Use of Autologous, Adult Adipose-Derived Stem/Stromal Cells in Inflammatory Bowel Disease (ADcSVF-IBD)
Primary Purpose
Inflammatory Bowel Diseases
Status
Enrolling by invitation
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Lipoaspiration
AD-cSVF
Normal Saline IV
Sponsored by
About this trial
This is an interventional treatment trial for Inflammatory Bowel Diseases focused on measuring IBD,Crohn's,Ulcerative Bowel; Diverticulitis;IBS;UC
Eligibility Criteria
Inclusion Criteria:
- Patients, either sex 18 years and older with confirmed diagnosis of IBD
- Patients, either sex younger than 18 years upon approval of responsible parties and agreement of investigators
- Ability of patient to provide informed consent (or legal guardian)
- IBD diagnosed at least 6 months earlier to therapy using usual criteria
- Negative pregnancy test for women of childbearing age (menarche to menopause)
Exclusion Criteria:
- Mental incapacity that prevents adequate understanding of study and associate procedures and providing informed consent
- Severe IBD preventing tolerance of procedures needed
- Patients with impaired systemic condition, according to investigator judgment, needs immediate corticosteroid or surgical intervention
- Patients that fulfill criteria of cortico-dependency and in current treatment with corticosteroids
- Patients with history of colectomy
- Known history of alcohol, smoking dependence or additive substance abuse
- History related malignant disease - including patients participating in clinical trial with investigational drug within 6 months
- Patients with known history of allergies to any substance used in this protocol
- Pregnant or breastfeeding females
- Presence of severe concomitant disease, in investigators opinion threatens patient's well being or safety
Sites / Locations
- Regenevita LLC
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
Lipoaspiration Arm 1
AD-cSVF Arm 2
Normal Saline IV Arm 3
Arm Description
Acquisition of Adipose-Derived tissue Stromal Vascular Fraction (AD-tSVF) via closed syringe harvest subdermal fat
Isolation of cellular stem/stromal cells from subdermal adipose-derived cellular stromal vascular fraction (AD-cSVF)
Normal Saline IV with AD-cSVF cells
Outcomes
Primary Outcome Measures
Safety: Inflammatory Bowel Disease
Inflammatory Bowel Disease to be addressed as occurrence or frequency of adverse event during study. Includes vital signs, complete blood count, and disease progression
Secondary Outcome Measures
Efficacy: Quality of life index , Inflammatory Bowel Disease Questionnaire(IBD-QoL)
Comparison of response if it improves at least 30%
Change from Baseline in C Reactive Protein (CRP)
Blood draw and laboratory measure of CRP as reflection of inflammatory baseline change
Efficacy: Change in Baseline of Modified Truelove-Witts Score (MTW)
Remission is considered if below 11, and response if it diminishes at least 30%
Efficacy: Change in Baseline in Lichtiger Index
Remission considered if reaching 0 point, and response if the score diminishes from pretreatment level
Full Information
NCT ID
NCT02952131
First Posted
October 30, 2016
Last Updated
August 1, 2022
Sponsor
Healeon Medical Inc
Collaborators
Terry, Glenn C., M.D.
1. Study Identification
Unique Protocol Identification Number
NCT02952131
Brief Title
Use of Autologous, Adult Adipose-Derived Stem/Stromal Cells in Inflammatory Bowel Disease
Acronym
ADcSVF-IBD
Official Title
Use of Autologous Adult Adipose-Derived Stem/Stromal Cells in Inflammatory Bowel Disease
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
November 2016 (undefined)
Primary Completion Date
August 14, 2024 (Anticipated)
Study Completion Date
June 19, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Healeon Medical Inc
Collaborators
Terry, Glenn C., M.D.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Inflammatory Bowel Disease (IBD) is a group of inflammatory conditions of the small bowel and colon. Main types include Ulcerative Colitis and Crohn's Disease. Symptoms are often difficult to distinguish except for location and nature of changes. IBD complex arises with interaction of environmental, genetic factors, immunological responses, and chronic and recurring inflammation.
Many factor appear as contributory, but no single set of issues appear to explain the process. Microbiota, intestinal wall granulation or breach, dietary, genetic predisposition all appear to factors. Treatment is often reactive or suppressive medications, neither of which appears to reverse the disease processes. This study explores the value of a complex group of adipose-derived stem/stromal cells (AD-cSVF) in the disease process.
Detailed Description
IBD often presents clinically as abdominal pain, diarrhea (with and without blood), fever, weight loss, failure to thrive, and many related symptoms. Complications of the disorders may also include anemia, skin rashes, arthritis, severe chronic fatigue, and eye inflammatory changes.
It is felt that IBD disorders may be caused by combination of environmental, immune, genetic, and bacterial factors. Results of these issues produce a chronic inflammatory disorder, in which the immune system attacks the gastrointestinal tract, perhaps directed by certain microbial antigens. The group appears not to be a pure autoimmune disease reaction, but may relate to a immunodeficiency state.
There are no medications or surgical procedures that are known to cure the diseases. Most are aimed at reduction of symptoms, maintain remissions, and try to prevent relapses. Temporary anti-inflammatory medications may improve the acute process, followed by methotrexate or thiopurine to maintain remission states. Surgery appears important in cases of perforation, abscesses, obstructions, or cancer management.
