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.
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.
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- 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.
United States1 site, 1 recruiting
- 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
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.
- Conditions
- Chronic Pancreatitis, Chronic Pain
- 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 group | Role | What they receive |
|---|---|---|
| Experimental Cohort | Experimental | MSC Receives: Drug: Mesenchymal Stem Cells |
| Validation Cohort | Placebo comparator | Placebo Receives: Other: Other: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
Change in pancreatic volume measured by blinded scoring of MRI
Pancreas volume change
Measured: Screening, 6 month
Change in opioid use as measured in average daily morphine equivalents.
Average Daily morphine Equivalent
Measured: Screening, 1 month, 3 month, 6 month
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
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.
- First posted16 Jan 2024
- Study start17 Jul 2024
- Primary completion1 Jun 2027 (estimated)
- Study completion1 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic PancreatitisStudies of the same condition, open and under way.
- More trials run by Medical University of South CarolinaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Medical University of South Carolina
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Hongjun Wang, Medical University of South Carolina
- Investigators
- Hongjun Wang, PhD, Principal investigator, Medical University of South Carolina
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
Study at a glance
From the registry record, last updated by the sponsor on 30 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- STEMCAP-1: Safety and Efficacy of Mesenchymal Stem Cells Associated With Chronic Pancreatitis Pain
- ClinicalTrials.gov ID
- NCT06205342
- Acronym / sponsor ID
- STEMCAP-1 / PRO 00132905
- Conditions
- Chronic Pancreatitis, Chronic Pain
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 48 participants (estimated)
- Lead sponsor
- Medical University of South CarolinaUniversity, hospital or other
- Collaborators
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Study start
- 17 Jul 2024 (actual)
- Primary completion
- 1 Jun 2027 (estimated)
- Study completion
- 1 Jun 2028 (estimated)
- First posted
- 16 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, outcomes assessor)
- Number of arms
- 2
- 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).
| Arm | Type | Receives |
|---|---|---|
| Experimental Cohort | Experimental | Drug: Mesenchymal Stem CellsMSC |
| Validation Cohort | Placebo comparator | Other: Other: PlaceboPlacebo |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (23 listed)
- 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:
- Chronic pain syndromes other than pancreatitis that require daily use of opioids in the past 30 days.
- Severe organ failure(s) likely to interfere with clinical pain outcomes within 6 months.
- HbA1c >12%
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mesenchymal Stem CellsAlso: MSCsAutologous bone marrow derived MSCs | Drug | Experimental Cohort |
| Other: PlaceboAlso: ControlsControl | Other | Validation Cohort |
Primary outcome
Change in Izbicki pain score (M6 vs. Baseline)
Time frame: 6 months
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).
4 secondary outcomes
Change in pancreatic volume measured by blinded scoring of MRI
Time frame: Screening, 6 month
Change in opioid use as measured in average daily morphine equivalents.
Time frame: Screening, 1 month, 3 month, 6 month
Changes in quality of life
Time frame: Screening, 1 month, 3 month, 6 month
Change in M-Manheim Severity Index absolute score
Time frame: Screening, 1 month, 3 month, 6 month
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Hongjun Wang, PhD principal investigator
Medical University of South Carolina
1 site in 1 country: see every site and its status.
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.