drugset / Trial / NCT06226363

Phase I Study of LNF1901 in Advanced Malignant Tumors

NCT06226363 ↗

NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open, phase I dose-escalation and dose-expansion study to evaluate the safety, tolerability, initial antitumor efficacy, PK and immunogenic characteristics of LNF1901 in patients with advanced malignancies.

Timeline

Start
2024-02-01
Primary completion
2025-02-01
Completion
2027-02-01

Drugs

EvaluationDrugModalityDoseRoute
Subject LNF1901 Monoclonal antibody 0.003 mg/kg —
Subject LNF1901 Monoclonal antibody 0.03 mg/kg —
Subject LNF1901 Monoclonal antibody 0.1 mg/kg —
Subject LNF1901 Monoclonal antibody 0.3 mg/kg —
Subject LNF1901 Monoclonal antibody 1 mg/kg —
Subject LNF1901 Monoclonal antibody 2 mg/kg —
Subject LNF1901 Monoclonal antibody 3 mg/kg —

Indications