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Stem Cell Therapy
Fat-Derived Stem Cell Therapy for Inflammatory Bowel Disease (ADcSVF-IBD Trial)
Phase 1 & 2
Waitlist Available
Led By Robert W Alexander, MD
Research Sponsored by Healeon Medical Inc
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Negative pregnancy test for women of childbearing age (menarche to menopause)
Be older than 18 years old
Must not have
Patients with history of colectomy
Severe IBD preventing tolerance of procedures needed
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month, 6 month, 1 year
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new treatment using special cells taken from a patient's own fat tissue. These cells are used to help reduce inflammation and promote healing in patients with Inflammatory Bowel Disease (IBD), including Ulcerative Colitis and Crohn's Disease. The goal is to find a more effective treatment that addresses the root causes of the disease rather than just the symptoms.
Who is the study for?
This trial is for individuals with Inflammatory Bowel Disease diagnosed at least 6 months ago. It's open to adults and minors under 18 with guardian approval. Participants must be able to consent, not pregnant, and without severe IBD that prevents procedure tolerance or requires immediate steroids or surgery.
What is being tested?
The study tests the use of one's own fat-derived stem cells (AD-cSVF) against IBD symptoms compared to a saline solution control group. The process includes lipoaspiration (fat removal) and then administering these cells intravenously.
What are the potential side effects?
Potential side effects may include discomfort from lipoaspiration, typical risks associated with IV treatments like infection or inflammation at the injection site, and any unknown reactions related to stem cell therapy.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am not pregnant.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had surgery to remove part or all of my colon.
Select...
My severe IBD prevents me from tolerating certain medical procedures.
Select...
I am currently taking corticosteroids and need them to manage my condition.
Select...
I am able to understand and consent to the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 month, 6 month, 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 month, 6 month, 1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety: Inflammatory Bowel Disease
Secondary study objectives
Change from Baseline in C Reactive Protein (CRP)
Efficacy: Change in Baseline in Lichtiger Index
Efficacy: Change in Baseline of Modified Truelove-Witts Score (MTW)
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: Normal Saline IV Arm 3Experimental Treatment1 Intervention
Normal Saline IV with AD-cSVF cells
Group II: Lipoaspiration Arm 1Experimental Treatment1 Intervention
Acquisition of Adipose-Derived tissue Stromal Vascular Fraction (AD-tSVF) via closed syringe harvest subdermal fat
Group III: AD-cSVF Arm 2Experimental Treatment1 Intervention
Isolation of cellular stem/stromal cells from subdermal adipose-derived cellular stromal vascular fraction (AD-cSVF)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lipoaspiration
2022
Completed Phase 2
~20
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Inflammatory Bowel Disease (IBD) such as mesalamine, glucocorticoids, and biologic agents like infliximab and adalimumab primarily work by modulating the immune response, reducing inflammation, and promoting tissue repair. Mesalamine acts locally in the gut to reduce inflammation, while glucocorticoids suppress the overall immune response to decrease inflammation.
Biologic agents target specific components of the immune system, such as tumor necrosis factor (TNF), to prevent inflammatory processes. Treatments like Adipose-Derived Stem/Stromal Cells (AD-cSVF) are being studied for their potential to modulate immune responses, promote tissue repair, and reduce inflammation, which could offer a more targeted and regenerative approach to managing IBD.
These mechanisms are crucial for IBD patients as they aim to control chronic inflammation, promote healing of the intestinal lining, and improve overall quality of life.
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Who is running the clinical trial?
Healeon Medical IncLead Sponsor
8 Previous Clinical Trials
610 Total Patients Enrolled
Terry, Glenn C., M.D.INDIV
4 Previous Clinical Trials
360 Total Patients Enrolled
Robert W Alexander, MDPrincipal InvestigatorHealeon Medical Inc
6 Previous Clinical Trials
770 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I need immediate treatment for my condition, as judged by my doctor.I have had surgery to remove part or all of my colon.I am under 18 and have consent from my guardians and the study's investigators.I am not pregnant.I was diagnosed with IBD at least 6 months ago.I haven't been in a drug trial or had cancer treatment in the last 6 months.I am 18 or older and have been diagnosed with IBD.My severe IBD prevents me from tolerating certain medical procedures.I am currently taking corticosteroids and need them to manage my condition.I am able to understand and consent to the study.
Research Study Groups:
This trial has the following groups:- Group 1: Lipoaspiration Arm 1
- Group 2: AD-cSVF Arm 2
- Group 3: Normal Saline IV Arm 3
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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