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A Study to Assess the Efficacy of WSD0922-FU in Patients With C797S+ Advanced Non-small Cell Lung Cancer

RECRUITINGPhase 2Sponsored by Wayshine Biopharm, Inc.
Actively Recruiting
PhasePhase 2
SponsorWayshine Biopharm, Inc.
Started2025-08-18
Est. completion2027-09-30
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations8 sites

Summary

This is a Phase II, Open Label, Multicenter, Single Arm Study of WSD0922-FU for Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer whose Disease has Progressed with First-Line Osimertinib Treatment and whose Tumors harbor a C797S mutation within the Epidermal Growth Factor Receptor Gene.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion criteria:

* Provision of signed and dated, written informed consent prior to any study-specific procedures, sampling and analyses.
* Male or female aged ≥18 years old.
* Histological or cytological confirmation diagnosis of NSCLC.
* Locally advanced or metastatic NSCLC, not amenable to curative surgery or radiotherapy.
* Evidence of radiological disease progression while on a previous continuous treatment with first-line Osimertinib treatment.
* Documented EGFR mutation .
* Eastern Cooperative Oncology Group (ECOG) 0-1 and a minimum life expectancy of 12 weeks.
* At least one lesion, not previously irradiated and not chosen for biopsy during the study.
* Females should have evidence of non-childbearing potential.

Exclusion criteria:

* Any investigational agents or other anticancer drugs from a previous treatment regimen or clinical study within 14 days of the first dose of study treatment.
* Any unresolved toxicities from prior therapy greater than CTCAE Grade 1.
* Symptomatic brain complications that require urgent neurosurgical or medical intervention.
* Any evidence of severe or uncontrolled systemic diseases.
* Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection.
* Past medical history of ILD.
* Inadequate bone marrow reserve or organ function as demonstrated.
* Males and females of reproductive potential.
* Known intracranial hemorrhage which is unrelated to tumor.
* Seizures requiring a change in anti-epileptic medications.

Conditions3

CancerLung CancerNon Small Cell Lung Cancer

Locations8 sites

FOMAT Oncology
Oxnard, California, 93030
Principal Investigator805-483-1185nkhan@fomatmedical.com
Cleveland Clinic Weston Hospital
Weston, Florida, 33331
Principal Investigator866-293-7866saravid@ccf.org
Karmanos Cancer Institute
Detroit, Michigan, 48201
Principal Investigator231-487-3390upretyd@karmanos.org
Hackensack Meridian Health-Southern Ocean Medical Center
Manahawkin, New Jersey, 08050
Principal Investigator609-597-6011Jatin.desani@hmhn.org
Cleveland Clinic
Cleveland, Ohio, 44195
Principal Investigator866-320-4573ADJEIA2@ccf.org

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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