Phase 2 Lung Cancer Trial, Recruiting NCT06352008 Sponsor: Tianjin Medical University Cancer Institute and Hospital Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06352008
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 participate, have signed a consent form, and are expected to follow the study requirements
  • People who are 18 years of age or older, of any gender, with a good general health and activity level (ECOG score 0–1), and an expected survival of at least 3 months
  • People diagnosed with stage IIA to IIIA non-small cell lung cancer (a specific type and stage of lung cancer), who previously received a combination of immune checkpoint therapy (PD-1/PD-L1 inhibitors) and chemotherapy before surgery, and who then had surgery where all visible cancer was successfully removed (called R0 resection), staged using the AJCC/UICC 8th edition lung cancer staging system
  • People whose cancer did not fully disappear after the pre-surgery treatment (i.e., did not achieve a pathological complete response), and who are between 4 and 12 weeks past their surgery at the time of receiving the first study treatment
  • People whose major organs (such as heart, liver, and kidneys) are functioning well enough to meet the study's health standards
  • Women of childbearing age who agree to use effective contraception during the study and for 6 months afterward, and who have a negative pregnancy test within 7 days before joining; men who agree to use effective contraception during the study and for 6 months afterward

Who may not be able to join:

  • People who have had, or currently have, another type of cancer within the past 5 years — with two exceptions: cancers that were fully treated with a single surgery and have been free of disease for 5 continuous years, or certain low-risk, cured cancers such as early-stage cervical cancer in situ, non-melanoma skin cancers, or certain superficial bladder cancers
  • People whose cancer has a known genetic change (mutation) for which targeted drug treatments have already been approved — people with non-squamous cell lung cancer are required to have had EGFR or ALK gene testing done or to provide previous test results
  • People with certain heart or blood vessel conditions, including: a history of heart failure or significant heart rhythm blockage (Grade II or higher); a past or current heart attack or unstable chest pain, or irregular heart rhythms requiring treatment; or a blood clot or stroke-related event (such as a mini-stroke, brain bleed, brain infarction, deep vein clot, arterial clot, or pulmonary embolism) within the past 6 months
  • People who have participated in another clinical drug trial within the past 30 days
  • People who have taken certain traditional Chinese medicines with anti-tumour indications (as listed in China's NMPA-approved drug instructions) within the 2 weeks before starting the study treatment
  • People who have had a major surgical procedure (other than the lung cancer removal surgery) within the 4 weeks before starting the study treatment, or who the investigating doctor determines are not suitable for the study for other reasons

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: 008618526812877

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 July 2024
Est. completion
1 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Event-Free Survival (EFS)

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