UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000004543
Receipt number R000005401
Scientific Title A Phase II Study of Carboplatin and Pemetrexed for elderly patients with Non-Small Cell (Non Squamous cell)Lung Cancer
Date of disclosure of the study information 2010/11/11
Last modified on 2018/06/14 12:50:16

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Basic information

Public title

A Phase II Study of Carboplatin and Pemetrexed for elderly patients with Non-Small Cell (Non Squamous cell)Lung Cancer

Acronym

A Phase II Study of Carboplatin and Pemetrexed for elderly patients with Non-Small Cell (Non Squamous cell)Lung Cancer

Scientific Title

A Phase II Study of Carboplatin and Pemetrexed for elderly patients with Non-Small Cell (Non Squamous cell)Lung Cancer

Scientific Title:Acronym

A Phase II Study of Carboplatin and Pemetrexed for elderly patients with Non-Small Cell (Non Squamous cell)Lung Cancer

Region

Japan


Condition

Condition

NSCLC
non-squamous

Classification by specialty

Pneumology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Safety and Efficacy

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

ORR

Key secondary outcomes



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

Carboplatin and Pemetrexed

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

70 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Histologically or cytrologically confirmed diagnosis of NSCLC with a adeno or large cell cartinoma.
Advanced NSCLC with documented Stage IIIB or Stage IV or recurrent disease.
Tumors must have measurable disease by RECIST version 1.1
70 years of age or older.
ECOG performance status 0 or 1.
No prior systemic treatment for NSCLC.
Any major surgery within 4 weeks of study enrollment.
No radiotherapy within 2 weeks of study enrollment.
No problem adequate organ function.


Key exclusion criteria

Subjects with interstitial pneumonia or pulmonary fibrosis.
Uncontrolled Active infection.
Subjects with symptomatic brain metastases.
Concurrent use of steroid therapy.
Uncontrolled pleural.
Subjects with previous malignancies.
Any other reason that,in the opinion of the investugator precludes the subject from participating in the study.

Target sample size

42


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Makoto Nishio

Organization

Cancer Institute Hospital of JFCR

Division name

Toracic Medical Oncology

Zip code


Address

3-8-31,Ariake Koutou-ku Tokyo,Japan

TEL

03-3570-0343

Email

mnishio@jfcr.or.jp


Public contact

Name of contact person

1st name
Middle name
Last name atsushi.horiike@jfcr.or.jp

Organization

Cancer Institute Hospital of JFCR

Division name

Toracic Medical Oncology

Zip code


Address

3-8-31,Ariake Koutou-ku Tokyo,Japan

TEL

03-3570-0343

Homepage URL


Email

atsushi.horiike@jfcr.or.jp


Sponsor or person

Institute

Toracic Medical Oncology,Cancer Institute Hospital of JFCR

Institute

Department

Personal name



Funding Source

Organization

Toracic Medical Oncology,Cancer Institute Hospital of JFCR

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


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

2010 Year 11 Month 11 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

Completed

Date of protocol fixation

2010 Year 11 Month 01 Day

Date of IRB


Anticipated trial start date

2010 Year 11 Month 01 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

2010 Year 11 Month 11 Day

Last modified on

2018 Year 06 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005401


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name