Lung Cancer Trial, Recruiting NCT06717243 Sponsor: Oncology Center of Biochemical Education And Research Condition: Lung Cancer
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Lung Cancer Trial, Recruiting

NCT06717243
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults between 18 and 85 years of age.
  • People who have been diagnosed with locally advanced extensive-stage small cell lung cancer (ES-SCLC), confirmed by a tissue sample (biopsy).
  • People who have been diagnosed with locally advanced or metastatic large cell neuroendocrine carcinoma (LCNEC), confirmed by a tissue sample (biopsy).
  • People who are about to begin a standard treatment plan combining platinum-based chemotherapy (cisplatin or carboplatin) with an immunotherapy drug (atezolizumab or durvalumab).
  • People who have at least one tumour that can be measured or tracked using standard imaging guidelines (called RECIST 1.1).
  • People who have not previously received any systemic (whole-body) treatment for ES-SCLC or LCNEC.
  • People whose treating doctor estimates their life expectancy to be at least 3 months.
  • People who are willing to attend scheduled follow-up visits and provide blood and/or tissue samples during the study.
  • People with a physical functioning level rated 0–2 on the ECOG scale, meaning they are able to carry out at least some daily activities (confirm with trial site).
  • People whose blood counts, kidney function, and liver function are considered adequate by their treating doctor.
  • People who are willing and able to sign a written consent form and provide blood and tumour tissue samples for research.
  • Women of childbearing potential who have a negative pregnancy test at the start of the study and agree to use effective contraception throughout.
  • People who do not have medical conditions that would prevent them from safely receiving immunotherapy drugs (such as certain autoimmune diseases requiring immune-suppressing medication).
  • People who their treating doctor considers medically fit to receive platinum-based chemotherapy.
  • People with brain metastases (cancer that has spread to the brain) may still be eligible if those metastases have already been treated (for example, with surgery or radiotherapy) and have been stable on imaging for at least 4 weeks before joining the trial.
  • People with brain metastases who are taking corticosteroid medication may still be eligible if their dose is stable or decreasing and is no more than the equivalent of 10 mg per day of prednisone for at least 2 weeks before joining.
  • People who have adequate psychosocial support and the mental capacity to understand and consent to participation.

Who may not be able to join:

  • People with untreated or worsening brain metastases that are causing significant neurological symptoms.
  • People who have had another active cancer (other than ES-SCLC or LCNEC) within the past 3 years, except for certain treated skin cancers or early-stage cervical cancer that has been treated.
  • People who have previously received chemotherapy or immunotherapy for ES-SCLC or LCNEC.
  • People with serious ongoing health conditions — such as uncontrolled heart, lung, or autoimmune disease — that could affect their ability to participate or receive treatment.
  • People with active infections that require systemic (whole-body) treatment, including tuberculosis, hepatitis B, hepatitis C, or HIV.
  • Women who are pregnant or breastfeeding, or women of childbearing potential who are not using effective contraception.
  • People who are taking immune-suppressing medications, including high-dose corticosteroids (more than the equivalent of 10 mg per day of prednisone), within 2 weeks before joining the trial.
  • People who have had a severe allergic reaction to any component of the planned treatment, including platinum-based chemotherapy or immunotherapy drugs.
  • People whose treating doctor estimates their life expectancy to be less than 3 months.
  • People who are unable or unwilling to follow the study procedures, including providing samples and attending follow-up visits.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Oncology Center of Biochemical Education And Research
Registry
ClinicalTrials.gov
Start date
20 February 2025
Est. completion
20 March 2028

Where this trial is recruiting

🇬🇷 Greece 🇺🇸 United States

Primary endpoints

Number of Participants with Genomic and Epigenetic Alterations Associated with Resistance to Chemo-Immunotherapy

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov