Phase 2 Lung Cancer Trial, Recruiting NCT07109401 Sponsor: Fudan University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07109401
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 able to give written consent and agree to follow the study schedule and requirements
  • People aged 18 to 75 years at the time of signing the consent form
  • People who have been confirmed through laboratory testing (tissue or cell samples) to have small cell lung cancer
  • People with limited-stage disease (a specific stage range assessed through scans and procedures such as PET-CT, bronchoscopy, or biopsy) where the treating surgeon considers the tumour removable with the goal of no cancer cells left behind — this includes certain tumour sizes and lymph node involvement, but excludes tumours that have grown into surrounding structures such as the heart, windpipe, or spine, and excludes more than one lymph node station being affected (confirm with trial site)
  • People who have not previously received any radiotherapy, chemotherapy, immunotherapy, surgery, or other systemic cancer treatments
  • People with a performance status score of 0 or 1 on the ECOG scale, meaning they are fully active or have only minor limitations in physical activity (confirm with trial site)
  • People whose life expectancy is greater than 3 months
  • People whose blood counts and organ function are within an acceptable range within 30 days before joining, as required to safely receive platinum-based chemotherapy
  • People without any medical reasons preventing them from receiving immunotherapy

Who may not be able to join:

  • People whose tumour testing shows a different type of lung cancer called non-small cell lung cancer (NSCLC)
  • People who have cancer that has spread to the brain, whether currently active or previously treated but now considered inactive
  • People who have a history of, currently have, or show signs of interstitial lung disease (a group of conditions involving scarring or inflammation of the lungs), including pulmonary fibrosis or radiation-related lung inflammation
  • People who have been taking steroid medications (corticosteroids) systemically within 14 days before the first study treatment
  • People who have previously received radiotherapy, chemotherapy, immunotherapy, surgery, or other systemic cancer treatments
  • People who have had any other active cancer within the 2 years before joining
  • People who are pregnant, breastfeeding, or planning to become pregnant during the study
  • People with serious or uncontrolled heart or blood vessel disease at the time of joining
  • People who have or have had active autoimmune or inflammatory diseases
  • People with a history of primary immune system deficiency disorders
  • People with a current active infection
  • People who have had active bleeding problems within 6 months before starting the study treatment, including vomiting blood, severe coughing up of blood, or blood in the stool
  • People with wounds that are not healing, active stomach ulcers, or bone fractures
  • People whom the trial doctor considers unsuitable for participation for any other reason

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 19 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

Phone: +86-18121299888

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
Registry
ClinicalTrials.gov
Start date
1 March 2025
Est. completion
31 March 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

One-year Event-free Survival Rate (1-year EFS Rate)

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: 19 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