New PET tracer could reveal hidden cancer clues without a biopsy
NCT ID NCT07459192
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a new radioactive tracer called 68Ga-DOTA-BLP for PET scans to see PD-L1 levels in tumors. PD-L1 helps cancer hide from the immune system, and knowing its levels can guide immunotherapy. The study will include 50 adults with confirmed cancer and suspicious spots on scans. The goal is to see if this imaging method is accurate and safe.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 68Ga-DOTA-BLP (a radioactive tracer for PET scans)
- What this could lead to
- If successful, this could lead to a more accurate, non-invasive way to see PD-L1 levels in tumors, helping doctors choose the right immunotherapy for each patient.
- What could go wrong
- This is a small, early-stage study (50 people) that hasn't started yet. The new imaging method may not be more accurate than existing tests, and results may not apply to all cancer types.
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.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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.
Who is studied
Patients with malignant tumors confirmed by biopsy or surgical pathology.
- 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: * Age over 18 years, gender not restricted; * patients with malignant tumors confirmed by biopsy or surgical pathology; * Imaging findings of suspicious lymph nodes or distant metastases; * informed consent signed in writing by the subject or his/her legal guardian. Exclusion Criteria: * patients who have received antitumor therapy prior to PET/CT or PET/MR scanning; * Patients with severe medical conditions who cannot tolerate PET/CT or PET/MR scans; * The alternative subjects have contraindications to PET/CT or PET/MR scans; * exposure to radiation of more than 50 mSv in the past year; * The alternative subjects underwent major surgery within the past 3 months; received experimental drug or device therapy (with unclear efficacy or safety) within the past 1 month; * The alternative subjects had any clinical conditions that the principal investigator of this study considered to be potentially harmful or associated with the formulation.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Daping Hospital, Army Medical University
Chongqing, Chognqing, 400010, China
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