CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 11 enrolled
Drug / intervention
Bintrafusp alfa/M7824 +9 moredrug
Likely dose
Bintrafusp alfa/M7824 1200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05012098
NCT05012098Phase 2Completed

Phase 2 Study of Bintrafusp Alfa in Recurrent/Metastatic Olfactory Neuroblastoma (BARON).

National Cancer Institute (NCI)·interventional·Posted Aug 19, 2021·Updated Aug 8, 2025

In Brief

A Phase 2 clinical trial evaluating Bintrafusp alfa/M7824, Ibuprofen, and 8 other interventions for Olfactory Neuroblastoma and 2 related conditions. Completed, enrolled 11 participants across 1 site.

Detailed Summary

Background: Olfactory neuroblastoma (ONB) is a rare cancer of the nasal cavity. At diagnosis, it is usually locally advanced. It tends to spread to the neck. Sometimes it spreads to the lungs and bones. Researchers want to find a better way to treat it. Objective: To learn if giving immunotherapy drug bintrafusp alfa can help ONB shrink or disappear. Eligibility: People aged 18 years and older diagnosed with recurrent or metastatic ONB that has not responded to standard treatment. Design: Participants will be screened with a medical history, blood and urine tests, and physical exam. Their ability to perform their normal activities will be assessed. They will have an electrocardiogram to evaluate their heart. They will have imaging scans and/or a nuclear bone scan, as needed. For some scans, they may receive a contrast dye. Some screening tests will be repeated during the study. Participants will receive bintrafusp alfa once every 2 weeks for 26 doses. They will get it intravenously over 60 minutes. They may get other medicines to prevent side effects. They will complete health questionnaires. Visits will last 4-6 hours. Participants may have optional tumor biopsies. Participants will have an end of treatment visit within 7 days after they stop taking the study drug. About 28 days after treatment ends, they will have a safety visit. They will have follow-up visits every 3 months for the first year, then every 6 months for years 2-5, and then once a year after that for the rest of their life. If their disease progresses, they may be eligible for re-treatment with the study drug

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20222023202420252026
First PostedAug 19, 2021
Enrollment StartJun 21, 2022
Primary CompletionJul 9, 2024
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 4.9 years ago

Interventions

Bintrafusp alfa/M7824drug

Participants will be treated with bintrafusp alfa 1200 mg every 2 weeks for 26 doses.

Ibuprofendrug

400 mg or comparable non-steroidal anti-inflammatory drugs (NSAIDs) dose up to 2 hours before and 8 hours after the start of each dose for prophylaxis of flu-like symptoms.

PET scanother

Screening

CT scanother

Screening

Tumor tissue biopsyprocedure

Baseline, and subsequent weeks as stipulated in the study calendar.

Brain MRIother

Baseline

Dotate scanother

Baseline

PET FDG scanother

Baseline

Nuclear bone scanother

Baseline

EKGother

Baseline