Phase 2 Lung Cancer Trial, Recruiting NCT06951464 Sponsor: Sichuan University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06951464
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 willing to sign a consent form and follow the study rules
  • Adults aged 18 to 75 years old
  • People diagnosed with stage II to IIIB non-small cell lung cancer (a specific type of lung cancer) that has a particular genetic change called an EGFR-sensitive mutation, where surgery to remove the affected lung lobe is considered possible or potentially possible, and the doctor has determined that treatment before surgery is needed
  • People whose lungs are working well enough to handle surgery
  • People who have at least one tumour that can be measured on scans, according to standard research guidelines
  • People who are generally well enough to carry out daily activities with little or no limitation (as assessed by a standard medical scale)
  • People with no serious heart problems, and whose heart is pumping at a healthy level (at least 50% efficiency)
  • People whose bone marrow, liver, and kidney function all meet specific blood test thresholds set by the trial (confirm with trial site for exact values)
  • People whose blood-clotting function falls within the acceptable range set by the trial
  • People with a low level of protein in their urine, within the limits set by the trial
  • People of childbearing potential who agree to use highly effective contraception from 7 days before the first dose until 6 months after the last dose; women of childbearing potential must also have a negative pregnancy blood test within 7 days before starting treatment

Who may not be able to join:

  • People who have already received any previous treatment (systemic or local) for non-small cell lung cancer
  • People who have had another type of cancer within the past 5 years, unless it was a fully cured skin cancer, superficial bladder cancer, or certain in situ cancers (such as prostate, cervical, or breast — confirm with trial site)
  • People who have had a major surgical procedure within 4 weeks before starting the trial
  • People who currently have, or have a history of, certain types of lung inflammation (such as interstitial lung disease or radiation-related lung damage requiring steroid treatment)
  • People who have had a serious infection within 4 weeks before the screening period, such as a severe bacterial, viral, or fungal infection
  • People who have an active autoimmune disease or a history of certain autoimmune conditions (such as lupus, Crohn's disease, or Guillain-Barré syndrome); some exceptions apply, including stable thyroid conditions managed with hormone replacement and skin conditions not needing systemic treatment (confirm with trial site)
  • People who test positive for HIV, have active tuberculosis, or have an active hepatitis B or C infection
  • People with poorly controlled high blood pressure (above certain thresholds set by the trial)
  • People with a history of serious heart or brain blood vessel problems, including certain abnormal heart rhythms, heart failure, stroke, heart attack, or aortic dissection — particularly if these occurred within the past 6 months (confirm with trial site for full details)
  • People who have previously received a stem cell, bone marrow, or organ transplant from another person
  • People with a known allergy to the study drugs or any of their ingredients
  • People who have previously had any type of stem cell transplant (from themselves or another person)
  • Women who are pregnant or breastfeeding
  • People the trial doctor considers unsuitable for the trial 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 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: Yongsheng Wang, West China Hospital

Phone: 86(028)85421606

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
Sichuan University
Registry
ClinicalTrials.gov
Start date
25 June 2025
Est. completion
5 May 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological complete response (pCR); Major Pathological Response (MPR)

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