Last reviewed · How we verify
NCT03094845
Safety and Clinical Tolerability of hdmASIT+TM Peptides Administered in HDM-induced Allergic Patients
Phase 2 trial testing Placebo solution in House Dust Mite Allergy in 36 participants. Completed in 23 January 2017.
12 January 2017
Quick facts
| Lead sponsor | ASIT Biotech S.A. |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 36 |
| Start date | 28 September 2016 |
| Primary completion | 12 January 2017 |
| Estimated completion | 23 January 2017 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- Placebo solution
- hdmASIT+TM — full drug profile →
Conditions studied
- House Dust Mite Allergy — all drugs for House Dust Mite Allergy →
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.
Verify or expand the search:
- PubMed search for NCT03094845
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for House Dust Mite Allergy
Currently open trials in the same condition.
- NCT06920771 — A Randomized, Double-Blind, Placebo-Controlled, Multi-Centre Study to Assess the Efficacy of PURETHAL Mites Mixture 50,0 · Phase 3 · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03094845 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by ASIT Biotech S.A.
- Last refreshed: 29 March 2017
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing