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RecruitingNCT06205342STEMCAP-1Updated Sep 30, 2026

Safety and Efficacy of Mesenchymal Stem Cells Associated With Chronic Pancreatitis Pain

An Early Phase 1 interventional study of Mesenchymal Stem Cells and Other: Placebo in Chronic Pancreatitis and Chronic Pain, sponsored by Medical University of South Carolina. Recruiting at 1 site in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Medical University of South Carolina · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This protocol aims to test whether an infusion of allogeneic bone marrow-derived mesenchymal stromal cells (BM-MSCs) can reduce pain associated with chronic pancreatitis (CP) and explore potential mechanisms of MSC action.

Read the detailed description

Chronic pancreatitis (CP) and chronic pain: CP is a debilitating disease characterized by persistent pancreatic inflammation, irreversible morphological changes (fibrosis) in the pancreas and severe chronic pain. A progressive loss of exocrine and endocrine function occurs during disease progression. The incidence of CP ranges from 1.6 to 23 cases per 100,000 populations per year worldwide and is likely under diagnosed in the general population. CP in the United States results in more than 122,000 outpatient visits and more than 56,000 hospitalizations per year. The poorly understood pathophysiology of CP makes the identification of means to treat the underlying cellular disorder problematic. Abdominal pain has been reported in at least 80-94% of patients. The pain suffered by CP patients is among the worst encountered in medicine, which often leads to opioid addiction. Many CP patients require hospital admission at some stage in their illness. The cause of pain is complex and is mostly unknown. The pathophysiology in pain due to CP is multifactorial, including peripheral nociception, peripheral/pancreatic neuropathy, and neuroplasticity. Achieving satisfactory pain relief remains a challenge. Current management strategies have used a step-up approach in pain medications that often lead to opioid dependence. Among all patients, 40-75% patients will eventually require surgery, after which only 34-52% attain pain relief after pancreas resection. CP pain provides a useful model for the understanding of the mechanisms and treatment of pain syndromes with an identifiable nociceptive source in general as approximately 50 million U.S. adults are suffering from pain. Improving the management of CP pain may translate to other disease states with pain and opioid addiction.

Mesenchymal stromal cells (MSCs) are adult stem cells that can be harvested and expanded for therapy. MSC therapy is an investigational intervention for CP. There is increasing evidence that MSC therapy can effectively target several injury pathways in a variety of fibroinflammatory diseases and can reduce pain while suppressing inflammation, something that most pharmacological interventions cannot accomplish. Data from animal models and clinical trials support the outstanding and durable effects of MSC infusion in the suppression of chronic neurological pain and inflammation associated with knee osteoarthritis, critical limb ischemia, neuropathy, diabetic neuropathy, and others. MSCs migrate to the spinal cord and pre-frontal cortex of neuropathic mice after injection and exert pain relief. A recent study demonstrated that infusion of human MSCs significantly reduced pain, improved pancreatic volume, and reduced fibrosis in CP rodent models.

Rationale of the study: Because MSCs are a novel therapy that may improve chronic pancreatitis pain in animal models and improve chronic pain in other human disease states, these cells are worthy of study. This pilot study will give participants MSCs or placebo for CP subjects with pain. This study will inform future study designs and may lead to MSCs as a standard of care if they are safe and effective.

02

Conditions studied

  • Chronic Pancreatitis
  • Chronic Pain
03

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age between 18 and 75 years old, male or female
  2. Definite chronic pancreatitis, using M-ANNHEIM criteria
  3. Patients who are diagnosed with painful CP for more than 6 months may be constant or may have been waxing and waning/remitting.
  4. Baseline Izbicki pain score > 30
  5. Stable dose of opioids for the past 30 days

Exclusion criteria

Exclusion criteria:

  1. Acute pancreatitis per 2012 revised Atlanta criteria within the last 30 days.

    The revised Atlanta classification requires that two or more of the following criteria be met for the diagnosis of acute pancreatitis:

