RecruitingPhase 4NCT06116461

Nivolumab Dose Optimization in Patients With a Complete, Partial or Stable Response


Sponsor

Erasmus Medical Center

Enrollment

34 participants

Start Date

Jan 5, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Patients with advanced melanoma are, amongst others, currently treated with nivolumab monotherapy or with nivolumab and ipilimumab followed by nivolumab. Even though registration studies administered nivolumab in a 3 mg/kg 2 weekly scheme, currently, nivolumab monotherapy is either administered in a 240 mg 2-weekly scheme or in a 6 mg/kg or 480 mg 4-weekly scheme. With the current dosing regimen, steady-state is achieved after approximately 5 to 6 months, whereas a tumour response is usually observed earlier in patients with metastatic melanoma. Moreover, PD-1 receptor occupancy is almost saturated above doses of 0.3 mg/kg, or at nivolumab serum levels of 10 mg/L, which is a concentration that is achieved after one treatment cycle. In melanoma patients, the additional probability on response in patients treated with 3 mg/kg compared to 1 mg/kg seems limited. PFS and OS for 3 mg/kg were not superior to 1 mg/kg. Therefore, in this study, our aim is to investigate nivolumab trough levels and pharmacokinetic parameters after 3 reduced nivolumab doses.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study looks at whether patients with advanced melanoma (skin cancer) who are responding well to nivolumab (an immunotherapy drug) can safely reduce their dose without losing effectiveness. The goal is to find the lowest dose that still works, which could reduce side effects and costs. **You may be eligible if:** - You are 18 or older - You have advanced or metastatic melanoma - You are currently being treated with nivolumab at a standard dose (6 mg/kg or 480 mg every 4 weeks) - Your cancer has had a complete response, partial response, or stable disease for at least 6 months **You may NOT be eligible if:** - You cannot have blood drawn for study purposes - You are enrolled or wish to enroll in the SAFE-STOP trial Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGNivolumab

Participants receive three reduced doses of 240 mg every four weeks


Locations(1)

Erasmus MC

Rotterdam, Pending, Netherlands

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NCT06116461


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