Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04484064

Optimization of the Targeted Anticancer Therapies

Led by Centre Hospitalier Universitaire Vaudois · Updated on 2020-07-23

500

Participants Needed

1

Research Sites

813 weeks

Total Duration

On this page

Sponsors

C

Centre Hospitalier Universitaire Vaudois

Lead Sponsor

C

Center for Primary Care and Public Health (Unisante), University of Lausanne, Switzerland

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study includes an observational pharmacokinetic study and an interventional medication adherence study. The purpose of this study is 1) to describe the concentration-time profiles of targeted anticancer drugs and to characterize the concentration-effect/toxicity relationships in the target population of patients (observational study) and 2) to characterize patterns of adherence to oral targeted anticancer drugs and identify key-driver modifiable adherence factors in patients participating in an adherence program (interventional study).

CONDITIONS

Official Title

Optimization of the Targeted Anticancer Therapies

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Cancer patients to whom a targeted anticancer therapy is prescribed
Not Eligible

You will not qualify if you...

  • Patients incapable of judgment or participants under tutelage

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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3
+1

Trial Site Locations

Total: 1 location

1

CHUV

Lausanne, Canton of Vaud, Switzerland, 1011

Actively Recruiting

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Research Team

C

Chantal Csajka, PharmD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Optimization of the Targeted Anticancer Therapies | DecenTrialz