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Clinical Trial Summary

The purpose of this study is to collect data on how advanced and rare cancers respond to biomarker-based treatments.


Clinical Trial Description

The UNIQUE umbrella protocol is an overarching framework to study precision medicine in patients with precise molecular data, who have exhausted all established treatment options and who are not eligible for any of the ongoing trials. There is no additional visit or procedure required to participate in this study. Participants who have received/who may receive the following treatments may join the study and will be assigned to a study cohort (group): - Group 1 - Health Canada approved/marketed drug(s) used on or off-label as Standard of Care (SOC) - Group 2 - Drugs accessed from Special Access Program (SAP) - Group 3 - Non-marketed investigational agents Under the UNIQUE framework, data from participants will be evaluated. The following data will be collected: - Demographic data (for example: sex, race, month and year of birth) - Medical history - Cancer characteristics including biomarkers - Treatment history - response to treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06285500
Study type Observational [Patient Registry]
Source University Health Network, Toronto
Contact Amit Oza, Dr.
Phone 416 946 4450
Email amit.oza@uhn.ca
Status Recruiting
Phase
Start date February 1, 2024
Completion date February 1, 2029

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