Actively Recruiting

Age: 16Years - 100Years
All Genders
Healthy Volunteers
ID05650125

PINCER Platform Study for Solid Organ Cancers to Support High Quality Translational Research

Led by University of Liverpool · Updated on 2025-08-01

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Liverpool

Lead Sponsor

C

Countess of Chester NHS Foundation Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a platform study to collect biosamples and related data from patients with solid organ cancers. The study aims to provide an efficient and high-quality source of tumor and blood samples for specific research projects, allowing better understanding of cancer biology. It includes access to both historical tumor tissue and prospective fresh tissue samples, along with matched clinical and radiological data, to create rich datasets for translational research. Participants undergoing biopsy or surgical resection as part of their routine care may provide extra tumor tissue and blood samples. Tissue is collected either during biopsy or surgery with care to ensure pathological assessment is not compromised. Historical tumor tissue blocks may also be accessed and sampled. Blood samples can be taken up to 12 months after treatment. Samples are transported to approved facilities under material transfer agreements and used only for approved sub-studies within the platform. Participants may be asked to complete quality of life questionnaires up to 12 months after treatment. Clinical, pathological, and radiological data will be securely collected and pseudoanonymized for research. Analyses are performed in approved laboratories, and samples may be shared with academic or commercial partners. The study will monitor biosample procurement over four years, with ongoing data collection and participant involvement during this period.

CONDITIONS

Brief Title

A Platform Study for solId orgaN CancERs

Who Can Participate

Age: 16Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Biopsy or surgical resection as standard of care
Not Eligible

You will not qualify if you...

  • Refusal or inability to consent
  • Pediatric patients

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

Duration - Up to 4 years

Participants provide tissue and blood samples collected during routine biopsy or surgery as part of standard care, as well as archived tissue samples identified from existing clinical databases.

1 visit at time of biopsy or surgery; additional visits may occur for archived tissue retrieval

Post-treatment Monitoring

Duration - Up to 12 months

Participants may provide blood samples and complete quality of life questionnaires up to 12 months following treatment.

Periodic visits for blood draws and questionnaire completion up to 12 months post-treatment

Trial Site Locations

Total: 1 location

1

University of Liverpool

Liverpool, United Kingdom, L69 3GB

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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