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Chronic PancreatitisEarly Phase 1STEMCAP-1NCT06205342

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

A Early Phase 1 study testing Mesenchymal Stem Cells in people with Chronic Pancreatitis and Chronic Pain, run by Medical University of South Carolina at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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 more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Chronic Pancreatitis, Chronic Pain
What is being tested?
Mesenchymal Stem Cells
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
48 participants
Where
1 siteUnited States
Study dates
17 Jul 2024to 1 Jun 2028
Phase
Early Phase 1
Are there results?
Not yet: the study is under way

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 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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:
  • abdominal pain suggestive of pancreatitis,
  • serum amylase or lipase level greater than three times the upper normal value, or
  • characteristic imaging findings.
  • Chronic pain syndromes other than pancreatitis that require daily use of opioids in the past 30 days.
Show all 23Show fewer
  • Severe organ failure(s) likely to interfere with clinical pain outcomes within 6 months.
  • HbA1c >12%
  • 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.
  • New York Heart Association grade 3 congestive heart failure.
  • Current lung, hematologic, or solid organ malignancy other than skin or cervical Stage 1 cancers within the past 3 years.
  • Subjects with current infection with Hepatitis B, C or HIV infection.
  • Active malignancy with the exception of non-melanoma skin cancer.
  • Subjects who have had any ongoing alcohol abuse and/or any illegal drug abuse within the past 6 months.
  • 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.
  • 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.
  • 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.
  • Subjects with infected pancreatic pseudocysts or pancreatic walled-off necrotic areas at the time of consent
  • 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
  • Breastfeeding females
  • Subject unwilling to follow the protocol and assessments

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Leah Benn, MPH contact

843-792-2813

bennle@musc.edu

United States1 site, 1 recruiting
  • Medical University of South Carolina

    Charleston, South Carolina, 29425

    Hongjun Wang, Ph.D., 843-792-1800, wangho@musc.edu

    Charlton Strange III, MD, (843) 792-3174, strangec@musc.edu

    Recruiting

Other trials in United States

About this study

Official title: STEMCAP-1: Safety and Efficacy of Mesenchymal Stem Cells Associated With Chronic Pancreatitis Pain

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.

Being tested
Mesenchymal Stem Cells, Other: Placebo
Medical subject headings
Pancreatitis, Chronic, Chronic Pain

What participants receive

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

  • Mesenchymal Stem CellsDrug

    Also called MSCs

    Autologous bone marrow derived MSCs

  • Other: PlaceboOther

    Also called Controls

    Control

Study groups in NCT06205342
Study groupRoleWhat they receive
Experimental CohortExperimentalMSC
Receives: Drug: Mesenchymal Stem Cells
Validation CohortPlacebo comparatorPlacebo
Receives: Other: Other: Placebo

What is being measured

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

  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).

    Measured: 6 months

Secondary outcomes (4)
  1. Change in pancreatic volume measured by blinded scoring of MRI

    Pancreas volume change

    Measured: Screening, 6 month

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

    Average Daily morphine Equivalent

    Measured: 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)

    Measured: 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)

    Measured: Screening, 1 month, 3 month, 6 month

Timeline

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

  1. First posted16 Jan 2024
  2. Study start17 Jul 2024
  3. Primary completion1 Jun 2027 (estimated)
  4. Study completion1 Jun 2028 (estimated)

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
Early Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a pilot, randomized, double-blind, placebo-controlled, stratified randomization study to determine the efficacy of a single intravenous infusion of allogeneic bone marrow-derived mesenchymal stromal cells in subjects with painful chronic pancreatitis (CP).
Masking
Triple blind
Who is masked
Participant, Care provider, Outcomes assessor
Enrolment
48 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06205342
Sponsor's protocol ID
PRO 00132905
Other IDs
1UG3DK136705-01
Acronym
STEMCAP-1
Status last verified
Apr 2026
First submitted
4 Jan 2024
Last updated
30 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Mesenchymal Stem Cells in people with Chronic Pancreatitis and Chronic Pain, run by Medical University of South Carolina at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 23 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Leah Benn, MPH (843-792-2813, bennle@musc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Izbicki pain score (M6 vs. Baseline) (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2026.

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