A Patient-Centric Platform Trial for Precision Oncology
XCELSIOR
xCures/CancerCommons Enhanced Learning Treatment Selection and Analysis With Outcomes Research (XCELSIOR) Study: A Patient-Centric Platform Trial for Precision Oncology
1 other identifier
observational
10,000
1 country
1
Brief Summary
XCELSIOR is a non-interventional data registry. Information about treatments, treatment decisions and rationale, and patient outcomes including safety and effectiveness of anti-cancer therapy and associated supportive care will be collected for analysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 2, 2019
CompletedFirst Posted
Study publicly available on registry
January 4, 2019
CompletedStudy Start
First participant enrolled
February 7, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedFebruary 3, 2023
January 1, 2023
4.9 years
January 2, 2019
January 31, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Progression Free Survival (PFS)
5 Years
Overall Survival (OS)
5 years
Eligibility Criteria
This study will initially include up to 10,000 adult and pediatric patients with recalcitrant or advanced cancers.
You may qualify if:
- Both male and female patients with known or suspected recalcitrant or advanced cancer are eligible to enroll through the Cancer Commons Website
- Patients with any performance status, comorbidity or disease severity are eligible
- Patients or their legally-authorized representative must be willing and able to provide written, informed consent (and assent, if applicable)
You may not qualify if:
- Patients must be a resident of or receiving care within the United States or US territories.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- xCureslead
- Cancer Commonscollaborator
- Musella Foundation for Brain Tumor Research and Information, Inc.collaborator
- Pediatric Oncology Experimental Therapeutics Investigators Consortiumcollaborator
Study Sites (1)
Cancer Commons
Los Altos, California, 94022, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mark Shapiro
xCures / Cancer Commons
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 5 Years
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 2, 2019
First Posted
January 4, 2019
Study Start
February 7, 2019
Primary Completion
January 1, 2024
Study Completion
January 1, 2026
Last Updated
February 3, 2023
Record last verified: 2023-01