Actual occurrence is unknown, as there are more than Crohn's Disease and Ulcerative Colitis which appear related. It is estimated that more than 35,000 deaths were reported in 2010. Crohn's Disease alone appears to affect 3.2 per 1000 people in Europe and North America alone.
The usual onset of symptoms may appear before actual diagnoses are made, with typical diagnoses occurring between 15-30 years of age. Lead by abdominal pain symptoms (usually lower right quadrant) and the recurrent periods of flare and remission. Many dietary, bacterial, antimicrobials, and environmental factors receive attention, some new interest in evaluating alternative therapeutic modalities to deal of issues of immune system. Use of the immune privileged cellular agents held within the AD-cSVF is proposed to help with the inflammatory contributors as well as the modulation of inflammation which favors chronic wound healing and avascular systems. Known to provide secretory antibiotic (ll-37) contributions, some thought of pro- and anti-microbials, may prove of value in those areas specifically. Cytokine and growth factors implications at the lesion sites remain to be poorly understood, but those experienced in biocellular regenerative therapies have experienced contributions to healing and prevention of recurrences of ulcerative skin lesions.
Harvest of autologous of adipose-derived tissue stromal vascular fraction (AD-tSVF) is a proven rich resource of microvascular stem/stromal cell elements with well documented growth factor and cytokine contributors. With the advent of safe, measurable, and efficacious and reproducible numbers in a closed isolation environment, the ability to isolate and concentrate a cell-only product. This AD-cSVF is capable of reintroduction into patients, via a Normal Saline Solution, via parenteral route.
This study is intended to evaluate the safety (adverse outcomes) and efficacy of using autologous cellular therapy in cases of IBD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases
Keywords
IBD,Crohn's,Ulcerative Bowel; Diverticulitis;IBS;UC
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Lipoaspiration Arm 1
Arm Type
Experimental
Arm Description
Acquisition of Adipose-Derived tissue Stromal Vascular Fraction (AD-tSVF) via closed syringe harvest subdermal fat
Arm Title
AD-cSVF Arm 2
Arm Type
Experimental
Arm Description
Isolation of cellular stem/stromal cells from subdermal adipose-derived cellular stromal vascular fraction (AD-cSVF)
Arm Title
Normal Saline IV Arm 3
Arm Type
Experimental
Arm Description
Normal Saline IV with AD-cSVF cells
Intervention Type
Procedure
Intervention Name(s)
Lipoaspiration
Intervention Description
Closed Syringe Harvesting Autologous Subdermal Fat
Intervention Type
Procedure
Intervention Name(s)
AD-cSVF
Intervention Description
Use of Centricyte 1000 to isolate adipose stem/stromal cells via centrifugation
Intervention Type
Procedure
Intervention Name(s)
Normal Saline IV
Intervention Description
Normal Saline IV containing AD-cSVF
Primary Outcome Measure Information:
Title
Safety: Inflammatory Bowel Disease
Description
Inflammatory Bowel Disease to be addressed as occurrence or frequency of adverse event during study. Includes vital signs, complete blood count, and disease progression
Time Frame
12 months Evaluate Function and Adverse Events
Secondary Outcome Measure Information:
Title
Efficacy: Quality of life index , Inflammatory Bowel Disease Questionnaire(IBD-QoL)
Description
Comparison of response if it improves at least 30%
Time Frame
1 month, 6 month, 1 year
Title
Change from Baseline in C Reactive Protein (CRP)
Description
Blood draw and laboratory measure of CRP as reflection of inflammatory baseline change
Time Frame
0, 2 weeks, 8 weeks, 12 weeks
Title
Efficacy: Change in Baseline of Modified Truelove-Witts Score (MTW)
Description
Remission is considered if below 11, and response if it diminishes at least 30%
Time Frame
0, 4 weeks, 12 weeks
Title
Efficacy: Change in Baseline in Lichtiger Index
Description
Remission considered if reaching 0 point, and response if the score diminishes from pretreatment level
Time Frame
0, 12 weeks, 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients, either sex 18 years and older with confirmed diagnosis of IBD
Patients, either sex younger than 18 years upon approval of responsible parties and agreement of investigators
Ability of patient to provide informed consent (or legal guardian)
IBD diagnosed at least 6 months earlier to therapy using usual criteria
Negative pregnancy test for women of childbearing age (menarche to menopause)
Exclusion Criteria:
Mental incapacity that prevents adequate understanding of study and associate procedures and providing informed consent
Severe IBD preventing tolerance of procedures needed
Patients with impaired systemic condition, according to investigator judgment, needs immediate corticosteroid or surgical intervention
Patients that fulfill criteria of cortico-dependency and in current treatment with corticosteroids
Patients with history of colectomy
Known history of alcohol, smoking dependence or additive substance abuse
History related malignant disease - including patients participating in clinical trial with investigational drug within 6 months
Patients with known history of allergies to any substance used in this protocol
Pregnant or breastfeeding females
Presence of severe concomitant disease, in investigators opinion threatens patient's well being or safety
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert W Alexander, MD
Organizational Affiliation
Healeon Medical Inc
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Glenn C Terry, MD
Organizational Affiliation
Global Alliance for Regenerative Medicine (GARM)
Official's Role
Study Director
Facility Information:
Facility Name
Regenevita LLC
City
Stevensville
State/Province
Montana
ZIP/Postal Code
59870
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Use of Autologous, Adult Adipose-Derived Stem/Stromal Cells in Inflammatory Bowel Disease
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