UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047107
Receipt number R000053720
Scientific Title observational study to investigate the safety and efficacy of olaparib combined with bevacizumab therapy after primary chemotherapy plus bevacizumab for Japanese patients with advanced ovarian, fallopian tube, or primary peritoneal cancer.
Date of disclosure of the study information 2022/03/07
Last modified on 2023/09/07 09:52:46

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Basic information

Public title

A observational study to investigate the safety and efficacy of olaparib combined with bevacizumab therapy after primary chemotherapy plus bevacizumab for Japanese patients with advanced ovarian, fallopian tube, or primary peritoneal cancer.

Acronym

JGOG3030

Scientific Title

observational study to investigate the safety and efficacy of olaparib combined with bevacizumab therapy after primary chemotherapy plus bevacizumab for Japanese patients with advanced ovarian, fallopian tube, or primary peritoneal cancer.

Scientific Title:Acronym

JGOG3030

Region

Japan


Condition

Condition

Ovarian cancer, Fallopian tube cancer, Primary peritoneal cancer

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

To confirm the safety, efficacy, and treatment details of Olaparib plus Bevacizumab as maintenance therapy in the initial treatment of advanced ovarian cancer (including fallopian tube cancer or primary peritoneal cancer) in Japan.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Incidence of adverse events

Key secondary outcomes

-Progression-free survival (PFS) and PFS rate
-Response rate in patients with residual disease (ORR)
-Overall survival (OS)
-Relationship to subsequent therapy, platinum-free interval
-Incidence of secondary cancer


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

1. Patients diagnosed with ovarian, fallopian tube, or primary peritoneal cancer
2. Patients diagnosed with FIGO(2014) stage III or IV
3 .Patients with complete or partial response by the initial platinum-based chemotherapy
4. Patients who started Olaparib plus bevacizuma maintenance therapy after January 2021
5. Japanese female patients aged =>18 years (At the time of niraparib administration)

Key exclusion criteria

1. Patients with active double cancer
2. Patients judged by the investigator to be inappropriate for participation in this study

Target sample size

300


Research contact person

Name of lead principal investigator

1st name Junzo
Middle name
Last name Hamanishi

Organization

Kyoto University Graduate School of Medicine

Division name

Department of Gynecology and Obstetrics

Zip code

606-8507

Address

54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, Japan 606-8507.

TEL

0757513269

Email

jnkhmns@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name Junzo
Middle name
Last name Hamanishi

Organization

Kyoto University Graduate School of Medicine

Division name

Department of Gynecology and Obstetrics

Zip code

606-8507

Address

54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, Japan 606-8507.

TEL

0757513269

Homepage URL

https://jgog.gr.jp/

Email

jnkhmns@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Japanese Gynecologic Oncology Group

Institute

Department

Personal name



Funding Source

Organization

Japanese Gynecologic Oncology Group

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Japanese Gynecologic Oncology Group

Address

4F, Komatsu Building, 6-22, Kagurazaka, Shinjuku-ku, Tokyo, JAPAN, 162-0825.

Tel

03-5206-1982

Email

info@jgog.gr.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

京都大学(京都府)


Other administrative information

Date of disclosure of the study information

2022 Year 03 Month 07 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

2022 Year 02 Month 15 Day

Date of IRB

2022 Year 05 Month 02 Day

Anticipated trial start date

2022 Year 08 Month 15 Day

Last follow-up date

2028 Year 05 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Patients background, adverse events and prognosis in patients with newly diagnosed advanced ovarian cancer (including fallopian tube or primary peritoneal cancer) who received Olaparib and Bevacizumab maintenance therapy after primary chemotherapy


Management information

Registered date

2022 Year 03 Month 07 Day

Last modified on

2023 Year 09 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053720