RecruitingPhase 2NCT06295432

A Phase II Clinical Trial of DZD9008 in Combination With AZD4205 in Standard Treatment Failed NSCLC Patients With EGFR Mutations (WU-KONG21)

A Phase II, Multicenter Study to Assess the Safety, Tolerability and Anti-tumor Efficacy of DZD9008 in Combination With AZD4205 in Standard Treatment Failed Non-Small Cell Lung Cancer (NSCLC) Patients With EGFR Mutations


Sponsor

Dizal Pharmaceuticals

Enrollment

90 participants

Start Date

Jun 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

DZD9008 in combination with AZD4205 for the treatment of patients with advanced NSCLC with EGFR mutations who have progressed after standard treatment. The purpose of this study is to assess the safety and efficacy of this combination therapy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (WU-KONG21) is testing a combination of two targeted drugs — DZD9008 and AZD4205 — for patients with advanced non-small cell lung cancer (NSCLC) that has a mutation in the EGFR gene (a key driver of certain lung cancers) and has stopped responding to standard treatments. **You may be eligible if...** - You are 18 or older with confirmed locally advanced or metastatic NSCLC - Your cancer has an EGFR mutation - You have received prior standard treatments that have stopped working - You are in good performance status (ECOG 0–1) with a life expectancy of at least 12 weeks - If you have brain metastases, they must be stable and previously treated **You may NOT be eligible if...** - Your lung cancer does not have an EGFR mutation - You have not yet tried standard EGFR-targeted therapies - You have active, unstable brain metastases - You have significant heart, lung, or other organ problems Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDZD9008+AZD4205

Daily dose of DZD9008+AZD4205 until intolerant, disease progression or patient decision. Starting dose of DZD9008 is 200mg once daily and starting dose of AZD4205 is 75mg once daily orally used. If tolerated, subsequent cohorts will evaluate increasing doses of the combination therapy.


Locations(4)

Guangdong Provincial People'S Hospital

Guangzhou, Guangdong, China

Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology

Wuhan, China

The First Affiliated Hospital of Xi'an Jiaotong University

Xi'an, China

Henan Cancer Hospital

Zhengzhou, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

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NCT06295432


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