SPECTA: Screening Cancer Patients for Efficient Clinical Trial Access

  • End date
    Mar 12, 2026
  • participants needed
  • sponsor
    European Organisation for Research and Treatment of Cancer - EORTC
Updated on 16 May 2021


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.


Patients are recruited in the platform for the research purpose of 3 downstream projects. For more information, please have a look at the "Groups and cohorts" section.

Condition All Tumor Types
Treatment Biomarker assessment, NGS, IHC, RP-1828 IMMUcan, RP-1759 AYA/TYA, RP-1843 Arcagen
Clinical Study IdentifierNCT02834884
SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC
Last Modified on16 May 2021


How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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