Phase 2 Lung Cancer Trial, Recruiting NCT06256237 Sponsor: Shanghai Pulmonary Hospital, Shanghai, China Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06256237
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 and able to sign a consent form agreeing to take part in the study.
  • People aged 18 years or older.
  • People who have been diagnosed with small cell lung cancer (SCLC) through a tissue or cell sample, and whose cancer has been confirmed as limited stage (not spread widely) through imaging scans such as CT or PET-CT.
  • People with a good general level of physical functioning, rated 0 or 1 on a standard medical scale (meaning largely able to carry out daily activities with little or no restriction).
  • People with a life expectancy of at least 12 weeks.
  • People who have at least one measurable tumour as assessed by standard imaging criteria.
  • People whose liver, kidneys, and blood system are functioning well enough to participate.
  • People whose cancer has not spread to other parts of the body.
  • People whose cancer is expected to be able to be completely removed by surgery.
  • People whose lung function is strong enough to tolerate a surgical procedure.
  • Women who are able to become pregnant must use effective contraception throughout the study and for at least 120 days after the last chemotherapy or last dose of the study drug (whichever comes later), and must have a negative pregnancy test within 7 days before joining.
  • Men who have not had a sterilisation procedure must use effective contraception throughout the study and for at least 120 days after the last chemotherapy or last dose of the study drug (whichever comes later).

Who may not be able to join:

  • People who have previously received any cancer treatment for a thymic epithelial tumour, including surgery, radiation, chemotherapy, targeted therapy, or experimental treatment.
  • People who have had a different type of cancer (other than SCLC) within the five years before the start of this trial.
  • People with serious or unstable health conditions, including active infection, uncontrolled high blood pressure, recent or ongoing chest pain (angina), moderate-to-severe heart failure, a heart attack within the past six months, serious irregular heartbeat requiring medication, or significant liver, kidney, or metabolic disease.
  • People with an active or suspected autoimmune disease, or a nerve or muscle condition related to cancer affecting the immune system, that requires ongoing systemic treatment.
  • People who have a known allergy to the study drug or any of its ingredients.
  • People who currently have interstitial lung disease (a condition causing scarring or inflammation in the lungs).
  • People with active hepatitis B, hepatitis C, or HIV.
  • People who are pregnant or currently breastfeeding.
  • People who have difficulty absorbing food or nutrients normally (confirm with trial site).
  • People with neurological or psychiatric conditions that would make it difficult to cooperate with the study.
  • People whom the trial investigators consider unsuitable 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 13 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: 02165115006

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
Shanghai Pulmonary Hospital, Shanghai, China
Registry
ClinicalTrials.gov
Start date
1 April 2024
Est. completion
31 January 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathologic complete response (PCR) rate

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: 13 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