Phase 2 Lung Cancer Trial, Recruiting NCT06114225 Sponsor: Ruijin Hospital Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06114225
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:

  • You have signed a written consent form before any trial procedures begin.
  • You have been diagnosed with osteosarcoma (a type of bone cancer) that has spread to the lungs, confirmed by a tissue biopsy, and you do not currently have the cancer returning at the original bone site (though previous surgery to remove a local recurrence with clear margins is allowed).
  • The spots on your lungs can be surgically removed by taking out a small portion of lung tissue, and there is no cancerous fluid around your lungs.
  • You have already received at least one standard cancer treatment, and you have never previously been treated with a drug called gemcitabine.
  • Your lungs are healthy enough to undergo one or two surgeries on your chest.
  • You are between 10 and 65 years old.
  • If you are 16 or older, your general physical ability and daily functioning falls within an acceptable range on a standard medical scale (including people with amputations who can mostly care for themselves and move around more than half of their waking hours with aids such as a walker or wheelchair).
  • If you are under 16, your ability to carry out daily activities meets a minimum acceptable level on a scale used for children (including children with amputations who can still take part in most activities with the help of a walker or wheelchair).
  • Your doctors expect you to live for more than 24 weeks.
  • Most of your returning cancer spots can be treated with a focused type of radiation therapy called SBRT (stereotactic body radiotherapy).
  • Your major organs (such as heart, liver, and kidneys) are working at a safe enough level, as confirmed by tests done 7–14 days before treatment starts.
  • If you are a woman who could become pregnant, you agree to use reliable contraception during the study and for 6 months afterward, you have tested negative for pregnancy within 7 days of starting the study, and you are not currently breastfeeding; if you are male, you agree to use contraception during the study and for 6 months afterward.
  • If you have spots on your lungs that were previously treated with surgery, a heat-based procedure (radiofrequency ablation), or radiation, you may still be eligible depending on whether those spots have stayed stable or grown — the trial team will assess this on a case-by-case basis (confirm with trial site).

Who may not be able to join:

  • You have been diagnosed with another cancer (other than the one being studied) within the past 5 years.
  • You are currently taking part in another clinical trial, or you have received an experimental drug or used experimental medical equipment within the past 4 weeks.
  • You have previously been treated with certain types of immunotherapy drugs (such as anti-PD-1, anti-PD-L1, anti-PD-L2, or similar immune-targeting drugs), and your cancer eventually stopped responding to that treatment after initially working.
  • You have taken certain Chinese herbal medicines with anti-cancer effects, or drugs that affect the immune system (such as thymosin, interferon, or interleukin), within the past 2 weeks — except when used locally to treat fluid around the lungs.
  • You have had an active autoimmune disease (where your immune system attacks your own body) requiring ongoing medical treatment within the past 2 years — note that simple hormone replacement therapies are not counted as exclusions.
  • You are currently taking steroid tablets or injections, or other medicines that suppress your immune system, within 7 days before starting the trial (steroid nasal sprays, inhalers, or creams are not counted).
  • You have previously had an organ transplant from another person (except a cornea transplant), or a stem cell transplant from another person.
  • You have a known severe allergy (grade 3 or higher) to any ingredient in monoclonal antibody medicines.
  • You have not yet fully recovered from side effects of any previous cancer treatment (confirm with trial site).
  • You are known to be HIV-positive.
  • You have received a live vaccine within the past 30 days before starting the trial.
  • You are currently pregnant or breastfeeding.
  • You have any serious or uncontrolled illness affecting your whole body (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 21 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: Weibin Zhang, PhD, MD, Ruijin Hospital

Phone: +8613501824630

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
Registry
ClinicalTrials.gov
Start date
1 June 2023
Est. completion
15 September 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

12-month progression-free survival rate (12m-PFSR)

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: 21 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