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Life sciences · Phase 1/2 Trial
ClinicalTrials.gov · September 21, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1/2 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 (NCT06114511). This is a study registration, not published results. Lead sponsor: Sichuan Baili Pharmaceutical Co., Ltd.. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: PHASE1, PHASE2. Study type: INTERVENTIONAL. Enrollment: 78 participants (ACTUAL). Conditions: Non-small Cell Lung Cancer. Interventions: DRUG: BL-M07D1. Primary outcome measures: Phase Ib: Recommended Phase II Dose (RP2D) , Up to 21 days after the first dose; Phase II: Objective Response Rate (ORR) , Up to approximately 24 months. Brief summary: This phase Ib/II study is designed to evaluate the safety, tolerability, pharmacokinetics, and efficacy of injectable BL-M07D1 in patients with HER2-mutated, locally advanced or metastatic non-small cell lung cancer.