Innovative Drug Delivery Nanophotonic Platform for Implementation of Sarcoma Therapy

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 85
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Italy
Istituto Ortopedico Rizzoli-OSOTT
RECRUITING
Bologna
IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori
RECRUITING
Meldola
Contact Information
Primary
Toni Ibrahim, MD Oncologist
toni.ibrahim@ior.it
+39 0516366199
Time Frame
Start Date: 2024-08-30
Estimated Completion Date: 2026-08-30
Participants
Target number of participants: 30
Treatments
Bone and soft tissue sarcomas
Patients affected by sarcoma and undergoing surgical removal of the tumor or performing a biopsy will be enrolled. Only patients whose resection will provide sufficient tumor tissue that exceed what is necessary for pathological diagnosis characterization and banking will be enrolled.
Related Therapeutic Areas
Sponsors
Collaborators: Università Degli Studi del Sannio Dipartimento di Ingegneria Benevento, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori Meldola
Leads: Istituto Ortopedico Rizzoli

This content was sourced from clinicaltrials.gov