Evaluation of the Safety and Pharmacokinetics of Dinutuximab Beta As Maintenance Therapy in Chinese Participants With High-Risk Neuroblastoma

PHASE1CompletedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

June 7, 2022

Primary Completion Date

June 29, 2023

Study Completion Date

June 29, 2023

Conditions
High-risk Neuroblastoma
Interventions
DRUG

Dinutuximab Beta

Dinutuximab beta was administered intravenously at a dosage of 10 milligrams/ meters squared (mg/m2) per day for 10 consecutive days

DRUG

13-cis-Retinoic Acid

13-cis-Retinoic Acid was administered orally at a daily total dose of 160 mg/m2, divided into approximately two equal doses given twice daily for 14 days following the conclusion of dinutuximab beta infusion.

Trial Locations (3)

Unknown

Xinhua Hospital Affiliated To Shanghai Jiao Tong University School Of Medicine, Shanghai

Tianjin Medical University Cancer Institute & Hospital, Tianjin

The Children's Hospital Zhejiang University School of Medicine, Hangzhou

Sponsors

Lead Sponsor

All Listed Sponsors
lead

BeiGene

INDUSTRY