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A Phase II, Multicentre, Parallel Group, Open Label, Randomised Clinical Trial of Neoadjuvant Nivolumab and Ipilimumab Combined With Relatlimab for Patients With Resectable Advanced Melanoma Identified as Poor Responders to Immunotherapy

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This clinical trial is for patients with stage 3 cutaneous melanoma and patients with mucosal melanoma who are able to have surgery to remove all tumour deposits. To improve the chance that melanoma will not recurr, new experimental combinations of a type of treatment called immunotherapy will be given before surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 1\. Written informed consent

• 2\. Male or female patients who are at least 18 years of age on the day of signing informed consent.

• 3\. Clinically detectable disease, and/or RECIST version 1.1 defined disease, and/or disease confirmed on PET imaging.

• 4\. Fully resectable disease defined as having no significant vascular, central nervous system or bony involvement. Only cases where a complete surgical resection leading to tumour free margins and which is safely achieved is considered resectable.

• 5\. Concurrent primary disease and lymph node metastases acceptable provided completely resectable.

• 6\. Up to 3 in-transit metastases are permitted as long as these are fully resectable.

• 7\. Tumour that is amenable to a newly obtained core biopsy for performance of the multi-omic predictive biomarker model

• 8\. ECOG performance status of 0 to 1.

• 9\. Adequate haematological, hepatic, renal and endocrine function

• 10\. An anticipated life expectancy of \>12 months.

• 11\. Women of child bearing potential (WOCBP) must agree to avoid pregnancy or breast feeding for the duration of study treatment.

• a. Histologically confirmed diagnosis of cutaneous melanoma or unknown primary melanoma

• b. AJCC 8th Ed Stage IIIB, IIIC, IIID cutaneous melanoma

• c. No prior systemic treatment for cutaneous melanoma

• d. Completion of the multi-omic predictive biomarker model within 14 days (7-10 business days) of planned randomisation.

• a. Histologically confirmed diagnosis of cutaneous melanoma or unknown primary melanoma

• b. AJCC 8th Ed Stage IIIB, IIIC, IIID cutaneous melanoma

• c. Disease progression on neoadjuvant anti-PD-1 monotherapy, where progressed disease is completely resectable or, disease recurrence on adjuvant anti-PD-1 monotherapy, where recurrent disease is completely resectable

• d. No prior treatment with CTLA-4 or LAG-3 inhibitors.

• a. Histologically confirmed diagnosis of mucosal melanoma

• b. Any stage of disease provided it is fully resectable

• c. No prior systemic treatment for mucosal melanoma

Locations
Other Locations
Australia
Melanoma Institute Australia
RECRUITING
Wollstonecraft
Contact Information
Primary
Monica Osorio
Monica.Osorio@melanoma.org.au
+612 9911 7296
Time Frame
Start Date: 2026-02-09
Estimated Completion Date: 2038-01
Participants
Target number of participants: 494
Treatments
Experimental: Treatment Arm A
Ipilimumab at 3 mg per kg with nivolumab at 1 mg per kg will be administered on days 1 and 22 (Q3W) in the neoadjuvant period for a total of 2 doses.
Experimental: Treatment Arm B
Ipilimumab 1mg per kg and the fixed dose combination nivolumab 480 mg and relatlimab 160 mg will be administered on days 1 and 29 (Q4W) for a total of 2 doses.
Experimental: Treatment Arm C
Fixed dose combination of nivolumab 480 mg and relatlimab 160 mg alone, to be administered on days 1 and 29 (Q4W) for a total of 2 doses.
Active_comparator: Treatment Arm D (Cohort 1a)
Ipilimumab at 1 mg per kg with nivolumab at 3 mg per kg will be administered on days 1 and 22 (Q3W) in the neoadjuvant period for a total of 2 doses.
Active_comparator: Treatment Arm E (Cohort 1b)
Ipilimumab at 1 mg per kg with nivolumab at 3 mg per kg will be administered on days 1 and 22 (Q3W) in the neoadjuvant period for a total of 2 doses.
Active_comparator: Treatment Arm F
Pembrolizumab 200 mg will be administered on days 1 and 22 (Q3W) in the neoadjuvant period for a total of 2 doses
Related Therapeutic Areas
Sponsors
Collaborators: Bristol-Myers Squibb
Leads: Melanoma Institute Australia

This content was sourced from clinicaltrials.gov