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Mission: Cure

Cycle 2

Chronic pancreatitis is the inflammation of the pancreas, the organ that produces digestive enzymes and insulin. The continued inflammation leads to permanent damage and scarring of the pancreas. This scarring causes digestive problems and eventually leads to diabetes. Chronic pancreatitis patients experience extreme abdominal pain and are at exceptionally high risk for pancreatic cancer.

Last updated 04/30/2026

Clinical

Disease Class
Abdominal surgical diseases
Channelopathies
Diseases due to toxic effects
Endocrine diseases
Gastroenterological diseases
Genetic diseases
Body Systems
Digestive
Endocrine
Organs
Pancreas
Known Genetic Link
Yes, there are both genes that cause the condition and genetic factors that contribute
Causative Genes
PRSS1
Contributory Genes
CASR
CEL
CFTR
CLDN2
CTRC
SPINK1
Type of Inheritance
Autosomal dominant
Not specified / unknown
Newborn Screening
No
Disease Mechanism(s)
Aberrant immune response
Abnormal channel regulation
Abnormal protein degradation
Autoimmune Disease
Autophagy defect
Extracellular matrix abnormality
Ion channel dysfunction
Other
Protein misfolding
Age of Onset
Adolescence (12-17)
Adulthood (age 18-64)
Early childhood (age 1+-5)
Elderly (age 65+)
Infancy (age 0-1)
Middle childhood (6-11)
Average Age at Diagnosis
Adulthood (age 18-64)
Life Expectancy
Adulthood (age 18-64)
Affected Sex(es)
Female
Intersex
Male
National Prevalence
10000+
Global Prevalence
10000+
National Incidence
11-50
Global Incidence
11-50
Populations and/or ancestry with higher prevalence
Higher average incidence for Black people
Symptoms / Phenotypes
diabetes
diarrhea
fatigue
malnutrition
pain, abdominal
pain, chronic
vomiting / nausea
weight loss
Biomarkers
None
Existing Therapies
Complementary and Alternative treatments
· Diet Modification, Nutritional Supplements (curcumin, Vitamin D, N-Acetyl Cystene), Meditation, Cognitive Behavioral Therapy
Off-Label Drug Use
Regulatory Agency-Approved for Symptom Relief
· Analgesics including opioid pain medicines; Pancreatic enzyme replacement therapy (PERT; pancrelipase) for exocrine pancreatic insufficiency (malabsorption/steatorrhea), e.g., Zenpep / Creon
Regulatory Agency-Approved to Cure or Modify the Disease
· Tryngolza (olezarsen) (only for pancreatitis caused by FCS); Redemplo (plozasiran) (only for pancreatitis caused by FCS)
Therapies in Development
Antibody-based therapy (monoclonal antibodies, biologics)
· 2, TRIV-920, Not disclosed
Cellular therapies (stem cell transplants, CAR-T therapies, etc.)
· 1, Mesenchymal Stem Cells
Dietary & metabolic therapies (medical food, dietary restriction, supplements, etc.)
Gene therapy
· 1, PRSS1 Gene Therapy
Repurposed drug
· 5+, Ivacaftor, Simvastatin, Paricalcitol, Pirfenidone, Tocilizumab
Small molecule therapy (novel small molecule drugs)
· 2, Proglumide, Not disclosed
Surgical & interventional
Therapeutic Development Stages
Approved/Available
In clinical trials (Phase I, II, III, or IV)
In preclinical development
In research/exploratory phase
Therapeutic Development Role
None

Organizational & Research

Cell Lines
None
Cell Lines, Institution
None
Cell Lines, share
N/A
Disease Model
Organoids
Disease Model, Involvement
Consulted
Disease Model, share
No
Organizational Challenges
Venture philanthropy and other innovative financing models
Clinical Trial Role
Funding
Meeting with regulators
Outcome measures, development
Recruitment and outreach, patients
Recruitment and outreach, trial sites/physicians
Results dissemination, publication
Study material design, review (not protocol)
Study protocol design, review
Clinical Trial Types
Observational
Phase 1
Phase 2
Biobank, Institution
None
Center of Excellence, Institution
Johns Hopkins Hospital
Center of Excellence, Involvement
Consulted
Funded
Registry
No, we do not have a registry and have no plans to create one
Natural History Study
No, we do not have a natural history study, but we plan to create or collaborate on one
FDA Patient Listening Session
Yes
FDA Patient-Focused Drug Development (PFDD) Program
Yes
ICD Codes
We use an ICD-10 code capturing the family of diseases to which our disease belongs
We use an ICD-11 code capturing the family of diseases to which our disease belongs
Diagnostic Guidelines
Yes, we have guidance available on our website
Science Advisory Board Policies
Does not have an SAB
Research Network Policies
Does not have a CRN
Patient Priority Survey
Yes
Patient Priority Survey, share
Yes, will share
Research Roadmap
Yes we have a Research Roadmap, and will share policies
International Chapters
None
International Partners
Europe
Middle East
Other International Research Initiatives
None