Join a Journey that Brings New Hope
to No-Option Patients

BioGenCell’s Phase 2 Clinical Trial for BGC 101
Double blind randomized placebo controlled study to assess the feasibility of BGC101(EnEPC) in treating Critical Limb Ischemia.

If you are a Physician, you can contact us for more information or refer patients

If you are a patient, a patient’s family member, or an interested party

Quick Overview

We’re Actively Recruiting

Age & Gender

Conditions

Testing

Principal Investigators (PIs)

Inclusion and
Exclusion Criteria

Inclusions

Exclusions (partial list)

HealthCare Providers
Learn About the Benefits of BioGenCell

Get in touch with us to learn about the value of our treatments for clinicians and healthcare providers

biogencell trial

Accessible

biogencell trial

Clinician-Friendly

biogencell trial

Easy to Use

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Rapid

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Lasting Effect

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Safe

FAQ
For Healthcare Providers

The purpose of this clinical trial is to evaluate the efficacy and safety of our innovative cell-therapy solution for patients with critical limb ischemia (CLI) and chronic limb-threatening ischemia (CLTI), with the end goal being 12 months amputation-free survival.
BGC101 phase 2 clinical trial is considered for the FDA’s fast track, and therefore requires xxx patients to be enrolled.

Patients over 18 years old, of all genders, suffering from No-Option Chronic Limb Threatening Ischemia, Rutherford 4-5, with Severe Arterial Occlusive Peripheral Disease and not amenable for further revascularization.

If you’re interested in participating in this clinical trial, speak to your doctor or contact the trial coordinators for more information on how to apply.
The three steps of the cell-therapy solution include a simple blood draw, a rapid processing stage in which the patient’s own stem cells are re-trained by the immune system cells – and shortly after administered directly to the patient via injection.
The treatment process will involve only two visits to the clinic- one for the simple blood draw and one shortly after, for the rapid and simple re-injection of the “re-trained” blood cells.
The potential benefits of this cell-therapy solution include improved blood flow to the affected limb, reduced pain, increased mobility, and an overall better quality of life for patients with CLI and CLTI.
Like all clinical trials, this study comes with risks, such as the risk of infection or injury from the blood draw or injection sites. Your doctor will inform you of all the potential risk before enrolling in the study.
Once the study is over, research data is analyzed to assess the safety and efficacy of the cell-therapy solution. The results of the study may inform whether or not the cell-therapy solution becomes available to patients as an accessible and approved treatment.
Yes, you can withdraw from the clinical trial at any point without any obligation or impact on your medical care. Your doctor will discuss options before you make the decision to withdraw.

Patients and Their Families
Learn More About BioGenCell

biogencell trial

Personalized

biogencell trial

3 Simple Steps

biogencell trial

Patient Friendly

biogencell trial

Safe

biogencell trial

Lasting Effect

biogencell trial

Accessible

FAQ
Patients and Their Families

The purpose of this clinical trial is to evaluate the efficacy and safety of our innovative cell-therapy solution for patients with critical limb ischemia (CLI) and chronic limb-threatening ischemia (CLTI), with the end goal being 12 months amputation-free survival.
BGC101 phase 2 clinical trial is considered for the FDA’s fast track, and therefore requires xxx patients to be enrolled.

Patients over 18 years old, of all genders, suffering from No-Option Chronic Limb Threatening Ischemia, Rutherford 4-5, with Severe Arterial Occlusive Peripheral Disease and not amenable for further revascularization.

If you’re interested in participating in this clinical trial, speak to your doctor or contact the trial coordinators for more information on how to apply.
The three steps of the cell-therapy solution include a simple blood draw, a rapid processing stage in which the patient’s own stem cells are re-trained by the immune system cells – and shortly after administered directly to the patient via injection.
The treatment process will involve only two visits to the clinic- one for the simple blood draw and one shortly after, for the rapid and simple re-injection of the “re-trained” blood cells.
The potential benefits of this cell-therapy solution include improved blood flow to the affected limb, reduced pain, increased mobility, and an overall better quality of life for patients with CLI and CLTI.
Like all clinical trials, this study comes with risks, such as the risk of infection or injury from the blood draw or injection sites. Your doctor will inform you of all the potential risk before enrolling in the study.
Once the study is over, research data is analyzed to assess the safety and efficacy of the cell-therapy solution. The results of the study may inform whether or not the cell-therapy solution becomes available to patients as an accessible and approved treatment.
Yes, you can withdraw from the clinical trial at any point without any obligation or impact on your medical care. Your doctor will discuss options before you make the decision to withdraw.

The Science: Hind-Limb Ischemia as a Model
for Vascular Diseases and CLI

Incorporation in the tissue, increased capillary density & perfusion are concentrated in and restricted to the injured area to provide maximal benefit without untoward effects.

Study Design

study

Safety

safety

Mode of Action

mode-of-action

Efficacy

efficacy
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