WHO ICTRP trial

A clinical study conducted in several test centres to investigate the safety and…

EUCTR2015-002409-13-DE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2015-002409-13-DE
Public title A clinical study conducted in several test centres to investigate the safety and tolerability of a year-round dosage of immune therapy with an Allergoid drug in patients with hay fever and or without controlled asthma.
Scientific title A multicenter, randomized, open-label clinical trial to evaluate safety and tolerability of a year-round initiation of specific immunotherapy with an aluminum hydroxide adsorbed allergoid preparation of 6-grasses in patients with moderate to severe seasonal rhinitis or rhinoconjunctivitis with or…
Primary sponsor Allergopharma GmbH & Co. KG
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): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries Germany
Conditions Patients with moderate to severe seasonal rhinitis or rhinoconjunctivitis with or without controlled asthma. MedDRA version: 19.0 Level: LLT Classification code 10039776 Term: Seasonal allergic rhinitis System Organ Class: 100000004870…
Interventions Trade Name: Allergovit® Grasses Product Name: Allergovit® Grasses Product Code: 553a/91a-b Pharmaceutical Form: Suspension for injection INN or Proposed INN: Allergovit® grasses CAS Number: 8000045-25-2 Other descriptive name: ALLERGENS…
Registration date Aug 28, 2015
Target size 240
Secondary IDs AL1501AV
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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