New combo tackles tough pancreatic cancer
NCT ID NCT05052723
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This phase 2 trial tested two drugs, cabozantinib and pembrolizumab, in 21 people with metastatic pancreatic cancer that had worsened after standard treatment. The goal was to see if the combination could slow cancer growth. The study is complete, and results may help guide future research.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cabozantinib and pembrolizumab
- What this could lead to
- If successful, this combination could offer a new treatment option for people with advanced pancreatic cancer that has not responded to standard therapies.
- What could go wrong
- This is a small, early-phase trial with only 21 participants, so results may not apply to everyone. The drugs can cause side effects, and the cancer may still progress.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
21 people
The number who actually took part.
- Started
-
Jan 2022
- Finished
-
Nov 2024
- Lead sponsor
-
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
-
18 to 99 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * Diagnosis of pancreatic ductal adenocarcinoma * Evidence of progression or intolerance to previous standard of care pancreatic cancer systemic or locoregional therapies * Patients must have adequate organ function Exclusion Criteria: * Chemotherapy or other locoregional anti-tumoral therapies performed within 28 days of study treatment initiation * Received palliative radiation therapy within 2 weeks or any other radiation therapy within 4 weeks of start of study intervention * Has received prior systemic anti-cancer therapy including investigational agents within 4 weeks prior to allocation * Has a diagnosis of immunodeficiency (autoimmune disease) or is receiving chronic systemic steroid therapy * Clinically significant cardiovascular disease * Uncontrolled hypertension * Inability to swallow tablets
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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
-
University of Kentucky Markey Cancer Center
Lexington, Kentucky, 40536, United States
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