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NCT03558373

The Adherence of Immunosuppressive Therapy Including Tacrolimus Once-daily in Italian Kidney Transplant Recipients

Completed Last updated 5 May 2022
What this trial tests

trial testing Immunosuppressive in Kidney Transplant in 158 participants. Completed in 26 February 2020.

Timeline
31 July 2018
Primary endpoint
26 February 2020
26 February 2020

Quick facts

Lead sponsorChiesi Farmaceutici S.p.A.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment158
Start date31 July 2018
Primary completion26 February 2020
Estimated completion26 February 2020
Sites12 locations across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Chiesi Farmaceutici S.p.A. — full company profile →

Who can join

18 and older, any sex, with Kidney Transplant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Non-adherence is widespread in the transplant community. Addressing issues associated with non-adherence remains a key challenge in transplantation, in part due to the difficulty in assessing its prevalence, as there is currently no 'gold standard' for use in routine clinical practice. The purpose of this study is to evaluate the non-adherence to immunosuppressive therapy, including tacrolimus once-daily, among Italian kidney transplant recipients receiving. Along with non-adherence evaluation, possible factors related to NA will be investigated (patient-related, condition/disease-related, therapy/treatment-related, etc.).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Immunosuppressive

Trials testing the same drug.

Other recruiting trials for Kidney Transplant

Currently open trials in the same condition.

Other Chiesi Farmaceutici S.p.A. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03558373.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing