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Pill form chemo shows promise for older lung cancer patients in new trial

NCT ID NCT07599163

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests an oral chemotherapy (paclitaxel) combined with immunotherapy given before surgery in patients aged 70-85 with non-small cell lung cancer. The goal is to see if this approach can shrink tumors enough to improve surgery outcomes and long-term survival. About 75 participants will receive the treatment, and researchers will monitor side effects and how well the cancer responds.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 75 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2030

An estimate. End dates often move.

Lead sponsor

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

70 to 85 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Eligibility Criteria Inclusion Criteria: * Age 70-85 years, any gender * ECOG performance status 0-1 * Pathologically confirmed non-small cell lung cancer (NSCLC), clinical stage IIA-IIIB (8th edition AJCC) * No distant metastasis, deemed resectable with curative intent * Negative for sensitive driver mutations including EGFR, ALK, and ROS1 by molecular pathology * Adequate function of major organs, defined as: * Bone marrow: ANC ≥1.5×10⁹/L, platelet ≥100×10⁹/L, hemoglobin ≥9 g/dL * Liver function: total bilirubin ≤1.5×ULN; ALT, AST ≤2.5×ULN * Renal function: serum creatinine ≤1.5×ULN or creatinine clearance ≥60 mL/min; urine protein \< +; if +, 24-h urine protein \< 500 mg * Normal blood glucose or well-controlled diabetes * Pulmonary function: baseline FEV1 ≥2 L; if FEV1 \< 2 L, postoperative predicted FEV1 \> 800 mL confirmed by surgical evaluation * Cardiac function: no myocardial infarction, unstable angina, severe arrhythmia, or cardiac insufficiency within the past 1 year * Patients and families are fully informed and voluntarily provide written informed consent Exclusion Criteria: * Previous lobectomy, radiotherapy, or systemic antitumor therapy * Synchronous other malignancy with \<5 years of cure (except carcinoma in situ of the cervix, basal cell or squamous cell carcinoma of the skin) * History of active autoimmune disease or requirement for systemic immunosuppressive therapy * Active infection requiring systemic therapy, including active tuberculosis, HIV infection, chronic hepatitis B/C with active replication, or syphilis * Severe cardiac, hepatic, renal, or metabolic disease that cannot tolerate surgery or study treatment * Previous interstitial lung disease, drug-induced pneumonitis, or radiologic evidence of active interstitial lung disease * Uncontrolled massive pleural effusion or pericardial effusion * Major surgery, severe trauma, or other investigational drug therapy within 4 weeks * Recent vaccination with antitumor vaccines or live vaccines * Other conditions deemed inappropriate for enrollment or likely to affect trial outcomes by the investigator

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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

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  1. The official record

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