Could a heart pill help lung cancer patients live longer?
NCT ID NCT07261098
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a drug called sacubitril/valsartan, already used for heart failure and high blood pressure, can help people with advanced lung cancer who also have high blood pressure. The goal is to see if it reduces the risk of death and heart problems. About 200 adults with stage III or IV lung cancer and a history of hypertension will take the drug and be followed over time.
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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.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 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 80 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: * Able to provide written informed consent (ICF) and able to understand and comply with the study requirements and assessment schedule. * Male or female aged ≥18 years and \< 80years at the time of signing the ICF. * Histologically or cytologically confirmed advanced lung cancer (TNM III-TNM IV) based on the 8th edition of the AJCC staging system * Patients were diagnosed hypertension before the diagnosis of advanced lung cancer * ECOG performance status score ≤ 1. * Adequate organ function during the screening period Exclusion Criteria: * Predicted survival period less than 12 months * Female patients if pregnant. * Hypersensitivity to any component of ARNI * Severe renal dysfunction (eGFR\<30ml/min/1.73m2) * Severe liver dysfunction (Child-Pugh C) * Bilateral renal artery stenosis or solitary renal artery stenosis * Refractory hyperkalemia * Moderate or severe aortic stenolsis * Obstructive hypertrophic cardiomyopathy
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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