WHO ICTRP trial

Estudio fase II randomizado de Capecitabina + Bevacizumab versus Capecitabina +…

EUCTR2009-010192-24-ES · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2009-010192-24-ES
Public title Estudio fase II randomizado de Capecitabina + Bevacizumab versus Capecitabina + Oxaliplatino + Bevacizumab en combinación con radioterapia externa como tratamiento preoperatorio en pacientes con cáncer rectal localmente avanzado resecable - AVAROX
Scientific title Estudio fase II randomizado de Capecitabina + Bevacizumab versus Capecitabina + Oxaliplatino + Bevacizumab en combinación con radioterapia externa como tratamiento preoperatorio en pacientes con cáncer rectal localmente avanzado resecable - AVAROX
Primary sponsor Grupo de Tratamiento de los Tumores Digestivos (TTD)
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Spain
Conditions cáncer rectal localmente avanzado resecable MedDRA version: 9 Level: LLT Classification code 10038038 Term: Rectal cancer
Interventions Trade Name: AVASTIN 25 mg/ml concentrado para solución para perfusión Pharmaceutical Form: Concentrate for solution for infusion INN or Proposed INN: BEVACIZUMAB Other descriptive name: BEVACIZUMAB Concentration unit: mg/ml…
Registration date Mar 31, 2009
Secondary IDs TTD-08-05
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