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RECRUITING
NCT06116461
PHASE4

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

Sponsor: Erasmus Medical Center

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

34

Start Date

2022-01-05

Completion Date

2025-01

Last Updated

2024-04-22

Healthy Volunteers

No

Conditions

Interventions

DRUG

Nivolumab

Participants receive three reduced doses of 240 mg every four weeks

Locations (1)

Erasmus MC

Rotterdam, Pending, Netherlands