Name: UMIN ID:
Unique ID issued by UMIN | UMIN000017092 |
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Receipt number | R000019824 |
Scientific Title | Phase 1 dose-escalation, safety / tolerability and preliminary efficacy study of intratumoral and subcutaneous administration of GEN0101 in patients with recurrence of castration resistant prostate cancer |
Date of disclosure of the study information | 2015/04/15 |
Last modified on | 2017/10/18 18:10:38 |
No. | Disposal | Last modified on | Item of update | |
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1 | Insert | 2015/04/09 23:12:08 | ||
2 | Update | 2015/05/20 15:30:39 | Key inclusion criteria Key exclusion criteria |
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3 | Update | 2015/05/20 15:44:36 | Division name Name of person sending information Name of person sending information Address Address TEL Institute |
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4 | Update | 2015/05/20 16:09:49 | Organization Organization Category of Funding Organization Nationality of Funding Organization Nationality of Funding Organization Co-sponsor Co-sponsor Institutions |
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5 | Update | 2015/05/20 16:12:25 | Institutions |
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6 | Update | 2015/05/20 16:51:24 | Interventions/Control_1 Interventions/Control_1 |
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7 | Update | 2015/06/15 11:08:04 | Recruitment status Anticipated trial start date |
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8 | Update | 2016/10/09 18:46:29 | Name of primary person or sponsor Institute Institute Organization Organization |
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9 | Update | 2016/10/09 18:52:52 | Key inclusion criteria Key inclusion criteria Key exclusion criteria Key exclusion criteria |
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10 | Update | 2017/04/10 10:36:46 | Organization Organization Division name Division name TEL |
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11 | Update | 2017/04/18 17:31:47 | Name of person sending information Name of person sending information TEL |
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12 | Update | 2017/10/11 16:34:41 | Last follow-up date Date of closure to data entry Date trial data considered complete Date analysis concluded |
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13 | Update | 2017/10/18 18:10:38 | Recruitment status |