Promising pancreatic cancer drug study halted before it began
NCT ID NCT07026916
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study was designed to test a new drug called GFH375 in people with advanced pancreatic cancer that has a specific genetic change (KRAS G12D). The goal was to see if the drug could shrink tumors or slow the disease. However, the study was withdrawn before any participants were enrolled, so no results are available.
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.
- Expected to start
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Aug 2025
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 75 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Subjects must voluntarily agree to participate in the trial and sign a written informed consent form. 2. Male or female ≥ 18 years old and ≤75 years old. 3. With histologically or cytologically confirmed metastatic pancreatic cancer harboring KRAS G12D mutation 4. Be able to provide tumor tissue samples that meet the requirements 5. Have at least one measurable lesion according to RECIST1.1 6. ECOG performance status of 0-1. 7. With a life expectancy of ≥12 weeks. 8. Adequate laboratory parameters during the screening period. Exclusion Criteria: 1. Active brain metastases. 2. Prior treatment with a KRAS G12D inhibitor or a pan-RAS/KRAS inhibitor. 3. With poorly controlled or severe cardiovascular disease. 4. Subjects with active hepatitis B or active hepatitis C. 5. Known allergy to the study drug or its components. 6. Pregnant or lactating women.
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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.
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Other studies related to the condition(s) this trial covers.
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