An Open Trial to Assess the Tolerability of AVANZ® Cupressus Immunotherapy

Status Completed

Clinical Trial Summary

This trial is an open, national, multi-centre trial. The main objective of this trial is to assess the tolerability of the up-dosing phase of AVANZ® Cupressus arizonica by measurement of related Adverse Events.

Clinical Trial Description

The main objective of this trial is to assess the tolerability of the up-dosing phase of AVANZ® Cupressus arizonica, the measurement rate is the frequency of patients with investigational medicinal product (IMP)-related adverse events (AEs) will be the primary endpoint. ;

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02069535
Study type	Interventional
Source	ALK-Abelló A/S
Contact
Status	Completed
Phase	Phase 2
Start date	April 2014
Completion date	November 2014

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