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NCT02477917

A Multicenter, Open Clinical Trial With Subcutaneous Immunotherapy in Depot in Patients With Rhinoconjunctivitis Sensitized to Parietaria Judaica

Completed Phase 1 Last updated 28 April 2017
What this trial tests

Phase 1 trial testing Allergovac depot with Parietaria judaica pollen extract in Rhinoconjunctivitis in 51 participants. Completed in 1 March 2016.

Timeline
1 May 2015
Primary endpoint
1 March 2016
1 March 2016

Quick facts

Lead sponsorRoxall Medicina España S.A
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment51
Start date1 May 2015
Primary completion1 March 2016
Estimated completion1 March 2016
Sites4 locations across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Roxall Medicina España S.A — full company profile →

Who can join

Adults 18 to 60, any sex, with Rhinoconjunctivitis. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The study was designed according to the draft of allergenic product regulation published by Spanish Regulatory Agency. The aim of the study is to evaluate the safety and tolerability of subcutaneous immunotherapy with Parietaria judaica pollen extract in patients with rhinoconjunctivitis with or without associated mild asthma. In addition, surrogate efficacy parameters will be evaluated: immunoglobulin level changes and skin reactivity.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Roxall Medicina España S.A trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02477917.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing