Skip to content

A Study of Patient Adherence and Convenience to Immunosuppressive Agents in Newly Liver Transplant

A Prospective, Multi-center, Open-labeled, Randomized Clinical Trial of Patient Adherence and Convenience to Immunosuppressive Agents in Newly Liver Transplant Recipients to Compare QD Early Conversion and BID Tacrolimus Formulation.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03216447
Enrollment
150
Registered
2017-07-13
Start date
2017-11-23
Completion date
2025-09-30
Last updated
2020-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Transplantation

Keywords

adherence, conversion, advagraf, prograf

Brief summary

A study of patient adherence and convenience to immunosuppressive agents in newly liver transplant recipients - a prospective, multi-center, open-labeled, randomized clinical trial for comparison between once-daily early conversion and twice-daily tacrolimus formulation.

Detailed description

This is prospective, multi-center, open-labeled, randomized study to investigate adherence of administration of once-daily tacrolimus formulation (Advagraf®) in newly Taiwanese (Chinese) liver transplant patients. The procedure of liver transplantation will follow the site-specific procedure. Each subject will be randomized on postoperative day 15 (POD15; defined Day 14 +/- 1)

Interventions

DRUGAdvagraf

Tacrolimus prolonged-release hard capsules (QD)

DRUGPrograf

Tacolimus capsules (q12h)

Sponsors

Astellas Pharma Taiwan, Inc.
CollaboratorINDUSTRY
Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

open labeled

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patient has been fully informed and has signed an IRB approved informed consent form within 7 days (Day 7-13) prior to POD 15 and is willing and able to follow study procedure * Patient is a primary liver transplant recipient * Patient is 20 to 70 years of age * Patient should be clearly conscious, fully understand and able to answer questionnaire

Exclusion criteria

* Patient has previously received or is receiving an organ transplant other than a liver. * Patient currently requires dialysis * Recipient or donor is known to be seropositive for human immunodeficiency virus (HIV) * Patient has received a liver transplant from a non-heart beating donor * Patient who is HCV negative has received an HCV positive (HCV RNA by PCR or HCV antibody) donor liver * Patient who is HbsAg negative has received an HbsAg positive (HBV DNA by PCR or HBV antibody) donor liver * Patient has received a liver transplant from a decrease donor \> 70 years of age * Patient has a current malignancy or a history of malignancy (within the past 5 years), except hepatocellular carcinoma within UCSF Criteria and basal or non-metastatic squamous cell carcinoma of skin that has been treated successfully. * Patient is hemodynamically unstable on POD 15

Design outcomes

Primary

MeasureTime frameDescription
Adherence of administration of Advagraf in newly Taiwanese (Chinese) liver transplant patients.Visit 1 (Day 14) to Visit 6 (Day 364) - 50 weeks observation• The adherence of enrolled 150 subjects will be assessed by the Basel assessment of adherence to immunosuppressive medications scale (BAASIS)

Countries

Taiwan

Contacts

Primary ContactWei-Chen Lee
weichen@cgmh.org.tw09753-68195

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026