Can a common diabetes drug help pancreatic cancer patients control blood sugar?
NCT ID NCT06168812
First seen Jun 27, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This phase 2 trial is testing the safety and effectiveness of glipizide, a standard diabetes drug, for lowering blood sugar in people with pancreatic cancer. The study includes 29 participants with active pancreatic cancer and high blood sugar. Researchers will measure blood sugar levels before and after starting glipizide to see if it helps control hyperglycemia.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- glipizide (a sulfonylurea drug that helps lower blood sugar)
- What this could lead to
- If successful, this could provide a safe and effective way to manage high blood sugar in people with pancreatic cancer, improving their overall care.
- What could go wrong
- This is a small, early-phase trial with only 29 participants, so results may not apply to everyone. Glipizide can cause low blood sugar, and its long-term effects in this specific group are not yet known.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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29 people
The number who actually took part.
- Started
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Dec 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Cohort 1 * Age ≥18 years * Biopsy-proven PDAC * Radiological evidence and clinical assessment that patient has active disease (local, locally advanced, or metastatic) * Willing and able to comply with the requirements of the protocol * Willing to use their bluetooth-enabled wifi or cellular mobile device * Hemoglobin A1c (HbA1c) \> 7%, or fructosamine \> 287 mg/dL, or random glucose \> 180 mg/dL, or strong clinical suspicion that patient has hyperglycemia, making it reasonable to expect their mean daily glucose is ≥154 mg/dL * Eastern Cooperative Oncology Group performance status ≤2 * BMI \<30 kg/m2 Cohort 2a * Age ≥18 years * Biopsy-proven PDAC * Radiological evidence and clinical assessment that patient has active disease (local, locally advanced, or metastatic pancreatic cancer) * Clinical diagnosis of diabetes mellitus * Active care at MSK (defined as at least 1 physician or APP encounter every 3 months) for PDAC during the period from which data were recorded in the electronic medical record (in this retrospective study patients need not be under active care at the time the research is conducted) * At least 1 electronic prescription for a sulfonylurea (glipizide, glimepiride, or glyburide) or metformin * Three-month baseline period before metformin or sulfonylurea initiation in which the participant does not receive either drug class or insulin * Body weight recorded within 3 months before start of metformin or a sulfonylurea Cohort 2b * Age ≥18 years * Biopsy-proven PDAC * Radiological evidence and clinical assessment that patient has active disease (local, locally advanced, or metastatic) * Active care at MSK (defined as at least 1 physician or APP encounter every 3 months) for PDAC during the period of data collection * Apparent current use based on chart review of metformin (but not sulfonylurea); sulfonylurea (but not metformin); or neither drug Exclusion Criteria: Cohort 1 * Use during the past month of any antidiabetic medication other than metformin at home (sporadic use \[fewer than 1 of 7 days during the past month\] is permitted) * Changes in metformin dose in the past month * History of sulfonylurea intolerance or allergy * History of severe hypoglycemia (hypoglycemia requiring emergency medical assistance, emergency room or urgent care visit, or hospital admission) * AST or ALT \>3 x upper limit of normal * Glomerular filtration rate \<30 mL/min/1.73m2 * Daily chronic use of any dose of corticosteroids (as distinct from intermittent exposure to steroids as part of cyclic chemotherapy) * Inability to wear CGM Cohort 2a * Greater than trace ascites documented on imaging or physical exam Cohort 2b * Greater than trace ascites documented on imaging or physical exam
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey, 07645, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited protocol activities)
Commack, New York, 11725, United States
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Memorial Sloan Kettering Monmouth (Limited protocol activities)
Middletown, New Jersey, 07748, United States
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Memorial Sloan Kettering Nassau (Limited Protocol Activities)
Uniondale, New York, 11553, United States
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Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York, 10604, United States
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Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey, 07920, United States
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