UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015916
Receipt number R000018523
Scientific Title Additional research on biomarkers in "Phase II study of panitumumab rechallenge in the third-line therapy in patients with KRAS wild-type metastatic colorectal cancer (JACCRO CC-09) "
Date of disclosure of the study information 2014/12/12
Last modified on 2018/03/08 08:49:49

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Basic information

Public title

Additional research on biomarkers in "Phase II study of panitumumab rechallenge in the third-line therapy in patients with KRAS wild-type metastatic colorectal cancer (JACCRO CC-09) "

Acronym

JACCRO CC-09AR

Scientific Title

Additional research on biomarkers in "Phase II study of panitumumab rechallenge in the third-line therapy in patients with KRAS wild-type metastatic colorectal cancer (JACCRO CC-09) "

Scientific Title:Acronym

JACCRO CC-09AR

Region

Japan


Condition

Condition

Colorectal Cancer

Classification by specialty

Gastroenterology Gastrointestinal surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Prospective exploratory reseach on the reported biomarkers (EGFR S492R) using the plasma in the metastatic colorectal cancer patients who are registered in JACCRO CC-09 study, and confirmed wild-type of KRAS gene by the paraffin-embedded section of tumor tissue. In addition, DNA of the rest performs the measurement in Cancer Panel.

Basic objectives2

Bio-availability

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Tumor-related gene variation analysis using plasma free DNA

Key secondary outcomes

The measurement in Cancer Panel


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Collecting blood 16mL at the time of before JACCRO CC-09 protocol treatment, 8 weeks after protocol treatment, and PD.

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 are registered in JACCRO CC-09 study (UMIN000011440)
(1) Approved to supply the section for this research by IRB. (2) Getting the informed consent from the patient.

Key exclusion criteria

(1) Patients who are regarded as inadequate for study enrollment by investigators (2) Patients who refuse to supply the section

Target sample size

35


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Wataru Ichikawa

Organization

Showa University Fujigaoka Hospital

Division name

Division of Medical Oncology

Zip code


Address

1-30 Fujigaoka, Aoba-ku, Yokohama, Kanagawa, 227-8501 Japan

TEL

045-971-1151

Email

wataru@med.showa-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masashi Fujii

Organization

Japan Clinical Cancer Research Organization

Division name

Office

Zip code


Address

1-14-5 Ginza, Chuo-ku, Tokyo 104-0061, Japan

TEL

03-5579-9882

Homepage URL


Email

cc09ar.dc@jaccro.or.jp


Sponsor or person

Institute

Japan Clinical Cancer Research Organization

Institute

Department

Personal name



Funding Source

Organization

Japan Clinical Cancer Research Organization

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2014 Year 12 Month 12 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

No longer recruiting

Date of protocol fixation

2014 Year 10 Month 16 Day

Date of IRB


Anticipated trial start date

2014 Year 12 Month 12 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 12 Month 11 Day

Last modified on

2018 Year 03 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018523


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name