Squamous Non-Small Cell Lung Cancer sqNSCLC

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Review clinical trials related to Squamous Non-Small Cell Lung Cancer sqNSCLC. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Metronomic Oral Paclitaxel Plus PD-1/ PD-L1 Inhibitor Maintenance in Advanced Lung Cancer (PULSE Study)

This study will evaluate the efficacy and safety of metronomic oral paclitaxel combined with a PD-1 or PD-L1 inhibitor as maintenance therapy in patients with advanced lung cancer whose disease has not progressed after first-line chemoimmunotherapy. The study will include two independently analyzed cohorts. Cohort A will include patients with advanced squamous non-small cell lung cancer(sqNSCLC), and Cohort B will include patients with extensive-stage small cell lung cancer(ES-SCLC). All participants will receive oral paclitaxel three times weekly together with the same immune checkpoint inhibitor used during first-line induction therapy, whenever feasible. The primary outcome is progression-free survival. Other outcomes include tumor response, overall survival, adverse events, treatment tolerability, and quality of life. Approximately 107 participants will be enrolled across multiple study centers.

Participants needed: 107
Trial details
Phase: Phase 4Age: 18-75Biological sex: AllType: InterventionalSponsor: Anhui Provincial Cancer HospitalUpdated: Aug 4, 2026Locations: 1
Eligibility criteria

1. The participant has been fully informed about the study, voluntarily agrees t... [+10]

1. Known hypersensitivity to oral paclitaxel, an immune checkpoint inhibitor, or... [+8]

Status: Not yet recruiting

Evaluate the Safety, Tolerability, and Preliminary Efficacy of EVM14 in Combination With Ivonescimab in Sq-NSCLC Patients

The purpose of this clinical trial is to evaluate the safety, tolerability, preliminary efficacy, and immunogenicity of EVM14 administered intramuscularly (IM) combination with Ivonescimab in patients with sq-NSCLC.

Participants needed: 13
Trial details
Phase: Phase 1Age: 18-99Biological sex: AllType: InterventionalSponsor: Everest Medicines (Beijing) Co., Ltd.Updated: May 29, 2026
Eligibility criteria

Pathologically confirmed locally advanced (Stage IIIB/IIIC) or metastatic (Stage... [+6]

Has disease that is suitable for local treatment administered with curative inte... [+7]

Status: Not yet recruiting

Efficacy and Safety of Sintilimab Combined with Nab-PP Plus Rh-endostatin in Locally Advanced/advanced and Recurrent Metastatic Squamous Non-small Cell Lung Cancer: a Single-arm, Multicenter Clinical Study

The goal of this single-arm, multi-center phase II clinical study is to evaluate the efficacy and safety of recombinant human endostatin (rh-Endostatin) combined with nab-paclitaxel, platinum-based chemotherapy, and PD-1 inhibitors in patients with locally advanced, advanced, or recurrent metastatic squamous non-small cell lung cancer (NSCLC). The main questions it aims to answer are: What is the progression-free survival (PFS) and objective response rate (ORR) of this combination therapy? What is the safety profile, including adverse event (AE) and serious adverse event (SAE) rates? Researchers will compare the treatment effects over time by evaluating tumor responses using RECIST 1.1 criteria and assessing quality of life using the EORTC QLQ-C30 (v3.0) and QLQ-CX24 scales. Participants will: Receive 4-6 cycles of rh-Endostatin combined with nab-paclitaxel, platinum-based chemotherapy, and PD-1 inhibitors. Continue maintenance treatment with rh-Endostatin and PD-1 inhibitors until disease progression or intolerable toxicity.

Participants needed: 32
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Jian-Guo Zhou, MD, PhDUpdated: Dec 27, 2024
Eligibility criteria

Patients must voluntarily participate in the study and provide written informed... [+6]

History of severe hypersensitivity or allergic reactions to humanized antibodies... [+14]