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Completed No phase listed Observational

Observational Study of Real World Effectiveness Data and Safety in Patients Receiving Pazopanib With Advanced or Metastatic Renal Cell Carcinoma

ClinicalTrials.gov ID: NCT01649778

Public ClinicalTrials.gov record NCT01649778. 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 Sep 4, 2026, 7:45 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

PRINCIPAL: A Prospective Observational Study of Real World Treatment Patterns and Treatment Outcomes in Patients With Advanced or Metastatic Renal Cell Carcinoma Receiving Pazopanib

Brief summary

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

This is a global, multi-centre, long-term, prospective, observational study to evaluate treatment patterns and clinical outcomes in patients with advanced or metastatic RCC treated for the first time with pazopanib. The study is designed to enroll approximately 700-1000 patients in over the course of an enrollment period of approximately 18 months.There are no protocol-mandated visits or procedures associated with the study. Each patient is expected to participate for a maximum of 30 months or until premature discontinuation (i.e., due to death, withdrawal of consent, lost to follow-up or study termination).

Study identification

NCT ID
NCT01649778
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
662 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Jul 18, 2012
Primary completion
Jul 2, 2017
Completion
Jul 2, 2017
Last update posted
Jul 14, 2020

2012 – 2017

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85016
Novartis Investigative Site Orange California 92868
Novartis Investigative Site Jacksonville Florida 32256
Novartis Investigative Site Louisville Kentucky 40207
Novartis Investigative Site Shreveport Louisiana 71101
Novartis Investigative Site Jackson Mississippi 39202
Novartis Investigative Site Lincoln Nebraska 68510
Novartis Investigative Site Henderson Nevada 89052
Novartis Investigative Site The Bronx New York 10467
Novartis Investigative Site Charleston South Carolina 29414
Novartis Investigative Site Sioux Falls South Dakota 57105
Novartis Investigative Site Austin Texas 78705
Novartis Investigative Site Dallas Texas 75246
Novartis Investigative Site Fort Worth Texas 76104
Novartis Investigative Site Houston Texas 77024

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 129 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01649778, 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 Jul 14, 2020 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01649778 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →