An Open Label, Multicenter, Phase I/IIB Study of Dacomitinib Plus Anlotinib for Advanced Non-Small Cell Lung Cancer (NSCLC) Harboring Epidermal Growth Factor Receptor (EGFR) 21-L858R Mutations.

Who is this study for? Patients with advanced non-small cell lung cancer harboring epidermal growth factor receptor 21-L858R mutations
What treatments are being studied? Dacomitinib+Anlotinib
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is a multicenter, open label, Phase I/IIB study investigating the efficacy and safety of treatment with dacomitinib plus anlotinib as first-line therapy for patients with advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) 21-L858R mutations. This study comprises two parts: 1. A dose escalation Phase I study to determine the recommended phase II dose. 2. a multi-center, open label, randomized controlled, Phase IIB study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• ≥18 years of age and ≤75 years;

• Provision of a voluntarily given, personally signed and dated, written informed consent document;

• Histologically documented, unresectable, inoperable, locally advanced, recurrent or metastatic stage IIIB or IV non-small cell lung cancer (NSCLC);

• It is acceptable for subjects with the presence of EGFR activating mutation (exon 19 deletion and the L858R mutation in exon 21) to be included in this Phase I study; Only subjects with the L858R mutation in exon 21 to be included in this Phase IIb;

• At least one measurable disease by RECIST criteria version 1.1;

• Patients with controlled or stable brain metastases;

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1, and life expectancy of at least 3 months;

• No prior treatment with systemic therapy for advanced NSCLC, including TCM treatments;

• Able to comply with required protocol procedures and able to receive oral medications;

⁃ Adequate organ function, including:

‣ (1) Adequate bone marrow function Hemoglobin≥90g/L, absolute neutrophil count (ANC) should be ≥ 1.5x109/L, platelets should be ≥ 80x109/L; (2) Adequate liver function Total bilirubin ≤ 1.5 x upper normal limit (ULN), Aspartate Aminotransferase (AST) (SGOT) ≤ 2.5 x ULN (≤ 5.0 x ULN if hepatic metastases), Alanine Aminotransferase (ALT) (SGPT) ≤ 2.5 x ULN (≤ 5.0 x ULN if hepatic metastases), Creatinine≤ 1.5 x upper normal limit (ULN), or ≥ 60 mL/min; (3) Cardiac function: LVEF≥50% assessed by Doppler ultrasound;

Locations
Other Locations
China
Shanghai Chest Hospital
RECRUITING
Shanghai
Contact Information
Primary
Bo Zhang, MD
zb1063253078@163.com
15800386291
Time Frame
Start Date: 2022-10-13
Estimated Completion Date: 2027-05-01
Participants
Target number of participants: 140
Treatments
Experimental: Combined treatment group
Dacomitinib+Anlotinib: Patients will be treated with combined Dacomitinib and Anlotinib.
Active_comparator: Dacomitinib monotherapy group
Dacomitinib: Patients will be treated with Dacomitinib.
Sponsors
Leads: Shanghai Chest Hospital

This content was sourced from clinicaltrials.gov

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