Using medical cannabis to relieve symptoms in patients with advanced pancreatic cancer
Official title: A Randomized Phase II Trial of Medical Cannabis to Reduce Symptom Burden in Patients With Advanced Pancreatic and Colorectal Cancer (CanPan-C)
Run by HealthPartners Institute · NCT06605430 · Data updated 2026-11-12
This study is testing if medical cannabis can help relieve symptoms like pain and nausea in people with advanced pancreatic cancer.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 64 (estimated) |
| Sponsor | HealthPartners Institute Academic / other |
| Drugs / interventions | chemotherapy, immunotherapy |
| Locations | 1 site (Saint Louis Park, Minnesota) |
| Status | Recruiting |
| Started | September 16, 2024 |
| Main results expected | December 2027 |
| Study ends | January 2028 |
| Registry record updated | October 14, 2026 |
| Trial ID | NCT06605430 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 or older with advanced PDAC who are experiencing significant symptoms and are starting systemic chemotherapy.
✕Probably not a fit
Patients who do not experience significant symptoms or who are not residents of Minnesota may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the effects of medical cannabis on symptom burden in patients with advanced pancreatic ductal adenocarcinoma (PDAC). Participants will be randomly assigned to receive medical cannabis either immediately or after an 8-week delay, allowing researchers to compare symptom relief and quality of life outcomes between the two groups. The study will assess patient-reported outcomes and safety signals over a 16-week period, with a focus on understanding how cannabis can alleviate symptoms like nausea, pain, and anorexia. The goal is to provide evidence for a potential new treatment option for managing difficult symptoms associated with PDAC.
Why it matters
Potential benefit: If successful, this study could provide a new therapeutic option for managing symptoms in patients with advanced pancreatic cancer, potentially improving their quality of life.
How similar studies have gone: While the use of medical cannabis for symptom management in cancer patients is being explored, this specific approach in advanced PDAC is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria 1. Adults (aged 18 or more at enrollment) 2. Histologically or cytologically proven pancreatic or colorectal cancer. Histologies may include listing of adenocarcinoma, poorly differentiated carcinoma, or other pathology terms that treating oncologist would consider managing per usual standard of care of pancreas and colorectal adenocarcinoma. Neuroendocrine tumors are excluded in both cancer types. 3. Advanced stage (locally advanced or metastatic) pancreatic or colorectal cancer with no definitive plans for curative surgery in the next 3 months 4. Self-report of experiencing nausea, vomiting, anorexia, cachexia (wasting), or pain at least once in the 14 days prior to randomization 5. Plan to initiate or initiated within the past 2 weeks standard-of-care systemic chemotherapy (any regimen that does not include immunotherapy) at a participating institution with no prior systemic therapy in the prior 3 months (prior adjuvant or neoadjuvant chemotherapy is allowed as long as it was \>3 months prior to randomization) 6. Must be a resident of Minnesota 7. Must be willing to be registered in the Minnesota Medical Cannabis Program and follow all rules and requirements of the state program 8. Must be willing to report baseline and required patient-reported outcomes Exclusion Criteria 1. Self-reported regular use (using 10 or more days in the 30 days prior to randomization) of a THC containing cannabinoid product 2. Patients with a history of intolerance or hypersensitivity to cannabis (i.e., cannabis hyperemesis) 3. Patients with Alzheimer's dementia, active epilepsy, or history of traumatic brain injury 4. Patients with known active or untreated brain metastases. A brain MRI is not required during the screening period. 5. Patients initiating or receiving immunotherapy, a chemotherapy-immunotherapy combination, or non-standard cytotoxic chemotherapy (including patients enrolled/ enrolling in trials of investigational cancer-directed treatments) 6. Women who are pregnant, breastfeeding or of childbearing potential without the use of birth control 7. Uncontrolled acute or chronic medical conditions, psychiatric conditions or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for enrollment in this study 8. Has any condition that in the opinion of the investigator might jeopardize the safety of the subject or interfere with protocol compliance
Where it's running
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HealthPartners Cancer Research Center
Saint Louis Park, Minnesota, United States Recruiting
Study contacts
- Study coordinator: Alissa Gavenda, RN
- Email: cancercannabis@HealthPartners.com
- Phone: (952) 977-5555
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.