New PET scan probe could sharpen lung cancer detection
NCT ID NCT07508852
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing a new radioactive probe called PFD3, used with a PET/CT scan, to see if it can better find and assess small cell lung cancer (SCLC) by targeting a protein called DLL3 found on cancer cells. About 30 adults with SCLC will receive both a standard FDG scan and the new PFD3 scan to compare their accuracy. The goal is to improve diagnosis and monitoring of this aggressive cancer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 68Ga-PFD3 (a radioactive probe for PET/CT imaging)
- What this could lead to
- If successful, this could provide a more accurate way to diagnose and monitor small cell lung cancer, potentially guiding better treatment decisions.
- What could go wrong
- This is an early-phase trial with only 30 participants, so results may not apply to everyone. The probe's safety and effectiveness are still being tested.
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 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- 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.
- 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: * Adults. * Histologically confirmed small cell lung cancer (SCLC). * At least one measurable lesion ≥1 cm in diameter (primary tumor, metastatic lesion, or involved lymph node) confirmed by standard imaging modalities. * Laboratory tests (complete blood count and biochemical analysis) completed within 4 weeks prior to enrollment. Exclusion Criteria: * Pregnancy. * Breastfeeding. * Acute psychiatric disorders. * Inability to undergo PET scanning (e.g., due to claustrophobia, weight limits, or other medical contraindications). * Inability to complete the study procedures as anticipated. * Prior therapy targeting DLL3.
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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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Peking university first hospital nuclear medicine
RECRUITINGBeijing, Beijing Municipality, 100034, China
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