Name: UMIN ID:
Unique ID issued by UMIN | UMIN000002182 |
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Receipt number | R000001991 |
Scientific Title | A phase II study to evaluate the effectiveness of l-LV/5-FU (mRPMI regimen) + Bevacizumab for patients with advanced/recurrent colon cancer who cannot undergo common protocol (OGSG 0802) |
Date of disclosure of the study information | 2009/07/10 |
Last modified on | 2022/09/25 17:47:32 |
No. | Disposal | Last modified on | Item of update | |
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1 | Insert | 2009/07/10 16:35:10 | ||
2 | Update | 2009/07/10 16:45:24 | Acronym Acronym |
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3 | Update | 2009/12/04 17:44:16 | Recruitment status |
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4 | Update | 2011/02/24 16:02:20 | Recruitment status Last follow-up date |
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5 | Update | 2012/06/24 23:54:46 | Public title Public title Acronym Acronym |
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6 | Update | 2012/06/24 23:57:20 | Organization Organization Division name Division name Address Address TEL Post marketing survey by drug manufacture etc., specified by Japanese law. Organization1 Address1 Tel1 Email1 |
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7 | Update | 2013/01/10 20:25:16 | Recruitment status Last follow-up date |
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8 | Update | 2022/09/25 16:58:43 | Date of IRB Anticipated trial start date Last follow-up date |
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9 | Update | 2022/09/25 17:28:25 | URL releasing protocol Publication of results URL related to results and publications Number of participants that the trial has enrolled Results Results Results date posted Date of the first journal publication of results Baseline Characteristics Baseline Characteristics Participant flow Participant flow Adverse events Adverse events Outcome measures Outcome measures |
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10 | Update | 2022/09/25 17:41:20 | Key inclusion criteria Key exclusion criteria Key exclusion criteria |
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11 | Update | 2022/09/25 17:47:32 | Interventions/Control_1 Interventions/Control_1 |