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Completed Phase 4 Interventional Results available

Advancing Renal TRANSplant eFficacy and Safety Outcomes With an eveRolimus-based regiMen (TRANSFORM)

ClinicalTrials.gov ID: NCT01950819

Public ClinicalTrials.gov record NCT01950819. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 3:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 24 Month, Multicenter, Randomized, Open-label Safety and Efficacy Study of Concentration-controlled Everolimus With Reduced Calcineurin Inhibitor vs Mycophenolate With Standard Calcineurin Inhibitor in de Novo Renal Transplantation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a 2-year, randomized, multicenter, open-label, 2-arm study evaluating the graft function of everolimus and reduced CNI versus MPA and standard CNI in adult de novo renal transplant recipients.

Study identification

NCT ID
NCT01950819
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
2,037 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 3, 2013 (Actual)
Primary completion
Feb 1, 2017 (Actual)
Completion
Jan 17, 2018 (Actual)
Last update posted
Jan 30, 2019

2013 – 2018

United States locations

U.S. sites
40
U.S. states
21
U.S. cities
35
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35233 —
Novartis Investigative Site Loma Linda California 92354 —
Novartis Investigative Site Los Angeles California 90033 —
Novartis Investigative Site Los Angeles California 90048 —
Novartis Investigative Site Sacramento California 95817-1460 —
Novartis Investigative Site San Diego California 92123 —
Novartis Investigative Site San Francisco California 94115 —
Novartis Investigative Site San Francisco California 94143-0116 —
Novartis Investigative Site Aurora Colorado 80045 —
Novartis Investigative Site Denver Colorado 80210 —
Novartis Investigative Site Chicago Illinois 60612 —
Novartis Investigative Site Baltimore Maryland 21201 —
Novartis Investigative Site Boston Massachusetts 02114 —
Novartis Investigative Site Boston Massachusetts 02215 —
Novartis Investigative Site Burlington Massachusetts 01805 —
Novartis Investigative Site Ann Arbor Michigan 48109-0331 —
Novartis Investigative Site Detroit Michigan 48202 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Livingston New Jersey 07039 —
Novartis Investigative Site Buffalo New York 14215 —
Novartis Investigative Site The Bronx New York 10467 —
Novartis Investigative Site Chapel Hill North Carolina 27599 —
Novartis Investigative Site Durham North Carolina 27710 —
Novartis Investigative Site Winston-Salem North Carolina 27157 —
Novartis Investigative Site Cleveland Ohio 44106-5048 —
Novartis Investigative Site Cleveland Ohio 44195 —
Novartis Investigative Site Columbus Ohio 43210 —
Novartis Investigative Site Harrisburg Pennsylvania 17105-8700 —
Novartis Investigative Site Providence Rhode Island 02903 —
Novartis Investigative Site Charleston South Carolina 29425 —
Novartis Investigative Site Nashville Tennessee 37212-3139 —
Novartis Investigative Site Dallas Texas 75246 —
Novartis Investigative Site Fort Worth Texas 76104 —
Novartis Investigative Site Houston Texas 77030-2400 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Salt Lake City Utah 84132 —
Novartis Investigative Site Charlottesville Virginia 22908 —
Novartis Investigative Site Seattle Washington 98195 —
Novartis Investigative Site Madison Wisconsin 53705 —
Novartis Investigative Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 144 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01950819, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 30, 2019 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01950819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →