JH, Han H, Min SK, Lee YS. Treatment of diabetic impotence with umbilical cord blood stem cell intracavernosal transplant: preliminary report of 7 cases. Exp Clin Transplant. 2010 Jun;8(2):150-60.

    PubMed 20565373
  • Levy JA, Marchand M, Iorio L, Zribi G, Zahalsky MP. Effects of Stem Cell Treatment in Human Patients With Peyronie Disease. J Am Osteopath Assoc. 2015 Oct;115(10):e8-13. doi: 10.7556/jaoa.2015.124.

    PubMed 26414724

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