Phase 2 Lung Cancer Trial, Recruiting NCT05266846 Sponsor: Hunan Province Tumor Hospital Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT05266846
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 are 18 years of age or older at the time of signing the consent form
  • People who have been diagnosed with stage IV lung adenocarcinoma (a type of lung cancer) that has a specific genetic change called an ALK rearrangement, and whose cancer has continued to grow after treatment with a medicine called alectinib as the first treatment
  • People who have at least one area of cancer in the body that can be measured on a scan, as determined by the trial site's medical team (areas that have previously been treated with radiation therapy for pain relief cannot be used as the measured target)
  • People who have 20 prepared tissue samples from a previous biopsy available; those who do not have suitable tissue samples on file will need to have a new biopsy performed to provide a tissue sample
  • People whose physical ability and daily functioning is rated at 0 or 1 on a standard scale used by doctors (meaning they are either fully active or have minor limitations but can carry out light activity)
  • People with a life expectancy of at least 3 months
  • People with adequate blood counts and organ function, as determined by the trial site (confirm with trial site)

Who may not be able to join:

  • People who have cancer that has spread to the brain or spinal cord that is either currently active or has not yet been treated
  • People who have had a different cancer (other than the type of lung cancer this trial focuses on) within the past 5 years, unless that cancer carried very little risk of spreading or causing death and was treated with the intention of a cure
  • People who are pregnant or currently breastfeeding
  • People who have an active autoimmune disease (where the immune system attacks the body) that has required medication to treat it at any point in the past 2 years
  • People who have a history of certain lung conditions, including idiopathic pulmonary fibrosis, organising pneumonia, drug-induced lung inflammation, or unexplained lung inflammation — or who show signs of active lung inflammation on a chest scan at the time of screening (a history of scarring from radiation in a treated area is acceptable)
  • People who have tested positive for HIV
  • People who have active hepatitis B or hepatitis C infection
  • People who have had a serious infection within the 4 weeks before joining the trial
  • People who have significant heart or cardiovascular disease (confirm with trial site for specific conditions)
  • People who have an illness or condition that would prevent them from understanding or following the trial procedures
  • People who are currently taking part in another clinical trial involving an experimental treatment, or who have received an experimental treatment or used an experimental medical device within 4 weeks before the first dose in this trial
  • People who have previously been treated with certain types of immunotherapy medicines known as anti-PD-1 or anti-PD-L1 antibodies, or with medicines that target a protein called VEGF

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 23 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: Yongchang C Zhang, MD, Hunan Cancer Hospital

Phone: +8613873123436

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
Hunan Province Tumor Hospital
Registry
ClinicalTrials.gov
Start date
29 May 2024
Est. completion
16 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

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: 23 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