Study on Efficacy and Safety of HRS-4508 in Subjects With Locally Advanced or Metastatic Non-small Cell Lung Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The study is being conducted to evaluate the efficacy, safety, and ORR of HRS-4508 in subjects with locally advanced or metastatic non-small cell lung cancer; Evaluate the pharmacokinetic (PK) characteristics of HRS-4508 and other efficacy endpoints for the treatment of locally advanced or metastatic non-small cell lung cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Age: 18 to 80 years old; Both men and women are welcome;

• Locally advanced or metastatic non-small cell lung cancer that has failed standard treatment or cannot tolerate standard treatment regimens.

• ECOG ratings of 0 or 1.

• Expected survival period ≥ 12 weeks.

• At least one measurable lesion outside the central nervous system that meets the RECIST v1.1 standard definition.

• Willing to participate and comply with the requirements of the research protocol, and willing to cooperate with follow-up visits.

Locations
Other Locations
China
Shanghai Pulmonary Hospital
RECRUITING
Shanghai
Contact Information
Primary
Liju Zong
liju.zong@hengrui.com
0518-82342973
Time Frame
Start Date: 2025-09-12
Estimated Completion Date: 2028-07
Participants
Target number of participants: 120
Treatments
Experimental: HRS-4508 tablet
Sponsors
Leads: Jiangsu HengRui Medicine Co., Ltd.

This content was sourced from clinicaltrials.gov

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