Open Label, Controlled, Post Marketing, Registry Study of Ribociclib (Ribo) Treatment Adherence and Patient Reported Outcomes in Participants Using ReX Technology Platform

Description

Primary Objective: • To assess the persistence of ReX technology platform use, measured by the percentage (%) of participants who used ReX: 1) throughout the study period and 2) before the treatment discontinuation. Secondary Objective: • To evaluate the impact of the ReX technology platform on ribo treatment duration and ribo dose taking adherence as compared to control group.

Conditions

Any Solid Oral Medication

Study Overview

Study Details

Study overview

Primary Objective: • To assess the persistence of ReX technology platform use, measured by the percentage (%) of participants who used ReX: 1) throughout the study period and 2) before the treatment discontinuation. Secondary Objective: • To evaluate the impact of the ReX technology platform on ribo treatment duration and ribo dose taking adherence as compared to control group.

Study of Ribociclib (Ribo) Treatment Adherence Clinical Study Protocol

Open Label, Controlled, Post Marketing, Registry Study of Ribociclib (Ribo) Treatment Adherence and Patient Reported Outcomes in Participants Using ReX Technology Platform

Condition
Any Solid Oral Medication
Intervention / Treatment

-

Contacts and Locations

Little Rock

CARTI, Little Rock, Arkansas, United States, 72205

Minneapolis

Allina, Minneapolis, Minnesota, United States, 55407

Austin

Texas Oncology, Austin, Texas, United States, 78705

Richmond

Virginia Cancer Center, Richmond, Virginia, United States, 23229

Madison

Lumicera, Madison, Wisconsin, United States, 53717

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Dosentrx Ltd.,

    Study Record Dates

    2026-01-30