A Study to Evaluate Safety and Efficacy of WSD0922-FU Combo With Osimertinib for NSCLC

NCT ID: NCT07206498

Last Updated: 2025-11-28

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-10-17
• Study Completion Date: 2029-10-14

Brief Summary

This is a Phase I/II, Open Label Study of WSD0922-FU in Combination with Osimertinib for Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer whose disease has progressed with third-generation EGFR-TKI with C797S mutation or is newly diagnosed with CNS metastasis with EGFR Del19 or L858R mutation

Detailed Description

WSD0922-FU is a potent reversible inhibitor of both the single EGFRm+ and dual EGFRm+/C797S+ receptor forms of EGFR with selectivity margin over wild-type EGFR. This study aims to explore the safety, tolerability, pharmacokinetic characteristics and efficacy of WSD0922-FU combined with Osimertinib in patients with non-small cell lung cancer (NSCLC) with C797S mutation after first-line third-generation EGFR-TKI resistance, and then further confirm the safety and efficacy for newly diagnosed NSCLC BM patients with classical EGFR Del19 or L858R mutation

Conditions

Non Small Cell Lung Cancer (NSCLC)

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Dose escalation (WSD0922-FU and Osimertinib)

Patients receive 80mg Osimertinib PO QD and WSD0922-FU PO QD. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT, MRI, and blood sample collection on study.

Group Type: EXPERIMENTAL

Osimertinib (Tagrisso®)

Intervention Type: DRUG

Drug: Osimertinib Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: Osimertinib Given PO, 80mg, once daily

WSD0922-FU

Intervention Type: DRUG

Drug: WSD0922-FU Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: WSD0922-FU Given PO

Dose expansion (WSD0922-FU and Osimertinib)

Patients receive 80mg Osimertinib PO QD and WSD0922-FU PO QD using dosage selected from Dose escalation. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT, MRI, and blood sample collection on study.

Group Type: EXPERIMENTAL

Osimertinib (Tagrisso®)

Intervention Type: DRUG

Drug: Osimertinib Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: Osimertinib Given PO, 80mg, once daily

WSD0922-FU

Intervention Type: DRUG

Drug: WSD0922-FU Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: WSD0922-FU Given PO

Interventions

Osimertinib (Tagrisso®)

Drug: Osimertinib Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: Osimertinib Given PO, 80mg, once daily

Intervention Type: DRUG

WSD0922-FU

Drug: WSD0922-FU Procedure: Biospecimen Collection - blood samples Undergo collection of blood samples

Procedure: Computed Tomography and/or Magnetic Resonance Imaging Undergo CT and/or MRI

Drug: WSD0922-FU Given PO

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• ≥Age 18, gender is not limited;
• Locally advanced or metastatic NSCLC confirmed by pathology;
• Patients who have been genetically tested to carry EGFR sensitive mutations;
• Blood/Tissue samples must be provided for testing;
• Must have a minimum life expectancy of >= 3 months;
• At least one measurable tumor lesion according to RECIST version 1.1; ● Previous radiotherapy-treated lesions cannot be used as target lesions unless imaging studies show clear progression of the lesions.
• Physical Status (ECOG PS) score was 0-1;
• Have full organ function;
• Eligible patients (male and female) who are fertile must agree to use a reliable contraceptive method ;
• Subjects are required to give informed consent to this study before the experiment and sign a written informed consent voluntarily.

Exclusion Criteria

• Received chemotherapy, radiotherapy, biological therapy, targeted therapy, endocrine therapy, immunotherapy, or other anti-tumor drug treatments within 4 weeks before the first administration of the study drug.
• Have previously received more than two EGFR-TKI inhibitors for part A;
• Received major organ surgery (excluding puncture biopsy) or significant trauma within 4 weeks before the first administration, or require elective surgery during the trial period.
• Used strong CYP3A4 inhibitors or strong CYP3A4 inducers within 7 days before the first use of the study drugs.
• Adverse reactions from previous anti-tumor treatments have not recovered to NCI-CTCAE v5.0 grade ≤1 (except for toxicities judged by the researcher to have no safety risks, such as hair loss, grade 2 peripheral neurotoxicity, and stable thyroid function after hormone replacement therapy).
• Skin/pressure ulcers, chronic leg ulcers, known active gastric ulcers, or non-healing wounds.
• History of severe allergies, or allergies to any active or inactive ingredients of the study drug;
• Severe infections requiring intravenous antibiotic infusion or hospitalization at the time of screening; or uncontrollable active infections within 4 weeks before administration;
• Known active or suspected autoimmune diseases; or known active ocular diseases (such as active wet age-related macular degeneration, diabetic retinopathy with macular edema);
• Human immunodeficiency virus (HIV) (HIV1/2 antibody) positive, syphilis spirochete antibody positive .
• Patients with interstitial lung disease.
• History of severe cardiovascular diseases.
• Unable to orally swallow medication, or there is a condition that significantly affects gastrointestinal absorption as judged by the researcher; Clinical intervention is required for pleural effusion, ascites (excluding subjects who do not need drainage and have been stable for more than 2 weeks after drainage).
• Known alcohol or drug dependence.
• Mental disorders or poor compliance;
• Pregnant or lactating women;
• The investigator believes that the subject has other reasons that make them unsuitable for participating in this clinical study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Wayshine Biopharm, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Shanghai East Hospital

Shanghai, , China

Site Status: RECRUITING

Countries

China

Central Contacts

lily Liu, MD

Role: CONTACT

lily.liu@wayshinebiopharm.com

+8613818880308

Wei Zhong, PhD

Role: CONTACT

wei.zhong@wayshinebiopharm.com

1-951-547-4692

Facility Contacts

Fei Zhou, MD

Role: primary

fei.zhou@tongji.edu.cn

+86 21-38804518

Other Identifiers

WSD0922-103

Identifier Type: -

Identifier Source: org_study_id