Phase 3 Lung Cancer Trial, Recruiting NCT07050043 Sponsor: Dr Arvindran A/L Alaga Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT07050043
Recruiting Phase 3

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:

  • You are 18 years of age or older
  • You have been diagnosed with a type of lung cancer called non-small cell lung cancer (NSCLC) — either squamous or non-squamous — that is advanced or has spread to other parts of the body (stage IIIB–IV), confirmed by a tissue test, and has not been treated yet for this advanced stage
  • Your cancer has been tested and shows a result for a protein called PD-L1, and surgery or combined chemotherapy-radiation treatment aimed at curing the disease is not an option for you
  • If you had treatment in the past for an earlier stage of the same cancer, that treatment must have finished at least 6 months before starting this trial
  • You are generally well enough to carry out light daily activities (your doctor will assess this using a standard scale called ECOG, scored 0 or 1)
  • You have at least one measurable tumor that can be tracked on scans
  • Your blood tests show that your heart, liver, kidneys, and other organs are working well enough (specific values will be checked at your screening visit)
  • If cancer has spread to your brain, it must be stable, not causing symptoms, already treated, and you must not have needed steroid medication for it for at least 2 weeks before starting the trial
  • You are able to provide a tumor tissue sample — either from stored tissue or a new biopsy
  • If you are male, you agree to use contraception from the first dose until at least 90 days after the last dose, and not to donate sperm during this time
  • If you are a woman who could become pregnant, you are not currently pregnant or breastfeeding, and you agree to use contraception throughout the treatment period and for at least 180 days after the last dose

Who may not be able to join:

  • Your lung cancer has specific genetic changes known as EGFR, ALK, or ROS1 mutations
  • You have advanced (locally advanced) disease but could still receive other treatments that might cure it, such as access to approved immunotherapy
  • You have previously been treated with certain immune-based drugs that target PD-1, PD-L1, or similar immune checkpoint proteins
  • You have received a live vaccine (for example, for flu or other infections) within 28 days before starting the trial
  • You have certain serious underlying health conditions that could make the trial treatment unsafe — such as a history of lung inflammation (interstitial lung disease or pneumonitis), or a current serious infection requiring IV antibiotics or antifungals within 14 days of starting treatment (confirm with trial site)
  • You currently need high doses of steroid medications (more than 10 mg/day of prednisone or equivalent) or other medicines that suppress the immune system
  • You currently have active hepatitis B, hepatitis C, or HIV infection
  • You have a known allergy or sensitivity to any ingredient in the trial medicines
  • You have a known history of an autoimmune disease and are currently taking medicines to suppress your immune system
  • You have been diagnosed with another cancer within the past two years
  • Your expected survival is three months or less
  • If you are a woman who could become pregnant, a pregnancy test taken within 72 hours before starting treatment must be negative

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 12 July 2026
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.
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: Dr. Arvindran A/L Alaga, Hospital Sultanah Bahiyah

Phone: +6047407395

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 3
Sponsor
Dr Arvindran A/L Alaga
Registry
ClinicalTrials.gov
Start date
19 May 2025
Est. completion
31 December 2030

Where this trial is recruiting

🇲🇾 Malaysia

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: 12 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