A Phase IB /II, Multicenter, Open-Label Study of Safety, Tolerability and Efficacy of SHR-A2102 for Injection With Adebrelimab With or Without Other Antitumor Therapy in Advanced or Metastatic Non-small Cell Lung Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The study is being conducted to evaluate the safety, tolerability and efficacy of SHR-A2102 with Adebrelimab with or without other Antitumor Therapy in Advanced or Metastatic Non-small cell lung Cancer. To explore the reasonable dosage of SHR-A2102 for Advanced or Metastatic Non-small cell lung Cancer

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
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• Have the ability to give informed consent, have signed informed and able to comply with the treatment plan to visit the tests and other procedural requirements;

• The age of signing the informed consent is 18 -70 years, regardless of gender;

• Provide archived or fresh tumor tissue for vendor test;

• At least one measurable lesion according to RECIST v1.1 criteria;

• Subjects with pathology confirmed locally advanced unresectable or metastatic non-small cell lung squamous cell carcinoma;

• The ECOG score is 0 or 1;

• Expected survival ≥12 weeks

• Good level of organ function

• Male subjects whose partners are women of childbearing age and female subjects who are fertile are required to use highly effective contraceptive methods.

Locations
Other Locations
China
Chinese People's Liberation Army General Hospital
RECRUITING
Beijing
Contact Information
Primary
Yanhua Huang
yanhua.huang@hengrui.com
0518-82342973
Time Frame
Start Date: 2024-07-30
Estimated Completion Date: 2026-10
Participants
Target number of participants: 248
Treatments
Experimental: Treatment group A
SHR-A2102+Adebrelimab+Cisplatin/ Carboplatin
Sponsors
Leads: Shanghai Hengrui Pharmaceutical Co., Ltd.

This content was sourced from clinicaltrials.gov

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