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NCT06680726Recruiting

Research Collaboration for a Precision Oncology Program (POP)

Summary

The Precision Oncology Program (POP) research collaboration aims to help generate information about the individual tumour biology for patients with advanced malignancies, using innovative biotechnologies and patient profile comparison ("matching") against specific databases (Real-world data, RWD) and to inform about potential benefit, or lack of benefit, from a given treatment.

Inclusion criteria

• Signed informed consent • In the case of deceased persons: signed general consent • All patients with the diagnosis of a solid tumour including adenocarcinoma, squamous cell carcinoma, neuroendocrine carcinoma, sarcoma, etc • ECOG-performance status 0-2, if applicable • Willing and able to understand all project related procedures, including transfer of coded (i.e. pseudonymised) or anonymized clinical data to external partners (e.g. Roche), if applicable

Exclusion criteria

• Patients with the diagnosis of blood cancer.

Contacts

The trial team's contact details are shown on request.

See the official trial record
Status
Recruiting
Phase
—
Study type
Observational
Countries
Switzerland
Sponsor
Andreas Wicki(Other)
Protocol no.
POP
Conditions
Cancer
Interventions
Other

Treatments studied

  • Matching with RWD
  • Imaging Mass Cytometry

Collaborators

Hoffmann-La Roche, University of Zurich, University Hospital, Zürich

Locations · 1

  • Zurich, SwitzerlandUniversity Hospital Zürich (Universitätsspital Zürich)Recruiting at this site

In total, worldwide, the only site listed in the registry is recruiting.

Site status per the ClinicalTrials.gov registry (last update posted: November 8, 2024).

This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.

Other identifiers

  • 2022-02289 · other identifier

See also

Other versions

These results are indicative and do not replace medical advice — discuss them with your doctor.