UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000058234
Receipt number R000066576
Scientific Title Clinical investigation of immunotherapeutic approaches for follicular lymphoma
Date of disclosure of the study information 2025/06/27
Last modified on 2025/06/20 11:36:03

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Basic information

Public title

Predictive method for assessing the efficacy of mosunetuzumab and epcoritamab

Acronym

Predictive method

Scientific Title

Clinical investigation of immunotherapeutic approaches for follicular lymphoma

Scientific Title:Acronym

Clinical investigation of immunotherapeutic approaches

Region

Japan


Condition

Condition

follicular lymphoma

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The first objective is to evaluate the predictive validity of peripheral T cell cytotoxicity in determining the therapeutic efficacy of mosunetuzumab and epcoritamab. The second objective is to assess the efficacy of tetracyclines in enhancing peripheral T cell cytotoxicity in vitro in patients undergoing mosunetuzumab or epcoritamab treatment.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The correlation between peripheral T cell cytotoxicity and the therapeutic efficacy of mosunetuzumab or epcoritamab.

Key secondary outcomes

The efficacy of tetracyclines in enhancing peripheral T cell cytotoxicity.


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

90 years-old >

Gender

Male and Female

Key inclusion criteria

Pathologically diagnosed as follicular lymphoma.
Scheduled to undergo mosunetuzumab or epcoritamab therapy.
Provided informed consent.

Key exclusion criteria

Deemed inappropriate by the attending physician.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Kota
Middle name
Last name Iwahori

Organization

Osaka International Cancer Institute

Division name

Department of Cancer Immunotherapy

Zip code

541-8567

Address

3-1-69 Otemae, Chuo-ku, Osaka 541-8567 Japan

TEL

+81-6-6945-1181

Email

kota.iwahori@oici.jp


Public contact

Name of contact person

1st name Kota
Middle name
Last name Iwahori

Organization

Osaka International Cancer Institute

Division name

Department of Cancer Immunotherapy

Zip code

541-8567

Address

3-1-69 Otemae, Chuo-ku, Osaka 541-8567 Japan

TEL

+81-6-6945-1181

Homepage URL


Email

kota.iwahori@oici.jp


Sponsor or person

Institute

Osaka International Cancer Institute

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Institutional Review Board of Osaka International Cancer Institute

Address

3-1-69 Otemae, Chuo-ku, Osaka 541-8567 Japan

Tel

+81-6-6945-1181

Email

rinri01@opho.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

2025 Year 06 Month 27 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

Preinitiation

Date of protocol fixation

2025 Year 05 Month 15 Day

Date of IRB

2025 Year 06 Month 14 Day

Anticipated trial start date

2025 Year 07 Month 01 Day

Last follow-up date

2027 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The correlation between peripheral T cell cytotoxicity and the therapeutic efficacy of mosunetuzumab or epcoritamab.
The efficacy of tetracyclines in enhancing peripheral T cell cytotoxicity.


Management information

Registered date

2025 Year 06 Month 20 Day

Last modified on

2025 Year 06 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066576