New Low-Cost radiation therapy could make liver cancer treatment accessible for all
NCT ID NCT07436988
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a new, affordable type of radioactive microsphere for treating liver cancer that cannot be removed by surgery. The microspheres are delivered directly to the tumor through a blood vessel, delivering radiation to kill cancer cells. The trial will enroll 18 adults with advanced liver cancer to check for safety and side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- radioactive microspheres (labeled with rhenium-188 or lutetium-177)
- What this could lead to
- If successful, this could provide a safe, effective, and low-cost treatment option for liver cancer patients who cannot have surgery.
- What could go wrong
- This is a very early Phase 1 safety trial with only 18 participants, so it is too soon to know if the treatment works or is safe long-term.
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
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 18 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
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 to 90 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.
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. Age greater than or equal to 18 years (male or female) 2. Histologically or radiologically confirmed diagnosis of HCC deemed inoperable 3. Barcelona Clinic Liver Cancer stage B with ECOG performance status between 0 and 2 4. At least one measurable lesion with longest diameter greater than or equal to 5 cm on cross sectional imaging 5. Portal vein thrombosis may be present or absent 6. Laboratory criteria: 1. Serum creatinine less than or equal to 1.5 mg per dL 2. Total bilirubin less than or equal to 2.0 mg per dL 3. AST or ALT less than or equal to 5 times upper limit of normal 4. Leukocyte count greater than or equal to 1500 per microliter 5. Platelet count greater than or equal to 50000 per microliter 6. Prothrombin time less than or equal to 1.3 times control or INR less than or equal to 1.5 7. Karnofsky performance status greater than 70 8. Ability and willingness to provide written informed consent for participation in the IEC approved protocol Exclusion Criteria: 1. Women of childbearing potential who are unwilling or unable to use effective contraception or who are pregnant or lactating 2. Child Pugh class C liver function 3. Presence of extrahepatic metastases 4. Severe chronic pulmonary disease with hypoxemia or NYHA class three or four heart failure 5. Myocardial infarction within the past six months 6. Unstable arrhythmia or symptomatic cardiac disease 7. Any other serious uncontrolled illness that in the investigator's opinion would compromise study participation 8. History of other malignancy except adequately treated basal cell carcinoma or cervical carcinoma in situ within the last five years 9. Major surgery within four weeks prior to enrolment 10. Active uncontrolled bacterial infection requiring systemic therapy 11. Liver rupture, tumor penetration of the liver capsule, tumor invasion of the biliary system, or biliary obstruction 12. Known allergy or hypersensitivity to any component of the investigational or comparator microspheres 13. Prior treatment with Selective Internal Radiation Therapy (SIRT) 14. Estimated overall survival less than one month
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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
5 sites. 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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All India Institute of Medical Sciences
Bhubaneswar, Odisha, 751019, India
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All India Institute of Medical Sciences
Delhi, South Delhi, 110029, India
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Jawaharlal Institute of Postgraduate Medical Education and Research
Puducherry, Puducherry, 605006, India
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Postgraduate Institute of Medical Education and Research
Chandigarh, Chandigarh, 160012, India
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Tata Memorial Hospital
Mumbai, Maharashtra, 400012, India
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Experimental pill SHY-ONC6 takes on Hard-to-Treat cancers
- New drug cocktail aims to shrink liver cancer lung tumors
- New cocktail therapy targets tough liver cancer with blood clot
- New blood test could spot liver cancer sooner
- Liver cancer showdown: which combo causes less harm?
- AI tool aims to predict liver cancer return after surgery