Phase 3 Lung Cancer Trial, Recruiting NCT06417008 Sponsor: Hansoh BioMedical R&D Company Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT06417008
Recruiting Phase 3

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 are between 18 and 75 years old (inclusive)
  • You have been newly diagnosed with a specific type of lung cancer (non-small cell lung cancer, or NSCLC) that has spread locally or to other parts of the body (stage IIIB, IIIC, or IV), has a specific genetic change called an EGFR-sensitive mutation, and has not yet been treated
  • Your cancer cannot be treated with surgery or radiation with curative intent
  • You are willing to provide a tumor tissue sample, either previously collected or newly obtained
  • You have at least one measurable tumor that can be tracked during the study
  • You are generally able to carry out daily activities with little to no limitation (confirm with trial site for exact fitness level required)
  • Your doctors estimate you have a life expectancy of more than 12 weeks
  • You are willing and able to use reliable contraception throughout the study
  • You are not pregnant at the time of screening (if applicable)
  • You have read and signed the informed consent form agreeing to take part

Who may not be able to join:

  • You have previously received or are currently receiving treatments targeting MET or EGFR, including certain antibody-based therapies
  • You have had major surgery, certain traditional Chinese herbal medicines for cancer, or other local treatments too recently before the study starts
  • You have a build-up of fluid around your lungs, abdomen, or heart that requires medical treatment
  • You have recently taken certain other experimental drugs, strong medications that affect how the body processes drugs, or medications known to affect heart rhythm (confirm with trial site for exact timing)
  • You are still experiencing significant side effects (Grade 2 or higher) from a previous cancer treatment
  • You have a history of another type of cancer (other than the one being studied)
  • You have cancer that has spread to the brain or spinal cord that is untreated or currently active
  • Your blood counts or organ function (such as liver or kidneys) are not at an adequate level
  • You have a serious, uncontrolled, or active heart or blood vessel condition
  • You have a serious or uncontrolled illness affecting your overall health
  • You have serious bleeding problems or a tendency to bleed
  • You have had a serious blood clot in a vein or artery
  • You have a serious or active infection
  • You have an active infectious disease (confirm with trial site for specifics)
  • You have a lung condition called interstitial lung disease (ILD)
  • You have a serious neurological or mental health condition
  • You have had a severe allergic reaction to any of the study drugs or similar medicines in the past
  • You are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study or within 6 months after the last dose
  • You have a history of severe allergic reactions or severe reactions to infused medications
  • You have any other condition that the study doctor believes could put you at risk or affect the study results

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 3: approximately ~65% 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: Dingzhi Huang, M.D., Tianjin Medical University Cancer Institute and Hospital

Phone: +86 18652105685

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 3
Sponsor
Hansoh BioMedical R&D Company
Registry
ClinicalTrials.gov
Start date
28 May 2024
Est. completion
1 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

[Phase Ib] Objective response rate (ORR) According to response evaluation criteria in solid tumors (RECIST) v1.1 by Investigators (INVs); [Phase III] Progression-Free Survival (PFS) According to RECIST v1.1 by Independent Review Committee(IRC)

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