Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07070440

DZD6008 Combination Therapy in Patients With Locally Advanced or Metastatic NSCLC With EGFR Mutation (TIAN-SHAN7)

A Phase 1/2, Open-Label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Anti-tumor Efficacy of DZD6008 Combination Therapy in Patients With Locally Advanced or Metastatic NSCLC With EGFR Mutation (TIAN-SHAN7)

Status
Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Dizal Pharmaceuticals · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is designed to evaluate safety and antitumor activity of DZD6008 combination therapy in patients with advanced Non-Small Cell Lung Cancer (NSCLC) with Epidermal Growth Factor Receptor (EGFR) mutations.

Conditions

Interventions

TypeNameDescription
DRUGDZD6008DZD6008 was administered orally at 40/60/90 mg QD.
DRUGPemetrexedPemetrexed 500 mg/m2, every 3 weeks, intravenous infusion.
DRUGCarboplatinCarboplatin AUC 5 mg/mL/min, every 3 weeks, intravenous infusion.
DRUGDocetaxelDocetaxel 75 mg/m2, every 3 weeks, intravenous infusion.

Timeline

Start date
2025-07-16
Primary completion
2027-06-01
Completion
2028-12-01
First posted
2025-07-17
Last updated
2025-08-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07070440. Inclusion in this directory is not an endorsement.