Phase 2 Lung Cancer Trial, Recruiting NCT07358676 Sponsor: Tianjin Medical University Cancer Institute and Hospital Condition: Lung Cancer
Back to Lung Cancer

Phase 2 Lung Cancer Trial, Recruiting

NCT07358676
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 have been diagnosed with extensive-stage small cell lung cancer (a type of lung cancer that has spread), confirmed through a tissue or cell sample.
  • People who have not yet received any systemic (whole-body) treatment for this type of lung cancer.
  • People who have at least one tumour that can be measured on a scan, according to standard research measurement guidelines.
  • People aged between 18 and 75 years.
  • People whose general physical health and ability to carry out daily activities falls within a certain acceptable range, as assessed by a doctor using a standard scale (confirm with trial site).
  • People who are expected to live for at least 3 months.
  • People whose blood cell counts, kidney, liver, heart, and clotting functions all meet minimum levels set by the trial (confirm with trial site for the specific values).
  • Women who could become pregnant must have a negative pregnancy test within 3 days before starting treatment and must agree to use highly effective contraception throughout the trial.
  • Men must agree to use barrier contraception (such as condoms) during the trial.
  • People who are willing and able to sign a consent form and follow the study procedures.

Who may not be able to join:

  • People who have brain metastases (cancer that has spread to the brain) that are causing symptoms. Those with treated, stable, symptom-free brain metastases for at least one month without the need for steroids may still be considered.
  • People who have previously had radiotherapy to the chest area for small cell lung cancer.
  • People who have previously been treated with certain types of cancer medicines, including anti-angiogenic drugs (such as anlotinib or bevacizumab) or immune checkpoint therapies targeting PD-1 or PD-L1.
  • People who have difficulty swallowing or have had major bowel or stomach surgery that could affect the ability to take oral (swallowed) medication.
  • People who have fluid build-up around the lungs, heart, or abdomen that is not under control and requires repeated draining.
  • People whose scans show that the tumour is growing into major blood vessels, or who are considered at high risk of serious bleeding by the treating doctor.
  • People with a history of significant bleeding problems, including coughing up more than roughly one tablespoon of blood per day in the past 3 months, or any significant bleeding episode within 4 weeks before joining the trial.
  • People who have had major surgery, an open biopsy, or a serious injury within 28 days before joining the trial.
  • People who have had a blood clot or stroke (in an artery or vein) within the past 6 months, such as a stroke, deep vein thrombosis, or pulmonary embolism.
  • People who have an active autoimmune disease that has required systemic (whole-body) treatment at any point in the 2 years before starting the trial.
  • People who have any other medical condition that the treating doctor believes would increase risk or make participation in the trial unsuitable.

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 20 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: Dingzhi Huang, Doctor, Tianjin Medical University Cancer Institute and Hospital

Phone: 86-22-23340123

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
Tianjin Medical University Cancer Institute and Hospital
Registry
ClinicalTrials.gov
Start date
1 February 2026
Est. completion
1 January 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-Free Survival (PFS)

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: 20 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