Trials / Recruiting
RecruitingNCT07327489
Predicting Response to Immunotherapy From Analysis of Live Tumor Biopsies
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,000 (estimated)
- Sponsor
- Elephas · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will collect tumor specimens with correlated clinical and demographic data from patients who are undergoing a biopsy or similar procedure to obtain tumor tissue as a normal course of their medical management or diagnostic work-up for suspected or confirmed cancer.
Detailed description
Elephas is researching mechanisms of cutting, sorting and imaging tumors that leave the 3D tumor microenvironment (TME), including its immune cells, intact. This allows qualitative and semi-quantitative identification and characterization of the ex vivo response to exposure of potential immunotherapy. The ex vivo response data will then be compared to the clinical real world response data to inform development efforts. This study will collect tumor specimens from patients with suspected or confirmed cancer. These specimens, along with clinical data and genomic data obtained as part of a patient's standard of care, will be used to perform this research.
Conditions
- Cancer
- Immunotherapy
- Advanced Solid Tumors Cancer
- Bladder Cancer
- TNBC, Triple Negative Breast Cancer
- Colorectal Cancer
- DMMR Colorectal Cancer
- MSI-H Colorectal Cancer
- Endometrial Cancer
- Head and Neck Cancer
- Kidney Cancer
- Liver Cancer
- NSCLC (Non-small-cell Lung Cancer)
- Skin Cancer
- Melanoma (Skin Cancer)
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Biopsy | Subjects must be clinically able, at investigator discretion, to undergo additional biopsy passes during their biopsy. Biopsy specimen(s) will be obtained during a standard of care (SOC) procedure. If a subject receives a subsequent SOC biopsy for clinical diagnosis purposes, additional sample(s) may be collected and sent to the Sponsor. |
Timeline
- Start date
- 2025-04-14
- Primary completion
- 2035-04-01
- Completion
- 2038-04-01
- First posted
- 2026-01-08
- Last updated
- 2026-01-08
Locations
8 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT07327489. Inclusion in this directory is not an endorsement.