WHO ICTRP trial

Nivolumab in combination with temozolomide and radiotherapy in children and…

EUCTR2018-002688-24-FR · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2018-002688-24-FR
Public title Nivolumab in combination with temozolomide and radiotherapy in children and adolescents with newly diagnosed high-grade glioma
Scientific title Phase I-II study of nivolumab in combination with temozolomide and radiotherapy in children and adolescents with newly diagnosed high-grade glioma - NIVOGLIO
Primary sponsor Gustave Roussy
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): yes Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries France;Italy;United Kingdom
Conditions Newly diagnosed High-Grade Gliomas (HGG) MedDRA version: 20.0 Level: PT Classification code 10065443 Term: Malignant glioma System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) MedDRA version…
Interventions Product Name: Nivolumab Product Code: BMS-936558 Pharmaceutical Form: Solution for infusion INN or Proposed INN: Nivolumab Other descriptive name: NIVOLUMAB Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal…
Registration date Feb 20, 2019
Target size 40
Secondary IDs 2018/2797
Registry page clinicaltrialsregister.eu

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations