Analysis of Cell Count, Viability, and Immunogenicity of Discarded Newly Diagnosed Glioblastoma Tissue or Solid Tumor Tissues
2 other identifiers
observational
141
1 country
1
Brief Summary
This study examines tumor tissues and blood samples to aid in the development of therapies for brain cancer and other solid tumors. Studying samples of blood and tissue from patients with glioblastoma or other solid tumor in the laboratory may help doctors understand brain tumors and better inform future treatments.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2021
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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 3, 2021
CompletedFirst Submitted
Initial submission to the registry
March 4, 2021
CompletedFirst Posted
Study publicly available on registry
March 30, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedFebruary 10, 2026
February 1, 2026
4.4 years
March 4, 2021
February 6, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Cell yield
This will be determined for each sample. Cell yield data is measured in 106and is assumed to be normally distributed. Summary statistics of mean, standard deviation, 95% confidence interval and range will be reported.
At study completion, up to 12 months
Percentage cell viability
Percentage cell viability will be calculated by the number of viable cells divided by the cell yield. The mean will be computed using the sum of the viable cells divided by the sum of cell yield. The range of percentage cell viability and 95% confidence interval will be provided.
At study completion, up to 12 months
Study Arms (1)
Basic Science (Biospecimen collection)
Patients undergo collection of tissue sample during surgery. Patients also undergo collection of blood sample.
Interventions
Undergo collection of tissue and blood samples
Eligibility Criteria
Patients with GBM or other solid tumor and undergoing surgery
You may qualify if:
- Provide signed and dated informed consent form
- Any individual \>= 18 years old
- Patients must have GBM or other solid tumor and undergoing surgery for diagnostic and therapeutic purposes
You may not qualify if:
- Individuals less than 18 years old
- Unable to understand and give consent
- Patients who are not surgical candidates
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, 19107, United States
Biospecimen
Tissue, blood
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 4, 2021
First Posted
March 30, 2021
Study Start
February 3, 2021
Primary Completion
June 30, 2025
Study Completion
June 30, 2025
Last Updated
February 10, 2026
Record last verified: 2026-02