Healthy volunteers test drug combo for future breast cancer treatment
NCT ID NCT07229560
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how a common antifungal drug (itraconazole) changes the way the body handles a new experimental breast cancer drug (HRS-8080). Sixteen healthy adults took HRS-8080 alone and then with itraconazole to measure drug levels and safety. The goal was to gather information for future dosing decisions, not to treat any disease.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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16 people
The number who actually took part.
- Started
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Nov 2025
- Finished
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Dec 2025
- Lead sponsor
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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 55 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 1. Aged 18-55 years; 2. Male weight ≥ 50 kg, female weight ≥ 45 kg, and body mass index (BMI): 19-28 kg/m2; 3. Normal or no clinically significant medical history, ECGs, vital signs and laboratory tests; 4. Take contraception. Exclusion Criteria: 1. Any serious clinical diseases or medical history or diseases that affect the absorption, metabolism and/or excretion of the study drug; 2. Severe infection, severe trauma or major surgery; 3. Any medications in the two weeks before screening or baseline period; 4. History of blood donation or severe blood loss; 5. Have been vaccinated within 3 months before the screening or baseline period; 6. History of smoking or excessive alcohol or drug abuse; 7. History of excessive amounts of tea, coffee or caffeinated beverages, special foods; or have special dietary requirements; 8. Other situations in which the researcher judges unsuitable.
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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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The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, 450052, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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