UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000015376 |
|---|---|
| Receipt number | R000017897 |
| Scientific Title | Phase II study of modified FOLFIRINOX as first-line for advanced pancreatic cancer |
| Date of disclosure of the study information | 2014/10/08 |
| Last modified on | 2022/12/19 11:40:52 |
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Basic information
Public title
Phase II study of modified FOLFIRINOX as first-line for advanced pancreatic cancer
Acronym
modified FOLFIRINOX Study
Scientific Title
Phase II study of modified FOLFIRINOX as first-line for advanced pancreatic cancer
Scientific Title:Acronym
modified FOLFIRINOX Study
Region
| Japan |
Condition
Condition
advanced pancreatic cancer
Classification by specialty
| Hepato-biliary-pancreatic medicine |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the efficacy and safety of modified FOLFIRINOX in inoperable pancreatic cancer patients.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Phase II
Assessment
Primary outcomes
Response rate
Key secondary outcomes
Overall survival
Progression free survival
The frequency of occurrence of complication
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
modified FOLFIRINOX
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
| 75 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Histological or cytologically proved pancreatic cancer adenocarcinoma or adenosquamous carcinoma
Inoperative cases of advanced pancreatic cancer
Without other chemotherapy or radiotherapy
Age 20-75 years
ECOG Performance Status (PS) 0-1
Meets the following criteria within 14 days before enrollment
absolute neutrophil count <2000/microl, platelet count <100,00/microl, hemoglobin <9g/dl, bilirubin >2.0mg/dl, AST and ALT >150U/l, Creatinine >1.2mg/dl, Creatinine clearance test <50ml/min
Hemotype of UGT1A1 genotype is not including *6/*6, *28/*28, and *6/*28
Without anorexia
Normal ECG
An agreement is provided
Key exclusion criteria
Pulmonary fibrosis or interstitial pneumonia
Watery stool
Infection
Uncontrolled diabetes mellitus
Any serious complication
Use of Atazanavir, Flucytosine, Phenytoin, and Warfarin potassium
Pregnancy
Target sample size
28
Research contact person
Name of lead principal investigator
| 1st name | Takuji |
| Middle name | |
| Last name | Iwashita |
Organization
Gifu University Hospital
Division name
First Department of internal Medicine
Zip code
501-1193
Address
1-1 Yanagido, Gifu city, Gifu
TEL
058-230-6308
takuji@w7.dion.ne.jp
Public contact
Name of contact person
| 1st name | Mitsuru |
| Middle name | |
| Last name | Okuno |
Organization
Gifu University Hospital
Division name
First Department of internal Medicine
Zip code
501-1193
Address
1-1 Yanagido, Gifu city, Gifu
TEL
058-230-6308
Homepage URL
mkobdkl@yahoo.co.jp
Sponsor or person
Institute
Gifu University Hospital
Institute
Department
Personal name
Funding Source
Organization
Gifu University Hospital
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
Gifu University Hospital
Address
1-1 Yanagido, Gifu city, Gifu
Tel
058-230-6308
mkobdkl@yahoo.co.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
岐阜大学病院（岐阜県）
Other administrative information
Date of disclosure of the study information
| 2014 | Year | 10 | Month | 08 | 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
Completed
Date of protocol fixation
| 2014 | Year | 10 | Month | 01 | Day |
Date of IRB
| 2014 | Year | 10 | Month | 01 | Day |
Anticipated trial start date
| 2014 | Year | 10 | Month | 01 | Day |
Last follow-up date
| 2017 | Year | 09 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2014 | Year | 10 | Month | 08 | Day |
Last modified on
| 2022 | Year | 12 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000017897
