Phase 2 Lung Cancer Trial, Recruiting NCT07641023 Sponsor: Beijing Biotech Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07641023
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 with non-small cell lung cancer (NSCLC) that cannot be surgically removed, is at an advanced stage (Stage IIIB, IIIC, or Stage IV), and has continued to grow or spread after standard treatments — including platinum-based chemotherapy and, where appropriate, immunotherapy.
  • People whose cancer has at least one area that can be measured on scans, according to standard measurement guidelines called RECIST v1.1.
  • People who have stored tumour tissue samples available from a previous biopsy, or who are willing to have a new biopsy taken, so that the tumour can be tested for specific proteins.
  • People whose tumour shows high levels of at least two out of three specific proteins — MSLN, EGFR, and HER2/ERBB2 — based on laboratory testing at the start of the trial (confirm specific thresholds with trial site).
  • People with a good general level of physical functioning, rated 0 or 1 on a standard medical scale called the ECOG scale (meaning fully active or able to carry out light activity).
  • People whose liver, kidneys, and blood counts are working within acceptable ranges as defined by the trial's laboratory guidelines.
  • People with a life expectancy of at least 12 weeks.
  • People who are not pregnant, confirmed by a negative pregnancy test if applicable, and who agree to use effective contraception for the period required by the trial.
  • People who are able to understand the trial information and are willing to sign a written consent form.

Who may not be able to join:

  • People with brain or spinal cord involvement from their cancer that is active and not well controlled. People with previously treated and stable brain involvement may still be considered if their condition is clinically stable and they are no longer on high-dose steroid medication.
  • People who have received a type of specialised cell-based gene therapy — such as CAR-T, CAR-NK, or TCR-T therapy — within the past 3 months, or any previous treatment that the trial doctor considers may increase the risk of serious side effects.
  • People who have previously experienced a severe reaction called cytokine release syndrome (CRS) or a serious nervous system complication called ICANS from prior treatments.
  • People with significant ongoing lung inflammation or scarring (interstitial lung disease or pneumonitis) that requires steroid treatment, or other serious uncontrolled lung conditions that could make it difficult to monitor for side effects.
  • People with an active autoimmune disease that requires ongoing immune-suppressing medication (low-dose steroid replacement for hormone deficiency may be permitted — confirm with trial site).
  • People with an active, uncontrolled infection, including uncontrolled HIV, active hepatitis B, or active hepatitis C.
  • People with serious heart conditions, such as a recent heart attack, unstable chest pain, an uncontrolled irregular heartbeat, or reduced heart pumping function below the level set by the trial site.
  • People who are pregnant or breastfeeding.
  • People who are currently receiving other cancer treatments — such as chemotherapy, targeted therapy, or immunotherapy — and have not waited the required time since their last treatment as defined by the trial.
  • People with any other condition that the trial doctor believes would affect their safety or their ability to participate fully in the trial.

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 26 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 13076790030

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
Beijing Biotech
Registry
ClinicalTrials.gov
Start date
2 March 2026
Est. completion
14 March 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of dose-limiting toxicities (DLTs); Recommended Phase 2 dose (RP2D); Objective response rate (ORR) per RECIST v1.1

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: 26 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