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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05430126
Other study ID # CSU20220619
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 19, 2022
Est. completion date August 10, 2022

Study information

Verified date June 2022
Source Central South University
Contact Miao Yan, PhD
Phone +8615708460624
Email yanmiao@csu.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Although protein kinase inhibitors (PKIs) have proved effective in treating many cancers, few patients receiving PKIs may experience rare but life-threatening hepatotoxicity such as hepatic failure. Today, there is no large-scale retrospective pharmacovigilance study focusing on protein kinase inhibitors-related hepatotoxicity. The objective was to investigate reports of hepatotoxicity related to protein kinase inhibitors using FDA Adverse Event Reporting System (FAERS).


Description:

The investigators plan to include FDA approved PKIs from PKIDB, a curated, annotated and updated database of protein kinase inhibitors (https://www.icoa.fr/pkidb/). The search terms of hepatotoxicities will be extracted from "Drug related hepatic disorders-comprehensive search (SMQ)" in MedDRA (Medical Dictionary for Regulatory Activities).


Recruitment information / eligibility

Status Recruiting
Enrollment 600000
Est. completion date August 10, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Case reported in the FAERS database of individual safety case reports at the time of the extraction, - Patients treated with at least 1 PKIs. Exclusion Criteria: - Chronology not compatible between the PKIs and hepatotoxicities

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Protein Kinase Inhibitor
This retrospective pharmacovigilance study will include protein kinase inhibitor and exclude those drugs known to cause hepatotoxicities

Locations

Country Name City State
China Central South University Changsha Hunan

Sponsors (1)

Lead Sponsor Collaborator
Central South University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hepatotoxicities cases reports related to PKIs (from FAERS database). The investigators plan to identify number of cases of hepatotoxicities (especially severe toxicities such as hepatic failure) reports related to PKIs reported in the FAERS database by using reporting odds ratios (ROR) and information component (IC), two common method in disproportionality analysis. Clinical features such as gender, age and indications will be displayed, too. From 2004 to Sep, 2021
Secondary Description of the time to onset of hepatotoxicities after PKIs exposure. The investigators plan to conduct a time to onset analysis of PKIs-related hepatotoxicities using weibull distribution From 2004 to Sep, 2021
Secondary Description of the fatality cases. Fatality cases of PKIs-related hepatotocities will be described. From 2004 to Sep, 2021
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