UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005859
Receipt number R000006925
Scientific Title Immunotherapy Using HLA-A24-restricted Survivin-derived Peptide Combined with IFA and IFN-alpha for Patients with Urothelial Cancer (Phase I clinical study)
Date of disclosure of the study information 2011/06/28
Last modified on 2014/03/03 08:40:15

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Basic information

Public title

Immunotherapy Using HLA-A24-restricted Survivin-derived Peptide Combined with IFA and IFN-alpha for Patients with Urothelial Cancer (Phase I clinical study)

Acronym

Phase I clinical study of Survivin-2B peptide vaccination combined with IFA and IFN -alpha for urothelial cancer

Scientific Title

Immunotherapy Using HLA-A24-restricted Survivin-derived Peptide Combined with IFA and IFN-alpha for Patients with Urothelial Cancer (Phase I clinical study)

Scientific Title:Acronym

Phase I clinical study of Survivin-2B peptide vaccination combined with IFA and IFN -alpha for urothelial cancer

Region

Japan


Condition

Condition

Advanced or recurrent urothelial cancer

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of safety and investigation of anti-tumor effect of survivin-2B peptide combined with IFA and IFN-alpha against patients with urothelial cancer

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2

Pragmatic

Developmental phase

Phase I


Assessment

Primary outcomes

Evaluation of adverse effect

Key secondary outcomes

Evaluation of immunological and clinical responses. Immunological responses are investigated by DTH, tetramer staining, and ELISPOT assay. Clinical responses are evaluated by RECIST criteria.


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 Vaccine

Interventions/Control_1

Survivin-2B peptide vaccination at a dose of 1.0mg once and IFN-alpha at a dose of 300 million-unit twice every 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

85 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients enrolled in this study were required to conform to the following criteria: (1) to have histologically confirmed urothelial cancer, (2) to be HLA-A*2402 positive, (3) to be survivin- and HLA class I-positive in the carcinomatous lesions by immunohistochemistry, (4) to be between 20 and 85 years old, (5) to have received of surgical excision of the primary tumor and (6) to have Eastern Cooperative Oncology Group (ECOG) performance status between 0 and 3.

Key exclusion criteria

Exclusion criteria included (1) prior cancer therapy such as chemotherapy, radiation therapy, steroid therapy, or other immunotherapy within the previous 4 weeks, (2) the presence of other cancers that might influence the prognosis, (3) immunodeficiency or a history of splenectomy, (4) severe cardiac insufficiency, acute infection, or hematopoietic failure and (5) unsuitability for the trial based on clinical judgment.

Target sample size

15


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroshi Kitamura

Organization

Sapporo Medical University

Division name

Department of Urology

Zip code


Address

South-1, West-16, Chuo-ku, Sapporo, Japan

TEL

011-611-2111

Email

hkitamu@sapmed.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Toshiaki Tanaka

Organization

Sapporo Medical University

Division name

Department of Urology

Zip code


Address

South-1, West-16, Chuo-ku, Sapporo, Japan

TEL

011-611-2111

Homepage URL


Email

zappa@pop12.odn.ne.jp


Sponsor or person

Institute

Department of Urology, Sapporo Medical University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Japan Science and Technology Corporation Innovation Plaza Hokkaido, Sapporo, Japan

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Department of Pathology, Sapporo Medical University School of Medicine

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

2011 Year 06 Month 28 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications

http://dx.doi.org/10.1155/2013/262967

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

2009 Year 06 Month 30 Day

Date of IRB


Anticipated trial start date

2009 Year 07 Month 01 Day

Last follow-up date

2014 Year 02 Month 28 Day

Date of closure to data entry

2014 Year 02 Month 28 Day

Date trial data considered complete

2014 Year 02 Month 28 Day

Date analysis concluded

2014 Year 02 Month 28 Day


Other

Other related information



Management information

Registered date

2011 Year 06 Month 28 Day

Last modified on

2014 Year 03 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006925


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name