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

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

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06116461
Acronym
NIVOPTIMIZE
Enrollment
34
Registered
2023-11-03
Start date
2022-01-05
Completion date
2025-01-31
Last updated
2024-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma

Brief 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.

Interventions

DRUGNivolumab

Participants receive three reduced doses of 240 mg every four weeks

Sponsors

Erasmus Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Advanced or metastatic melanoma * Current treatment with nivolumab for advanced or metastatic melanoma, in a 6 mg/kg or 480 mg, 4 weekly scheme * Documented confirmed and ongoing CR, PR or SD according to RECIST v1.1 * On treatment for at least 6 months

Exclusion criteria

* Unable to draw blood for study purposes * Patients willing to participate or already included in the SAFE-STOP trial

Design outcomes

Primary

MeasureTime frameDescription
Difference between the nivolumab mean trough level after 3 reduced doses (240 mg every 4 weeks) and after the first dose of 6 mg/kg or 480 mg.Through study completion, an average of four monthsDifference between the nivolumab mean trough level after 3 reduced doses (240 mg every 4 weeks) and after the first dose of 6 mg/kg or 480 mg.

Secondary

MeasureTime frameDescription
- PD-1 receptor occupancy in PBMCs, measured 4 weeks after 3 reduced nivolumab dosesThrough study completion, an average of four months\- PD-1 receptor occupancy in PBMCs, measured 4 weeks after 3 reduced nivolumab doses
Grade ≥3 adverse events (CTCAE) during reduced dosesThrough study completion, an average of four monthsGrade ≥3 adverse events (CTCAE) during reduced doses
Number of patients with new PD during 3 reduced dosesThrough study completion, an average of four monthsNumber of patients with new PD during 3 reduced doses

Countries

Netherlands

Contacts

Primary ContactMichiel Zietse, MSc
michielzietse@gmail.com+31642534225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026