    1. abdominal pain suggestive of pancreatitis,
    2. serum amylase or lipase level greater than three times the upper normal value, or
    3. characteristic imaging findings.
  2. Chronic pain syndromes other than pancreatitis that require daily use of opioids in the past 30 days.
  3. Severe organ failure(s) likely to interfere with clinical pain outcomes within 6 months.
  4. HbA1c >12%
  5. Laboratory values of WBC \< 2.0 cells/10\^3, HgB \< 8gm/dl and platelets \< 50K, AST or ALT >3 times the upper limit of normal, and Creatine> 2.0mg/dl. Laboratory valuate may be retested at a later date and if they are no longer exclusionary, the subject may be enrolled.
  6. New York Heart Association grade 3 congestive heart failure.
  7. Current lung, hematologic, or solid organ malignancy other than skin or cervical Stage 1 cancers within the past 3 years.
  8. Subjects with current infection with Hepatitis B, C or HIV infection.
  9. Active malignancy with the exception of non-melanoma skin cancer.
  10. Subjects who have had any ongoing alcohol abuse and/or any illegal drug abuse within the past 6 months.
  11. Any subject who has received an investigational drug or device within 30 days before randomization or who is expected to receive an investigational drug or device during this study.
  12. Patients with planned endoscopic or surgical intervention, surgical resection or needle drainage of pancreatic structures in the next 6 months.

    • Cases where participants initially meet inclusion criteria, but subsequently are felt to need a surgical or endoscopic intervention during the study will be reviewed by the medical monitor - as providing optimal care to the patient is the priority. Individuals who do receive these interventions during their 6-month participation in the study will be censored from outcome evaluation.
  13. Patients who have had a pancreatic surgery, endoscopic procedure with therapy, or hospitalization related to pancreatitis within the last 90 days.

    • In the case that a patient is screen-failed due to this criterion, they may be re-screened after the 90-day period has ended if all other eligibility criteria are met.
  14. Subjects with infected pancreatic pseudocysts or pancreatic walled-off necrotic areas at the time of consent
  15. Females who are pregnant or women of childbearing potential (WOCBP) and males with female partners of childbearing potential who are not willing to use adequate contraception during the study
  16. Breastfeeding females
  17. Subject unwilling to follow the protocol and assessments
04

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    Experimental Cohort

    MSC

    Drug: Mesenchymal Stem Cells

  • Placebo comparator
    Validation Cohort

    Placebo

    Other: Other: Placebo

Interventions

  • DrugMesenchymal Stem Cells

    Autologous bone marrow derived MSCs

    Also known as: MSCs

  • OtherOther: Placebo

    Control

    Also known as: Controls

05

What researchers measure

Primary outcomes

  1. Change in Izbicki pain score (M6 vs. Baseline)

    Change in pain as measured by Izbicki pain scores, a validated score for pain in chronic pancreatitis, consist of 4 questions, with a range of 0 (no pain) to 100 (severe, debilitating pain).

    Time frame: 6 months

Secondary outcomes

  1. Change in pancreatic volume measured by blinded scoring of MRI

    Pancreas volume change

    Time frame: Screening, 6 month

  2. Change in opioid use as measured in average daily morphine equivalents.

    Average Daily morphine Equivalent

    Time frame: Screening, 1 month, 3 month, 6 month

  3. Changes in quality of life

    Quality of life to be measured by Promise-29-v 2.1 (with generated T-score for each domain)

    Time frame: Screening, 1 month, 3 month, 6 month

  4. Change in M-Manheim Severity Index absolute score

    Severity of Index absolute scores (with lowest severity 0 and highest severity 24 points)

    Time frame: Screening, 1 month, 3 month, 6 month

06

Study locations

1 of 1 sites recruiting
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
    • Hongjun Wang, Ph.D. · Contact · wangho@musc.edu · 843-792-1800
    • Charlton Strange III, MD · Contact · strangec@musc.edu · (843) 792-3174
    • Hongjun Wang, Ph.D. · Principal investigator
    • Charlton Strange III, MD · Sub investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06205342
Lead sponsor
Medical University of South Carolina
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Responsible party
Hongjun Wang (Professor-Faculty, Medical University of South Carolina) — Principal investigator
First posted
Jan 16, 2024
Start date
Jul 17, 2024
Primary completion
Jun 1, 2027 (estimated)
Completion
Jun 1, 2028 (estimated)
Last update
Sep 30, 2026

Study contacts

Leah Benn, MPH
Contact
bennle@musc.edu
843-792-2813
Sarah Miller
Contact
dicksosa@musc.edu
(843) 792-6388
Hongjun Wang, PhD
principal investigator · Medical University of South Carolina

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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