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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT04878016

NCT04878016
Completed Phase 3

Who may be able to join

Who might be able to join this trial:

  • You are 18 years of age or older (any gender)
  • You have been diagnosed with Small Cell Lung Cancer (SCLC) confirmed by a tissue or cell sample test
  • Your SCLC is at an advanced (extensive) stage, meaning it has spread significantly
  • You have not yet received any first-line (initial) treatment for your advanced SCLC
  • If you had previous surgery or treatments aimed at curing an earlier cancer, at least 6 months must have passed since your last chemotherapy or radiation before your advanced SCLC was diagnosed
  • You are generally able to carry out daily activities with little to no limitation (your doctor will assess this)
  • Your doctors estimate you are likely to survive at least 8 weeks
  • A CT or MRI scan taken within the last 28 days shows at least one measurable tumor
  • You are willing and able to use effective contraception for the duration of the study and for 6 months after the last dose; women of childbearing age must have a negative pregnancy test within 7 days before starting treatment
  • Your blood, liver, kidney, and clotting function results meet specific healthy ranges before starting treatment (your doctor will check these with blood tests)
  • You are able to provide a tumor tissue sample within about 4 weeks of joining, so researchers can test it for a protein called PD-L1
  • You are willing to give your informed consent, follow the study requirements, and attend follow-up appointments

Who may not be able to join:

  • You have previously been treated with certain types of immune therapy drugs, such as checkpoint inhibitors (e.g. PD-1, PD-L1, or CTLA-4 blockers), or anti-blood vessel growth (anti-VEGF/VEGFR) treatments
  • You currently have active cancer spread to the brain or the lining around the brain that has not been treated — treated brain metastases may be acceptable if certain conditions are met (confirm with trial site)
  • You had radiation therapy to the brain or bones fewer than 7 days before starting the study drug
  • You have an active autoimmune disease (a condition where your immune system attacks your own body), such as lupus, rheumatoid arthritis, multiple sclerosis, or inflammatory bowel disease — some well-controlled conditions like thyroid disease or type 1 diabetes may still be eligible (confirm with trial site)
  • You have fluid build-up in your chest, around your heart, or in your abdomen that needs to be drained regularly (more than once a month), unless you have a permanent drainage tube in place
  • You have taken steroid medications (above a low dose) or other immune-suppressing drugs within the 14 days before starting the study — some exceptions may apply (confirm with trial site)
  • You have received or are planning to receive a live vaccine within 4 weeks before starting the study drug
  • You have had major surgery within 4 weeks before starting the study, or major surgery is planned during the study
  • You have a lung condition called interstitial lung disease, drug-related lung inflammation, or radiation-related lung inflammation that requires steroid treatment, or you have active pneumonia with symptoms
  • You have active tuberculosis or had active tuberculosis within the past year
  • You have serious uncontrolled heart problems, such as significant heart failure, unstable chest pain, a heart attack or stroke within the last 6 months, or serious heart rhythm problems needing treatment
  • You have an active, uncontrolled infection currently requiring intravenous (IV) antibiotics, antifungals, or antiviral treatment
  • You have active hepatitis B, active hepatitis C (unless virus levels are undetectable after treatment), or are HIV-positive or have AIDS — some exceptions may apply (confirm with trial site)
  • You have a known allergy to the study drugs or their ingredients, or a history of severe reactions to any similar antibody-based treatment, or allergies to carboplatin or etoposide
  • You have previously had a bone marrow transplant or an organ transplant from another person
  • You have had another type of cancer within the last 5 years — some fully treated, low-risk cancers (such as certain skin cancers or early-stage prostate cancer) may be exceptions (confirm with trial site)
  • You have taken part in another experimental drug trial within 4 weeks before signing up for this study
  • You are currently pregnant

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

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.

Trial details

Status
Completed
Phase
Phase 3
Sponsor
Lee's Pharmaceutical Limited
Registry
clinicaltrials_gov
Start date
15 July 2021
Est. completion
13 October 2023

Where this trial is recruiting

🇨🇳 China

Primary endpoints

overall survival

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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov