UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000052855
Receipt number R000059026
Scientific Title JAPANESE PROSPECTIVE REAL WORLD REGISTRY OF CABOZANTINIB PLUS NIVOLUMABIN PATIENTS WITH PREVIOUSLY UNTREATED ADVANCED OR METASTATIC RENAL CELL CARCINOMA
Date of disclosure of the study information 2023/11/21
Last modified on 2023/11/21 10:14:07

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Basic information

Public title

JAPANESE PROSPECTIVE REAL WORLD REGISTRY OF CABOZANTINIB PLUS NIVOLUMABIN PATIENTS WITH PREVIOUSLY UNTREATED ADVANCED OR METASTATIC RENAL CELL CARCINOMA

Acronym

JACUMET-TR study

Scientific Title

JAPANESE PROSPECTIVE REAL WORLD REGISTRY OF CABOZANTINIB PLUS NIVOLUMABIN PATIENTS WITH PREVIOUSLY UNTREATED ADVANCED OR METASTATIC RENAL CELL CARCINOMA

Scientific Title:Acronym

JACUMET-TR study

Region

Japan


Condition

Condition

advanced or metastatic renal cell carcinoma

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

Search for biomarkers to predict the efficacy of cabozantinib/nivolumab combination therapy

Basic objectives2

Others

Basic objectives -Others

Genetic and immunological characterization of non-clear cell renal cell carcinoma(nccRCC)

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Biomarker Search

Key secondary outcomes



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

1) Patients who have given written consent to participate in this ancillary study
2) Patients for whom FFPE specimen was obtained prior to initiation of cabozantinib + nivolumab combination therapy
3) Institutions that have approved from the Ethics Review Committee for this study
4) Institutions that can provide patients' samples

Key exclusion criteria

Not applicable

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Hirotsugu
Middle name
Last name Uemura

Organization

Kindai University School of Medicine

Division name

Department Of Urology

Zip code

589-8511

Address

377-2, Ohno-higashi, Osakasayama City, Osaka

TEL

072-366-0221

Email

huemura@med.kindai.ac.jp


Public contact

Name of contact person

1st name Kazunori
Middle name
Last name Fujita

Organization

Kindai University School of Medicine

Division name

Department Of Urology

Zip code

589-8511

Address

377-2,Ohno-higashi,Osakasayama City, Osaka

TEL

072-366-0221

Homepage URL


Email

kfujita@med.kindai.ac.jp


Sponsor or person

Institute

Kinki University

Institute

Department

Personal name



Funding Source

Organization

Takeda Pharmaceutical Company Limited

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Committee, Faculty of Medicine, Kinki University

Address

377-2,Ohno-higashi,Osakasayama City, Osaka

Tel

072-366-0221

Email

zizen@med.kindai.ac.jp


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

2023 Year 11 Month 21 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


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

Open public recruiting

Date of protocol fixation

2023 Year 08 Month 29 Day

Date of IRB

2023 Year 10 Month 24 Day

Anticipated trial start date

2023 Year 11 Month 01 Day

Last follow-up date

2024 Year 10 Month 23 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Exploring biomarkers to predict response to cabozantinib plus nivolumab combination therapy through genetic and immunological analysis of the tumor microenvironment in non-clear cell renal cell carcinoma (nccRCC).


Management information

Registered date

2023 Year 11 Month 21 Day

Last modified on

2023 Year 11 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000059026