Last updated: 11/03/2018 18:30:17

IMI PROTECT (Work Package 2): Calcium Channel Blockers and Cancer

GSK study ID
115736
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: IMI PROTECT (Work Package 2): Calcium Channel Blocker Treatments and Cancer Risk
Trial description: The studies described in this protocol are all performed within the framework of PROTECT (Pharmacoepidemiological Research on Outcomes of Therapeutics by a European ConsorTium) Workpackage 2 (WP2) and Workgroup 1. The primary aim of these studies is to develop, test and disseminate methodological standards for the design, conduct and analysis of Pharmacoepidemiological (PE) studies applicable to different safety issues and using different data sources. To achieve this, results from PE studies on 5 key adverse events (AEs) performed in different databases will be evaluated. Therefore, emphasis will be on the methodological aspects of the studies in this protocol and not on the clinical consequences of the association under investigation. The standards to develop will contribute to decreasing the discrepancies in results from different studies in the future and increase the usefulness and reliability of these studies for benefit-risk assessment in the EU.
Within WP2, five possible adverse event – drug pairs have been selected for analyses; one of these includes the possible role of calcium channel blockers (CCBs) in the risk of cancer. Analyses will address the hypothesis that CCBs modify the risk of cancer (all forms of cancer combined and various groups of cancers).
This hypothesis will be investigated using two sources of data: the UK General Practice Research Database (GPRD) and the Danish national databases. Investigations in the UK may also use The Health Improvement Network (THIN).
The primary objective of the study is to investigate the possible association between use of CCBs and risk of all forms of cancer combined, among adult patients (18 to 79 years of age during the study period, January 1, 1996 to December 31, 2009). The study will be conducted using three databases with different study designs (descriptive, cohort, population based cohort study and nested case-control) across different databases (GPRD, THIN, Danish databases) and to compare the results between databases, across designs to evaluate the impact of design/database/population differences on the outcome of the studied association.
Secondary objectives are to investigate the potential association between use of CCBs and risk of all forms of breast cancer in women; all forms of prostate cancer; and all forms of colon cancer using the same age groups and databases).
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

Change in incidence of primary cancer (all forms) cases, defined by Read codes in GPRD/THIN and ICD-10 codes in the Danish data

Timeframe: During Jan 1, 1996 to Dec 31, 2009 , cancer outcomes will be assessed as those occurring six months – 1 year, 1-4 years and more than 5 years following initiation of CCB therapy

Secondary outcomes:

Change in incidence of breast cancer cases in women only defined by Read codes in GPRD/THIN and ICD-10 codes in the Danish data

Timeframe: During Jan 1, 1996 to Dec 31, 2009, cancer outcomes will be assessed as those occurring six months – 1 year, 1-4 years and more than 5 years following initiation of CCB therapy

Change in incidence of prostate cancer cases only, defined by Read codes in GPRD/THIN and ICD-10 codes in the Danish data

Timeframe: During Jan 1, 1996 to Dec 31, 2009, cancer outcomes will be assessed as those occurring six months – 1 year, 1-4 years and more than 5 years following initiation of CCB therapy

Change in incidence of colon cancer cases only, defined by Read codes in GPRD/THIN and ICD-10 codes in the Danish data

Timeframe: During Jan 1, 1996 to Dec 31, 2009, cancer outcomes will be assessed as those occurring six months – 1 year, 1-4 years and more than 5 years following initiation of CCB therapy

Interventions:
  • Drug: CCB use
  • Enrollment:
    1
    Primary completion date:
    Not applicable
    Observational study model:
    Other
    Time perspective:
    Retrospective
    Clinical publications:
    Not applicable
    Medical condition
    Hypertension
    Product
    isradipine, lacidipine
    Collaborators
    Not applicable
    Study date(s)
    November 2011 to July 2014
    Type
    Observational
    Phase
    Not applicable

    Participation criteria

    Sex
    Female & Male
    Age
    18 - 79 years
    Accepts healthy volunteers
    No
    • First time users or non-users of a CCB from January 1, 1996 to December 31, 2009
    • Patients aged 18 to 79 years
    • Patients with any cancer recorded in the GPRD or the Danish database prior to cohort entry
    • Patients aged less than 18 years or more than 79 years

    Trial location(s)

    This study does not involve prospective enrollment of participants.

    Study documents

    No study documents available.

    Results overview

    No study documents available

    Recruitment status
    Study complete
    Actual primary completion date
    Not applicable
    Actual study completion date
    2014-30-07

    Plain language summaries

    Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

    Additional information about the trial

    Not applicable
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