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OncoMatch/Clinical Trials/NCT05779423

Cryoablation+Ipilimumab+Nivolumab in Melanoma

Is NCT05779423 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Ipilimumab and Nivolumab for metastatic melanoma.

Phase 2RecruitingMassachusetts General HospitalNCT05779423Data as of Jun 2026

Treatment: Ipilimumab · NivolumabThe aim of this study is to find out whether the combination of two approved drugs, ipilimumab and nivolumab, in combination with cryoablation are safe and effective for participants who have an unresectable melanoma that is resistant, or is growing, after receiving immunotherapy with a PD-1 inhibitor. The names of the study interventions involved in this study are: * Cryoablation (an interventional radiology procedure that freezes part of a tumor) * Ipilimumab (an immunotherapy) * Nivolumab (an immunotherapy)

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Extracted eligibility criteria

Treatments studied

Immunotherapy

IpilimumabNivolumab

Cancer type

Melanoma

Tumor Agnostic

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: checkpoint inhibitor (pembrolizumab, nivolumab, nivolumab-relatimab, atezolizumab, ipilimumab)

progressed on immune checkpoint inhibitor therapy (pembrolizumab, nivolumab, nivolumab-relatimab, atezolizumab, ipilimumab)

Cannot have received: combination checkpoint inhibitor (ipilimumab, nivolumab)

Exception: if combination was the last line of therapy and patient is progressing

Participants who are progressing on combination ipilimumab/nivolumab as their last line of therapy

Lab requirements

Blood counts

Leukocytes ≥3,000/mcL; Absolute neutrophil count ≥1,000/mcL; Platelets ≥75,000/mcL

Kidney function

CrCL > 30 ml/min

Liver function

Total bilirubin ≤3 institutional ULN; AST(SGOT)/ALT(SGPT) ≤5 × institutional ULN

Participants must have adequate organ and marrow function as defined below: * Leukocytes ≥3,000/mcL * Absolute neutrophil count ≥1,000/mcL * Platelets ≥75,000/mcL * Total bilirubin ≤3 institutional upper limit of normal (ULN) * AST(SGOT)/ALT(SGPT) ≤5 × institutional ULN * CrCL > 30 ml/min

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Massachusetts General Hospital Cancer Center · Boston, Massachusetts

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See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05779423 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior combination checkpoint inhibitor disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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Related pages

Melanoma trials