UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011713
Receipt number R000013694
Scientific Title A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy
Date of disclosure of the study information 2013/09/12
Last modified on 2013/09/11 19:56:27

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Basic information

Public title

A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Acronym

A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Scientific Title

A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Scientific Title:Acronym

A phase II study of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Region

Japan


Condition

Condition

Large cell neuroendocrine carcinoma (LCNEC)

Classification by specialty

Pneumology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate efficacy and safety of Bevacizumab plus Docetaxel for advanced large cell neuroendocrine carcinoma (LCNEC) with previously treated with platinum based chemotherapy

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Phase II


Assessment

Primary outcomes

Response rate

Key secondary outcomes

Overall survival
Safety
Progression free survival


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

A combined therapy of Bevacizumab plus Docetaxel

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) Histologically or Cytlogically confirmed large cell neuroendocrine carcinoma (LCNEC)
2) Stage IIIB/IV or postoperative recurrence
3) Previously treated platinum based chemotherapy
4) Patients aged 20 years or older
5) ECOG performance status of 0-1
6) Measureable region evaluable according to the RECIST(ver.1.1)
7) Adequate organ function
8) Patients who are considered to survive for more than 4 months
9) Written informed consent from the patient

Key exclusion criteria

Severe or uncontrollable systemic disease
2) Active infection
3) Active concomitant malignancy
4) Symptomatic brain metastasis
5) Uncontrollable pleural effusion, ascites, or pericardial effusion
6) History of GI perforation
7) Tendency to hemorrhages
8) Pregnancy, breast feeding and suspected pregnancy
9) Invasion to major vessel or cavitations of tumor
10) Uncontrollable hypertension
11) Inappropriate patients for this study judged by the physicians

Target sample size

19


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazutoshi Isobe

Organization

Toho University Omori Medical Center

Division name

Department of Respiratory Medicine

Zip code


Address

6-11-1, Omori-Nishi, Ota-ku, Tokyo, Japan

TEL

03-3762-4151

Email

kazutoshiisobe@aol.com


Public contact

Name of contact person

1st name
Middle name
Last name Kazutoshi Isobe

Organization

Toho University Omori Medical Center

Division name

Department of Respiratory Medicine

Zip code


Address

6-11-1, Omori-Nishi, Ota-ku, Tokyo, Japan

TEL

03-3762-4151

Homepage URL


Email

kazutoshiisobe@aol.com


Sponsor or person

Institute

Toho University Omori Medical Center

Institute

Department

Personal name



Funding Source

Organization

None

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

2013 Year 09 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

Open public recruiting

Date of protocol fixation

2013 Year 09 Month 05 Day

Date of IRB


Anticipated trial start date

2013 Year 09 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

2013 Year 09 Month 11 Day

Last modified on

2013 Year 09 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013694


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name