drugset / Trial / NCT06521931

A Study of PN20 for the Prevention of Chemotherapy-induced Thrombocytopenia in Lymphoma or Solid Tumor Patients

NCT06521931 ↗

Phase 1 Completed 24 enrolled Chongqing Peg-Bio Biopharm Co., Ltd.
NaSingle-groupOpen-labelPrevention

Summary

The main aim of this clinical trial is to assess the safety and tolerability of PN20 in adult patients with chemotherapy-induced thrombocytopenia (CID). The main questions it aims to answer are: * Is PN20 safe in these patients? * Could these patients potentially benefit from PN20 prevention? Participants will * Receive subcutaneous injections of PN20 according to weight on the first day of chemotherapy cycle, within 1 hour before the administration of chemotherapy drugs, * Visit the clinic on Day 1 (D1), D2, D3, D4, D5, D8, D11, D13, D15 and D21 for assessment.

Timeline

Start
2023-12-06
Primary completion
2025-01-13
Completion
2025-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject PN20 Peptide 0.2 mg/kg Subcutaneous
Subject PN20 Peptide 0.5 mg/kg Subcutaneous
Subject PN20 Peptide 0.75 mg/kg Subcutaneous

Indications