Long-term Clinical Study of CN128 in Thalassemia With Sever Liver Iron Overloaded Patients

NCT05355766 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2025-03-14

No results posted yet for this study

Summary

The safety and efficacy of CN128 is studied in thalassaemia with sever liver iron overloaded patients.

Conditions

Interventions

DRUG

CN128 Tablets

Iron chelator, oral tablets

Sponsors & Collaborators

  • Hangzhou Zede Pharma-Tech Co., Ltd.

    lead OTHER

Principal Investigators

  • Jianmin Luo, PhD · First Affiliated Hospital of Guangxi Medical University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-13
Primary Completion
2024-09-23
Completion
2025-03-06

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05355766 on ClinicalTrials.gov