Phase 2 Lung Cancer Trial, Recruiting NCT07070440 Sponsor: Dizal Pharmaceuticals Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07070440
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:

  • You have signed a consent form agreeing to take part in the study.
  • You are 18 years of age or older.
  • You have been diagnosed with an advanced or spreading type of lung cancer (non-squamous, non-small cell) that cannot be treated with curative treatments.
  • Your lung cancer has been confirmed to have a specific gene change called an EGFR sensitizing mutation through a lab test.
  • You are able to provide tumor tissue and blood samples for additional lab testing.
  • Your cancer has stopped responding to treatment with all three generations of EGFR-targeted pills (known as EGFR TKIs).
  • You are in reasonably good general health (able to carry out normal daily activities with little or no limitation) and are expected to live at least 12 more weeks.
  • If you have cancer that has spread to the brain, any related brain surgery or radiation must have been completed at least 2 weeks before starting the trial, with side effects mostly resolved, and you must not have needed steroids or fluid-reducing medications for at least 4 weeks.
  • You have at least one area of cancer in your body that can be measured on a scan.
  • Your blood counts and organ function (such as liver and kidneys) are at acceptable levels before starting the trial.

Who may not be able to join:

  • Your lung cancer has features of, or has changed into, a different type called small cell lung cancer.
  • You received immunotherapy, antibody-based treatments, or similar cancer drugs within 4 weeks before starting the trial.
  • You received chemotherapy, other anti-cancer drugs, or experimental treatments within 14 days before starting the trial.
  • You received targeted radiation therapy within 7 days, or extensive radiation (including to large areas of bone marrow) within 28 days, before starting the trial.
  • You are currently taking — or cannot stop taking — certain medications that strongly affect how the body processes drugs (called CYP3A4 inhibitors or inducers, including some herbal supplements like St. John's Wort) within 2–3 weeks before starting the trial.
  • You are currently taking — or cannot stop taking — certain sensitive medications that interact with the study drug within 2 weeks before starting the trial (confirm with trial site).
  • You are currently taking — or cannot stop taking — proton pump inhibitors (common heartburn/acid reflux medications) within 1 week before starting the trial.
  • You have had major surgery within 4 weeks before starting the trial, or are planning major surgery during the trial.
  • You still have side effects (grade 1 or higher, apart from hair loss) from a previous cancer treatment such as chemotherapy or radiation.
  • Your cancer has spread in a way that is pressing on your spinal cord, or has spread to the membranes surrounding your brain or spinal cord.
  • You have been diagnosed with another cancer within the past 2 years (some exceptions may apply — confirm with trial site).
  • You have serious or poorly controlled conditions such as high blood pressure or a bleeding disorder.
  • You have an ongoing or active infection, including hepatitis B, hepatitis C, or HIV.
  • You have certain heart conditions or abnormalities, including irregular heart rhythms, a history of heart attack or stroke within the past 6 months, or a family history of certain heart rhythm problems (confirm with trial site).
  • You have a history of deep vein blood clots or blood clots in the lungs within 4 weeks before starting the trial.
  • You have a history of a lung condition called interstitial lung disease, or currently have active lung inflammation.
  • You have ongoing severe nausea or vomiting, a chronic gut condition, difficulty swallowing, or have had part of your intestine removed in a way that might affect how your body absorbs the study medication.
  • You have received a live vaccine within 4 weeks before starting the trial.

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 27 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: Lu, Shanghai Chest Hospital

Phone: +86 21 61095854

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
Dizal Pharmaceuticals
Registry
ClinicalTrials.gov
Start date
16 July 2025
Est. completion
1 June 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of participants with Dose-limiting Toxicities (DLTs); Number of participants with Adverse events (AEs)/Serious adverse events (SAEs); Objective Response Rate (ORR) as assessed by investigator per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

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: 27 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