Standardization of a Platform of Preclinical Models Derived From NSCLC Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRegina Elena Cancer Institute

About this trial

Characterize and trace innovative nutraceuticals based on microencapsulated resveratrol and Cynara cardunculus extract, using preclinical models such as organotypic tissue slices and tumoroids created from tumor fragments derived from patients with non-small cell lung cancer. This will enable the development of combination therapies to increase the efficacy of immunotherapy in NSCLC and reduce side effects that lead to treatment discontinuation.

The market implementation of these products may offer unique advantages, including increased clinical efficacy, improved tolerability of immune checkpoint inhibitors, reduced healthcare costs, improved quality of life for patients and their families, traceability of naturally derived products, and environmental sustainability.

Eligibility criteria

Qualifiers

Patients over 18 years of age;

Patients diagnosed with resectable NSCLC who will undergo curative surgery;

Patients who give written informed consent (study participation and data processing).

Disqualifiers

Previous malignancies;

Previous systemic treatments.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

5 Participants
are grouped into 1 trial group

Sponsors and collaborators

Regina Elena Cancer Institute

Lead sponsor

University of Catanzaro

Collaborator