SPECTA: Screening Cancer Patients for Efficient Clinical Trial Access

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age12+
SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC

About this trial

SPECTA is a quality assured platform for collecting clinicopathologically annotated biological material, imaging data, operative images, environmental assessment, questionnaires as well as patient-reported outcomes from cancer patients to support biospecimen-based translational research and clinical cancer research, including biomarker discovery to improve the understanding of tumor biology and cancer patients care.

Eligibility criteria

Qualifiers

Patients with pathologically confirmed selected tumor types (at site or centrally);

Mandatory availability of adequate human biological material (HBM);

Centrally performed confirmation of HBM adequacy in terms of quality and quantity for SPECTA downstream project requirements;

Age ≥ 12 years;

Disqualifiers

None

Trial design

Treatments tested in this trial

  • RP-1828 IMMUcan
  • RP-1759 AYA/TYA
  • RP-1843 Arcagen
  • RP-1920 BioRadon
  • 2148 MRD

Treatment groups

4,975 Participants
are divided into 5 treatment groups