UMIN-CTR History

Name:  UMIN ID:


Unique ID issued by UMIN UMIN000033369
Receipt number R000038025
Scientific Title Phase I / IIa clinical trial for patients with hepatitis C or B virus derived liver cirrhosis by CBP / beta catenin inhibitor PRI-724
Date of disclosure of the study information 2018/07/18
Last modified on 2022/08/04 14:23:25

No. Disposal Last modified on Item of update
1 Insert 2018/07/12 09:29:09
2 Update 2018/07/31 11:04:13 Recruitment status
3 Update 2019/01/10 12:51:08 Co-sponsor
4 Update 2019/01/10 12:53:30 Key inclusion criteria
Key inclusion criteria
5 Update 2020/10/27 10:07:04 1st name of lead principal investigator
Last name of lead principal investigator
1st name of lead principal investigator
Last name of lead principal investigator
Zip code

Last name of contact person

Last name of contact person
Zip code
Co-sponsor
Co-sponsor
Organization
Organization
Address
Address
Tel
Email
Secondary IDs
Study ID_1
Org. issuing International ID_1
Org. issuing International ID_1
IND to MHLW
Institutions
6 Update 2020/10/27 14:51:51 Organization
7 Update 2021/04/05 14:12:34 Recruitment status
Date of IRB
Last follow-up date
8 Update 2021/04/05 14:14:22 Number of participants that the trial has enrolled
9 Update 2021/04/05 14:18:18 Organization
Organization
10 Update 2022/07/04 17:40:28 Email
Email
Email1
Email
11 Update 2022/07/04 17:45:37 Recruitment status
Date trial data considered complete
Date analysis concluded
12 Update 2022/07/04 17:47:12 Publication of results
URL related to results and publications
13 Update 2022/07/08 14:59:45 URL releasing protocol
14 Update 2022/07/28 17:58:59 URL related to results and publications
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
15 Update 2022/08/01 15:17:41 Results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
16 Update 2022/08/04 14:23:25 Results
Baseline Characteristics
Baseline Characteristics
Participant flow
Participant flow
Adverse events
Outcome measures