Phase 3 Lung Cancer Trial, Recruiting NCT05211895 Sponsor: AstraZeneca Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT05211895
Recruiting Phase 3

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:

  • People who are 18 years of age or older at the time of screening
  • People who have been diagnosed with non-small cell lung cancer (a specific type of lung cancer), confirmed through a tissue or cell sample, and who have been treated with a combined chemotherapy and radiation therapy (given at the same time) for stage III lung cancer that cannot be surgically removed
  • People who can provide a tumour tissue sample that was collected before their chemotherapy and radiation treatment
  • People whose tumour tests positive for a protein called PD-L1 at a level of 1% or higher, confirmed by a central laboratory
  • People whose tumour tests negative for certain gene changes known as EGFR and ALK mutations
  • People whose cancer has not grown or spread after completing their chemotherapy and radiation treatment
  • People who received at least 2 rounds (cycles) of platinum-based chemotherapy at the same time as their radiation therapy
  • People who received a total radiation dose of between 54 and 66 Gray (a unit used to measure radiation) as part of their treatment
  • People who are in good general health, rated as 0 or 1 on a standard medical fitness scale (meaning fully active or able to carry out light activity)
  • People whose organs (such as kidneys, liver, and bone marrow) are functioning well enough as shown by blood tests

Who may not be able to join:

  • People who have had another type of cancer in the past, unless it was fully treated with no signs of return and has not required active treatment in the last 3 years, or it was a certain low-risk skin cancer or an early-stage non-invasive cancer with no current signs of disease
  • People whose lung cancer is a mixed type involving both small cell and non-small cell lung cancer
  • People who received their chemotherapy and radiation therapy separately (one after the other) rather than at the same time
  • People whose lung cancer got worse or spread during their combined chemotherapy and radiation treatment
  • People who still have significant side effects (above a moderate level) from their previous chemotherapy and radiation treatment, other than hair loss
  • People who developed moderate or severe lung inflammation (pneumonitis) as a result of their previous treatment
  • People who have a history of certain lung scarring or inflammation conditions, or who currently have active lung inflammation, active lung infection, active fluid around the lungs, or ongoing lung scarring — regardless of cause
  • People who have or have had active autoimmune or inflammatory conditions (diseases where the immune system attacks the body), with some exceptions (confirm with trial site)
  • People who have an active infection with a virus called Epstein-Barr virus (EBV), or are suspected of having a long-term active EBV infection
  • People who have used medications that suppress the immune system within 14 days before starting the study drug

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
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Hidehito Horinouchi, MD, PhD, National Cancer Center Hospital

Phone: 1-877-240-9479

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
18 February 2022
Est. completion
12 July 2028

Where this trial is recruiting

🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇱 Chile 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece Hong Kong 🇭🇺 Hungary 🇮🇳 India 🇮🇹 Italy 🇯🇵 Japan 🇲🇾 Malaysia 🇲🇽 Mexico 🇳🇴 Norway 🇵🇭 Philippines 🇵🇱 Poland 🇷🇴 Romania 🇿🇦 South Africa 🇰🇷 South Korea 🇪🇸 Spain 🇨🇭 Switzerland 🇹🇼 Taiwan 🇹🇭 Thailand Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States 🇻🇳 Vietnam

Primary endpoints

Progression Free Survival (PFS)

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