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Completed Phase 1 Interventional

A Study of TB-403 in Pediatric Subjects With Relapsed or Refractory Medulloblastoma

ClinicalTrials.gov ID: NCT02748135

Public ClinicalTrials.gov record NCT02748135. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 8, 2026, 3:22 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Open-Label, Multicenter, Dose Escalation Study of TB-403 in Pediatric Subjects With Relapsed or Refractory Medulloblastoma, Neuroblastoma, Ewing Sarcoma or Alveolar Rhabdomyosarcoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety and tolerability profile of TB-403 (humanized monoclonal antibody against placental growth factor (PlGF)) in pediatric subjects with relapsed or refractory Medulloblastoma.

Study identification

NCT ID
NCT02748135
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Oncurious NV
Industry
Enrollment
18 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Months to 18 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2016 (Type not available)
Primary completion
Oct 6, 2020 (Actual)
Completion
Oct 6, 2020 (Actual)
Last update posted
Jan 13, 2021

2016 – 2020

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Not listed Little Rock Arkansas 72202 —
Not listed Oakland California 94609 —
Not listed Hartford Connecticut 06106 —
Not listed Boston Massachusetts 02115 —
Not listed Grand Rapids Michigan 49503 —
Not listed St Louis Missouri 63104 —
Not listed Hackensack New Jersey 07601 —
Not listed Charleston South Carolina 29425 —
Not listed Austin Texas 78723 —
Not listed Dallas Texas 75235 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02748135, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 13, 2021 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02748135 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →