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
| Type | Name | Description |
|---|---|---|
| DRUG | DZD6008 | DZD6008 was administered orally at 40/60/90 mg QD. |
| DRUG | Pemetrexed | Pemetrexed 500 mg/m2, every 3 weeks, intravenous infusion. |
| DRUG | Carboplatin | Carboplatin AUC 5 mg/mL/min, every 3 weeks, intravenous infusion. |
| DRUG | Docetaxel | Docetaxel 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.