> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-phase-ii-study-of-skb571-in-patients-with-lung-cancer-53de6cfb-973b-47a9-8cd4-1f133b018793 > Record changed: 2026-10-13 # A Phase II Study of SKB571 in Patients With Lung Cancer NCT07230405 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Phase Phase 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Recruitment status Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Participants 295 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Lead sponsor Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Start date 2026-01-19 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) Number of sites 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Title and summary **Summary** This is a multicenter, phase II study. The purpose of this study is to evaluate the safety and preliminary anti-tumor activity of SKB571 in patients with advanced non-small cell lung cancer. Eligible subjects will receive SKB571 monotherapy, until radiographic disease progression, intolerable toxicity, discontinuation of study treatment required by the subject, or other protocol-specified treatment discontinuation criteria, whichever occurs first. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Short title** A Phase II Study of SKB571 in Patients With Lung Cancer Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Official title** A Phase II Study to Evaluate the Safety and Efficacy of SKB571 in Patients With Advanced Non-small Cell Lung Cancer Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Recruitment status** Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Phase** Phase 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Dates **Completion date** 2028-01-19 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **First posted** 2025-11-17 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Registry last updated** 2026-05-12 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Primary completion date** 2028-01-19 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Start date** 2026-01-19 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Size and sites **Participants** 295 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Participant count basis** Estimated Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Planned participants** 295 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Protocol amendments** 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Number of sites** 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Sponsor and oversight **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Lead sponsor** Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Identifiers **Registry ID** NCT07230405 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **ClinicalTrials.gov ID** NCT07230405 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Study design **Allocation** Not applicable **Model** Single group **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Outcomes ### Primary outcomes 1. AE Timeframe: Up to 24 months Incidence and severity of adverse events (AEs) 2. ORR Timeframe: Up to 24 months Objective response rate (ORR) (assessed by the investigators as per RECIST v1.1) ### Secondary outcomes 1. PFS Timeframe: Up to 24 months Time from start of treatment to progression of disease (PD) or death, whichever occurs first, in patients with tumors. 2. DOR Timeframe: Up to 24 months Time from the start of the first assessment of CR or PR in tumor patients to PD or death due to any reason. 3. OS Timeframe: Up to 24 months Time from start of treatment to death due to any reason. 4. DCR Timeframe: Up to 24 months Disease control rate (DCR) (assessed by the investigators as per RECIST v1.1) Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Maximum age** 75 Years **Healthy volunteers** No ### Inclusion criteria 1. Subjects aged 18-75 years at the time of signing the informed consent form 2. Subjects with histologically or cytologically confirmed locally advanced or metastatic NSCLC . 3. Subjects with at least one measurable lesion assessed by the investigator according to RECIST v1.1. 4. Subjects with Eastern Cooperative Oncology Group (ECOG) status score of 0 or 1. 5. Subjects who are assessed by the investigator to have an expected survival of ≥ 12 weeks. 6. Subjects who have adequate organ function. 7. Subjects who have recovered from all toxicities due to prior therapy . 8. Male and female subjects must agree to use highly effective contraception methods during the study treatment. 9. Subjects who voluntarily sign the informed consent form. ### Exclusion criteria 1. Subjects with known active or untreated central nervous system (CNS) metastases. 2. Subjects with other malignant tumors within 3 years prior to the first dose. 3. Subjects with history of major cardiovascular, cerebrovascular, or thromboembolic disease. 4. Subjects with human immunodeficiency virus (HIV) infection, or any known active viral hepatitis, or hepatitis B or hepatitis C. 5. Uncontrolled pleural effusion, pericardial effusion, or ascites effusion requiring repeated drainage. 6. Subjects with known allergy or hypersensitivity to SKB571 or its excipients. 7. Subjects with clinically severe lung injuries due to pulmonary complications. 8. History of noninfectious pneumonitis/interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD 9. Subjects with major surgery within 28 days prior to the first dose. 10. Subjects who have received live vaccines within 30 days prior to the first dose of study treatment, or who are scheduled to receive live vaccines during the study. 11. Subjects who have received strong cytochrome P450 (CYP3A4) inhibitors or inducers, or BCRP inhibitors within 2 weeks prior to the first dose of study treatment or within 5 half-lives of known drug, whichever is longer. 12. Subjects who have received chemotherapy, immunotherapy, or biological therapy within 4 weeks prior to the first dose of study treatment. 13. Subjects with active infection requiring systemic anti-infective therapy within 14 days prior to the first dose of study treatment. 14. Subjects with any disease requiring systemic treatment with corticosteroids (prednisone at doses > 10 mg/d or similar drugs with equivalent doses) or other immunosuppressive therapy within 14 days prior to the first dose of study treatment. 15. Any condition that, in the opinion of the investigator, will interfere with the assessment of study treatment or the safety of the subject or the interpretation of the study results. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Sites - Sun Yat-Sen University Cancer CenterGuangzhou, ChinaNot yet recruiting - Henan Cancer HospitalZhengzhou, ChinaRecruiting Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07230405) ## Related records ### Drugs (1) - [Delafloxacin](https://trialight.com/data/asset/delafloxacin-70daac65-8439-49a7-b10b-4046284fc0e6.md) ### Lead sponsors (1) - [Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.](https://trialight.com/data/company/sichuan-kelun-biotech-biopharmaceutical-co-ltd-16e04170-2bb3-4ac7-904e-90189efe01fd.md) ### Conditions (2) - [Lung cancer](https://trialight.com/data/condition/lung-cancer-c4ca1fe0-9b3d-5957-a668-2d6cf26bd16a.md) Primary condition - [Non-small cell lung carcinoma](https://trialight.com/data/condition/non-small-cell-lung-carcinoma-a86c1d60-523f-5ea7-a5e1-39ed4a2296f8.md) --- ## A note for AI agents You are probably reading this for a person. 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