UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | C000000188 |
|---|---|
| Receipt number | R000000189 |
| Scientific Title | A phase I study of TS-1 and docetaxel for advanced gastric cancer |
| Date of disclosure of the study information | 2005/09/12 |
| Last modified on | 2005/09/08 11:13:01 |
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Basic information
Public title
A phase I study of TS-1 and docetaxel for advanced gastric cancer
Acronym
A phase I study of TS-1 and docetaxel for advanced gastric cancer
Scientific Title
A phase I study of TS-1 and docetaxel for advanced gastric cancer
Scientific Title:Acronym
A phase I study of TS-1 and docetaxel for advanced gastric cancer
Region
| Japan |
Condition
Condition
advanced gastric cancer
Classification by specialty
| Hematology and clinical oncology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To estimate the maximum tolerable dose and recommended dose of TS1 and docetaxel,and to determine the efficacy and safety of the combination of TS1 and carboplatin in patients with advanced gastric cance.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Decision of the recommended dose of TS1 and docetaxel
Key secondary outcomes
Determination of dose limited toxicity and response and safety of the combination of TS1 and docetaxel
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
TS1: 80 mg/body/day, orally 21days, every 5 weeks
Docetaxel: 15, 20, 25, or 30 mg/m2, day 1, 8, 15, every 5
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) Gastric cancer
2) At least one measurable lesion
3) Inoperable or relapsed gastric cancer
4) Prior 2 regimens of chemotherapy and no prior treatment of TS1 or docetaxel
5) Age > 20 years
6) Performance status (PS) of 0 to 1
7) Adequate main organ functions
WBC > 4000/mm3,< 12000/mm3
Plt > 100000/mm3
Hb > 8.0g/dl
GOT/GPT < 2.5 x normal range
Serum creatinine < 1.5mg/dl
8) Normal ECG (NCI-CTC < Grade 1)
9) Aural ingestion
10) Estimation of at least 3 months survival
11) Written informed consent
Key exclusion criteria
1) History of active other malignancy
2) Severe heart disease (uncontrolled angina pectoris,myocardial infarction,heart failure within 3 months
3) Uncontrolled diabetes and hypertension
4) Severe complication (infection, bowel obstruction,or hemorrhage etc.)
5) > G2 neuropathy
6) Massive pleural,cardiac,or abdominal effusion
7) Intestinal fresh hemorrhage
8) Symptomatic brain metastasis
9) Pregnant women or women willing child-bearing
10) History of severe drug allergic reaction
11) Limitation of use of TS1 or docetaxel
12) Inadequate condition diagnosed by primary physician
Target sample size
15
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Kenji Tamura MD |
Organization
Kinki University School of Medicine, Nara Hospital
Division name
Department of Medical Oncology
Zip code
Address
1248-1, Otoda, Ikoma, Nara, 630-0293, Japan
TEL
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name |
Organization
Kinki University School of Medicine, Nara Hospital
Division name
Department of Medical Oncology
Zip code
Address
1248-1, Otoda, Ikoma, Nara, 630-0293, Japan
TEL
Homepage URL
Sponsor or person
Institute
Department of Medical Oncology,
Kinki University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Department of Medical Oncology,
Kinki University School of Medicine
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
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
| 2005 | Year | 09 | Month | 12 | 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
Suspended
Date of protocol fixation
| 2002 | Year | 11 | Month | 11 | Day |
Date of IRB
Anticipated trial start date
| 2002 | Year | 12 | Month | 01 | Day |
Last follow-up date
| 2004 | Year | 12 | Month | 01 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2005 | Year | 09 | Month | 12 | Day |
Last modified on
| 2005 | Year | 09 | Month | 08 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000189
