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NCT07100704: Orion

Recurrent/Metastatic Olfactory Neuroblastoma: Evaluating the Efficacy and Safety of Nivolumab

Recruiting now Phase 2 Last updated 3 August 2025
What this trial tests

Phase 2 trial testing Nivolumab in Recurrent/ Metastatic Olfactory Neuroblastoma in 14 participants. Currently enrolling.

Timeline
15 April 2025
Primary endpoint
14 April 2028
14 October 2028

Quick facts

Lead sponsorNational Cancer Center Hospital East
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment14
Start date15 April 2025
Primary completion14 April 2028
Estimated completion14 October 2028
Sites2 locations across Japan

Drugs / interventions tested

Conditions studied

Sponsor

National Cancer Center Hospital East

Who can join

18 and older, any sex, with Recurrent/ Metastatic Olfactory Neuroblastoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This trial evaluates the efficacy and safety of nivolumab monotherapy in patients with recurrent or metastatic olfactory neuroblastoma that is difficult to treat with curative intent. Specifically, nivolumab 240 mg will be administered on Day 1 and Day 15 of each cycle, or nivolumab 480 mg will be administered on Day 1 of each cycle, and this will be continued until disease progression. One cycle is 28 days. The decision on which treatment to administer will be made through consultation between the participant in this trial and their attending physician.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Nivolumab

Trials testing the same drug.

Other National Cancer Center Hospital East trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07100704.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing