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Influence of dosing interval on immune-related adverse events and infusion reaction of nivolumab and pembrolizumab

Not Applicable
Recruiting
Conditions
eoplasms
Neoplasms
D009369
Registration Number
JPRN-jRCT1030230268
Lead Sponsor
none none
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
400
Inclusion Criteria

Patients treated with nivolumab monotherapy or pembrolizumab monotherapy at Kitasato University Hospital from April 1, 2019, to March 31, 2023

Exclusion Criteria

(i) Patients who switched from the old regimen to the new regimen
(ii) Patients who could not continue more than 2 courses of the old regimen when only the old regimen was administered
(iii) Patients with missing data in the survey items

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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