Chu de Nice
Nice, Alpes Maritimes, 06000, France
Location contact
Alexandra PICARD-GAUCI
CONTACT
04 92 03 67 31 ext. +33
Emmanuelle Pradelli
CONTACT
04 92 03 66 67 ext. +33
NCT Number: NCT07046728
Melanoma is a malignant tumor originating from melanocytes, with a high metastatic potential, particularly in advanced stages. The standard treatment for resectable melanomas has traditionally been surgery, often followed by adjuvant therapy to reduce the risk of recurrence. However, the emergence of neoadjuvant/perioperative therapies, administered prior to surgery, has revolutionized the management of patients with stage IIIB-C-D melanoma presenting with locoregional macroscopic metastases. Another therapeutic approach involving an intratumoral immunocytokine called DAROMUN (a fusion protein combining an antibody and a cytokine), designed to stimulate antitumor immunity within the melanoma cell microenvironment, was presented at the global oncology congress (ASCO) in June 2024. Preliminary biomarker analyses indicated that treatment with DAROMUN leads to an increase in tumor-infiltrating lymphocytes, particularly CD4+ and CD8+ cells, suggesting immune activation within the tumor microenvironment. This molecule, recently made available through a compassionate use program on the website of the French National Agency for the Safety of Medicines and Health Products (ANSM), may be particularly beneficial for patients who experience recurrence despite prior adjuvant therapy and who have locally advanced, resectable melanoma.The team therefore aim to conduct a real-world, ambispective, multicenter study under the auspices of the Cutaneous Oncology Group (GCC) of the French Society of Dermatology (SFD), focusing on the use of DAROMUN in patients with stage IIIB-IIID locally advanced melanoma.The primary endpoint will be to assess the response rate to treatment according to RECIST 1.1 criteria.Secondary endpoints will include: distant metastasis-free survival, pathological complete response rate, treatment safety profile, and overall survival.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Nice, Alpes Maritimes, 06000, France
Alexandra PICARD-GAUCI
CONTACT
04 92 03 67 31 ext. +33
Emmanuelle Pradelli
CONTACT
04 92 03 66 67 ext. +33
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Observationnal study with clincal data collection to evaluate the efficiency and the tolerability of DAROMUN
Time frame: From baseline to 13 months ( september 1, 2024 to october 31, 2025)
Objective response rate according to RECIST 1 ( Evaluation Criteria In Solid Tumors )
Time frame: From baseline to 13 months ( september 1, 2024 to october 31, 2025)
Disappearance of the disease at the macroscopic levels
Time frame: From baseline to 13 months ( september 1, 2024 to october 31, 2025)
Disappearance of the disease at the microscopic levels
Contact information is provided by the study sponsor or research team.
Alexandra PICARD-GAUCI
CONTACT
04 92 03 67 31 ext. +33
Emmanuelle Pradelli
CONTACT
04 92 03 66 67 ext. +33
Centre Hospitalier Universitaire de Nice
Other
Observationnal Multicentric Study to Evaluate the Safety and the Efficacy of DAROMUN of Melanoma Patient (Resectable Stage IIIB to IIID) Treated by Intralesionnal Injection
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.