Phase 2 Lung Cancer Trial, Recruiting NCT06667622 Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences Condition: Lung Cancer
Back to Lung Cancer

Phase 2 Lung Cancer Trial, Recruiting

NCT06667622
Recruiting Phase 2

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 have been diagnosed with non-small cell lung cancer, confirmed through a tissue or cell sample.
  • People with stage II or stage III non-small cell lung cancer that cannot be removed by surgery, and who have already received treatment before surgery (neoadjuvant therapy).
  • People with a general health and activity level rated as 0, 1, or 2 on a standard medical scale (meaning able to carry out daily activities with little to no limitations).
  • People whose organs (such as liver and kidneys) and bone marrow are functioning at an adequate level.

Who may not be able to join:

  • People who have had radiotherapy in the past.
  • People who have experienced immune-related lung inflammation (pneumonitis) rated at grade 2 or higher during previous treatment.
  • People whose cancer in a specific area still requires surgery.
  • People who have had another separate primary cancer at some point.
  • People with a history of an active primary immune system deficiency condition.
  • People whose tissue samples show a mixed type of cancer containing both small cell and non-small cell lung cancer.
  • People who are still experiencing side effects from chemotherapy or radiotherapy received before the study that have not been resolved (confirm with trial site).

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 2: approximately ~30% 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: Lei Deng, MD, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: 010-87787692

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 2
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Registry
ClinicalTrials.gov
Start date
29 May 2024
Est. completion
10 January 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence and severity of grade 3 and above radiation esophagitis; Incidence and severity of grade 2 and above radiation pneumonitis

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