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Clinical Trial Summary

The aim of this study is to investigate the safety and efficacy of the prophylactic use of Trilaciclib in patients with non-small cell lung cancer (NSCLC) receiving platinum-based chemotherapy, so as to provide more evidence-based medical evidence for the optimal diagnosis and treatment strategy in this population.


Clinical Trial Description

This is a single-arm, exploratory clinical study. Eligible patients were treated with Trilaciclib before the first cycle of chemotherapy, and their peripheral blood samples were tested on days 3,7,14,21±1 after chemotherapy. At the same time, the incidence of FN, the use of antibiotics, the safety, the number of patients who delayed the second cycle of treatment, the number of patients who reduced the dose of chemotherapy, the number of patients who reduced the dose of chemotherapy due to neutropenia, and the number of patients who discontinued chemotherapy were observed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06328049
Study type Interventional
Source Taixing People's Hospital
Contact liu C yang, M.D.
Phone 87656001
Email liuyctx@163.com
Status Recruiting
Phase Phase 2
Start date August 10, 2023
Completion date August 10, 2025

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