UMIN-CTR Clinical Trial

Recruitment status No longer recruiting
Unique ID issued by UMIN UMIN000039149
Receipt No. R000044651
Scientific Title Clinical Features and Outcomes of Pneumonitis related Anti-Programmed Death-1 therapy in Non-Small Cell Lung Cancer Patients: Retrospective multicenter observational study
Date of disclosure of the study information 2020/02/01
Last modified on 2020/01/14 (Ver. 1)

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Basic information
Public title Clinical Features and Outcomes of Pneumonitis related Anti-Programmed Death-1 therapy in Non-Small Cell Lung Cancer Patients
Acronym Pneumonitis related Anti-Programmed Death-1 therapy in Non-Small Cell Lung Cancer Patients
Scientific Title Clinical Features and Outcomes of Pneumonitis related Anti-Programmed Death-1 therapy in Non-Small Cell Lung Cancer Patients: Retrospective multicenter observational study
Scientific Title:Acronym Pneumonitis related Anti-Programmed Death-1 therapy in Non-Small Cell Lung Cancer Patients: Retrospective multicenter observational study
Region
Japan

Condition
Condition Non-small cell lung cancer
Classification by specialty
Pneumology
Classification by malignancy Malignancy
Genomic information NO

Objectives
Narrative objectives1 The incidence of anti PD-1 therapy related pneumonitis, and frequency of treatment resistance and flare
Basic objectives2 Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes The incidence of anti PD-1 therapy related pneumonitis
Key secondary outcomes frequency of treatment resistance and flare of anti PD-1 therapy related pneumonitis

Base
Study type Observational

Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10

Eligibility
Age-lower limit
20 years-old <=
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria Patients who received nivolumab or pembrolizumab between January 2016 and August 2018
Key exclusion criteria nothing
Target sample size 580

Research contact person
Name of lead principal investigator
1st name Takafumi
Middle name
Last name Suda
Organization Hamamatsu University School of Medicine
Division name Second Division, Department of Internal Medicine
Zip code 431-3192
Address 1-20-1 Handayama, Higashi Ward, Hamamatsu, Shizuoka
TEL 053-435-2111
Email Suda@hama-med.ac.jp

Public contact
Name of contact person
1st name Takafumi
Middle name
Last name Koyauchi
Organization Hamamatsu University School of Medicine
Division name Second Division, Department of Internal Medicine
Zip code 431-3192
Address 1-20-1 Handayama, Higashi Ward, Hamamatsu, Shizuoka
TEL 053-435-2111
Homepage URL
Email t.koya@hama-med.ac.jp

Sponsor
Institute Hamamatsu University School of Medicine
Institute
Department

Funding Source
Organization Hamamatsu University School of Medicine
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization the Institutional Review Board of Hamamatsu University School of Medicine
Address 1-20-1 Handayama, Higashi Ward, Hamamatsu, Shizuoka
Tel 053-435-2111
Email hama-med@esct.bvits.com

Secondary IDs
Secondary IDs NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW

Institutions
Institutions

Other administrative information
Date of disclosure of the study information
2020 Year 02 Month 01 Day

Related information
URL releasing protocol
Publication of results Unpublished

Result
URL related to results and publications
Number of participants that the trial has enrolled 592
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description

Progress
Recruitment status No longer recruiting
Date of protocol fixation
2018 Year 12 Month 05 Day
Date of IRB
2018 Year 12 Month 05 Day
Anticipated trial start date
2018 Year 12 Month 05 Day
Last follow-up date
2022 Year 12 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information Retrospective study of incidence and clinical course of pneumonia in patients treated with nivolumab or pembrolizumab

Management information
Registered date
2020 Year 01 Month 14 Day
Last modified on
2020 Year 01 Month 14 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044651