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NCT Number: NCT07046728

Efficay and Safety of DAROMUN on Patient Treated by Intralesionnal Injection: DAROMEL

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient over 18 years old with locally advanced melanoma stage IIIB, IIIC, or IIID.
  • Patient diagnosed with cutaneous melanoma or melanoma of unknown primary origin.
  • Disease progression after treatment with immunotherapy in the adjuvant or metastatic setting.
  • Patient having a contraindication to immunotherapy.
  • Patient having received at least one intralesional infusion of Daromun.

Exclusion criteria

  • Patient with uveal or mucosal melanoma.
  • Opposition to data use (withdrawal of non-opposition).

Treatment and study plan

Efficay and Safety of DAROMUN on patient treated by intralesionnal injection: DAROMEL

Other

Observationnal study with clincal data collection to evaluate the efficiency and the tolerability of DAROMUN

Primary outcomes

  1. 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)

    Objective response rate according to RECIST 1 ( Evaluation Criteria In Solid Tumors )

Secondary outcomes

  1. Pathological complete response rate (macroscopic)

    Time frame: From baseline to 13 months ( september 1, 2024 to october 31, 2025)

    Disappearance of the disease at the macroscopic levels

  2. Pathological complete response rate (microscopic)

    Time frame: From baseline to 13 months ( september 1, 2024 to october 31, 2025)

    Disappearance of the disease at the microscopic levels

Study contacts

Contact information is provided by the study sponsor or research team.

Alexandra PICARD-GAUCI

CONTACT

[email protected]

04 92 03 67 31 ext. +33

Emmanuelle Pradelli

CONTACT

[email protected]

04 92 03 66 67 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nice

Other

Registry information

Official study title

Observationnal Multicentric Study to Evaluate the Safety and the Efficacy of DAROMUN of Melanoma Patient (Resectable Stage IIIB to IIID) Treated by Intralesionnal Injection

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Jul 1, 2025
Registry last updated
Jul 1, 2025

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.