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Life sciences · Phase 1 Trial
ClinicalTrials.gov · October 14, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07105176). This is a study registration, not published results. Lead sponsor: Hangzhou Huasai Biomedicine Co., Ltd.. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 12 participants (ESTIMATED). Conditions: Advanced Non-Small Cell Lung Cancer. Interventions: DRUG: Cyclophosphamide; DRUG: Fludarabine; DRUG: IL-2 (interleukin 2). Primary outcome measures: Adverse Events (AE) , 12 months; Serious Adverse Events (SAE) , 12 months; Objective Response Rate (ORR) , Up to 36 months; Time-to-response (TTR) , Up to 36 months; Duration of Response (DOR) , Up to 36 months; Disease Control Rate (DCR) , Up to 36 months. Brief summary: An Open-Label, Single-Arm Phase Ib Clinical Trial Evaluating the Safety, Tolerability, and Preliminary Efficacy of HS-IT101 Injection in Subjects with Advanced NSCLC.