Trial · NCT04069065
Efficacy and Safety of Once-Daily Tacrolimus in Liver Transplant Recipients (SOUL)
NCT04069065, Phase 4, Unknown, Chong Kun Dang Pharmaceutical
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Efficacy and Safety of Once-Daily Tacrolimus in Liver Transplant Recipients (SOUL). Trials, record NCT04069065. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04069065
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Efficacy and Safety of Once-Daily Tacrolimus in Liver Transplant Recipients (SOUL)
- NCT number
- NCT04069065
- Status
- Unknown
- Phases
- Phase 4
- Enrollment
- 146 participants, estimated
- Lead sponsor
- Chong Kun Dang Pharmaceutical
- Conditions
- Liver Transplant
- Interventions
- Conversion to Once-daily Tacrolimus
- First posted
- 2019-08-28
- Last updated
- 2019-08-28
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of composite efficacy failure | until 24 weeks | composite efficacy failure include biopsy-confirmed acute rejection, graft loss, death, or follow-up failure |
| Secondary | Incidence of biopsy-confirmed acute rejection | until 24 weeks | episode of biopsy-confirmed acute rejection until 24weeks after conversion |
| Secondary | Pathological results of acute rejection | until 24 weeks | acute rejection using Banff 2016 Criteria and RAI(Rejection activity index) score; total 0\~9 |
| Secondary | Survival rate of transplanted organ | at 24 weeks | |
| Secondary | Survival rate of Patients | at 24 weeks | |
| Secondary | Serum-Cr, eGFR(estimated glomerular filtration rate) | at 24 weeks | eGFR using MDRD(Modification of Diet in Renal Disease) method |
| Secondary | Evaluate safety of TacroBell SR. cap. from number of participants with adverse events | until 24 weeks |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04069065
GET https://conductscience.org/api/trials/v1/NCT04069065/registered