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NCT06599957Recruiting

Innovative Drug Delivery Nanophotonic Platform for Implementation of Sarcoma Therapy

Source: ClinicalTrials.gov · Last updated 22 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

DEEPLY aims to improve sarcoma therapy by the development of an innovative nanophotonic delivery approach to be applied in the future as an integrated local therapy for patients with inoperable tumors or with oligometastases. The major aim of the project is the development of innovative nanocarriers loaded with chemotherapeutic agents, whose delivery will be improved by the use of an optic fiber (optoporation). After the synthesis, and characterization of NPs, a prototype will be produced and preclinically validated on patient-derived biological material. This wide comprehensive methodological approach will ensure the obtainment of robust data to be faster exploited toward clinical applications.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
10 Sept 2024
Start date
30 Aug 2024
Primary completion date
30 Aug 2026
Lead sponsor
Istituto Ortopedico Rizzoli
NCT number
NCT06599957

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 30 Aug 2024 to the primary completion date, 30 Aug 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients not affected by STSs or BSs will be excluded from the study, as well as patients with multiple primary tumors.

Who the study is looking for

  • Patients eligible for the study will be male or female, with an age ranging from 0- to 85 years, undergoing surgery or biopsy for STSs or BSs including osteosarcomas.
  • Included patients may have undergone or may be still in treatment with chemotherapy (also neo-adjuvant settings), targeted therapy, radiotherapy, or combination therapy.
  • IRST will enroll only adult patients (age \> 18 years).
  • Signed informed consent from all subjects enrolled in the study. IOR patients will have to sign both the specific project Informed Consent and the IOR Biobank Informed consent.

Age in the registry: 2 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Istituto Ortopedico Rizzoli-OSOTT
Coordinator of this site? Confirm its status
BolognaItalyRecruiting
IRCCS - Istituto Romagnolo per lo Studio Dei Tumori, Dino Amadori
Coordinator of this site? Confirm its status
MeldolaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.