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NCT03094845

Safety and Clinical Tolerability of hdmASIT+TM Peptides Administered in HDM-induced Allergic Patients

Completed Phase 2 Last updated 29 March 2017
What this trial tests

Phase 2 trial testing Placebo solution in House Dust Mite Allergy in 36 participants. Completed in 23 January 2017.

Timeline
28 September 2016
Primary endpoint
12 January 2017
23 January 2017

Quick facts

Lead sponsorASIT Biotech S.A.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment36
Start date28 September 2016
Primary completion12 January 2017
Estimated completion23 January 2017
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

ASIT Biotech S.A. — full company profile →

Who can join

Adults 18 to 64, any sex, with House Dust Mite Allergy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

hdmASIT+TM product is based on highly purified allergen fragments from house dust mites. The purpose of this study is to assess the safety and clinical tolerability of subcutaneous immunotherapy with hdmASIT+TM in patients with house dust mite-induced allergic rhinoconjunctivitis compared to placebo.

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 recruiting trials for House Dust Mite Allergy

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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/NCT03094845.

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