UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011354
Receipt number R000013306
Scientific Title Anti-IgE Therapy for Kimura's Disease
Date of disclosure of the study information 2013/08/02
Last modified on 2013/08/02 17:32:25

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Basic information

Public title

Anti-IgE Therapy for Kimura's Disease

Acronym

Anti-IgE Therapy for Kimura's Disease

Scientific Title

Anti-IgE Therapy for Kimura's Disease

Scientific Title:Acronym

Anti-IgE Therapy for Kimura's Disease

Region

Japan


Condition

Condition

Kimura's Disease

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the efficacy of anti-IgE therapy for Kimura's disease

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Changes of mass lesion

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

a fixed schedule of eight cycles of omalizumab 300 mg, administered subcutaneously at intervals of 2 weeks

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. patients aged >20 years old
2. patients who are unresponsive to standard therapies
3. Levels of serum IgE >30
4. patients agreed to prior written informed consent

Key exclusion criteria

1. patients who are hypersinsitive to omalizumab
2. pregnenat or breast feeding patients
3. patients who are considered inadequate

Target sample size

3


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshio Yoshihara

Organization

Tokyo Women's Medical University

Division name

Department of Otorhinolaryngology

Zip code


Address

8-1 Kawada-cho, Shinjuku-ku, Tokyo

TEL

03-3353-8111

Email



Public contact

Name of contact person

1st name
Middle name
Last name Eri Sakitani

Organization

Tokyo Women's Medical University

Division name

Department of Otorhinolaryngology

Zip code


Address

8-1 Kawada-cho, Shinjuku-ku, Tokyo

TEL

03-3353-8111

Homepage URL


Email



Sponsor or person

Institute

Tokyo Women's Medical University, Department of Otorhinolaryngolog

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 08 Month 02 Day


Related information

URL releasing protocol


Publication of results

Partially published


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

2012 Year 06 Month 05 Day

Date of IRB


Anticipated trial start date

2012 Year 09 Month 05 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 08 Month 02 Day

Last modified on

2013 Year 08 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013306


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name