Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

3.8%

1 terminated/withdrawn out of 26 trials

Success Rate

95.8%

+9.3% vs industry average

Late-Stage Pipeline

73%

19 trials in Phase 3/4

Results Transparency

0%

0 of 23 completed trials have results

Key Signals

1 recruiting

Enrollment Performance

Analytics

Phase 3
15(60.0%)
Phase 2
6(24.0%)
Phase 4
4(16.0%)
25Total
Phase 3(15)
Phase 2(6)
Phase 4(4)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (26)

Showing 20 of 26 trials
NCT07096440Not Yet Recruiting

Noninterventional Study on Tolerability and Safety of One Strength Updosing With Novo-Helisen Depot House Dust Mites

Role: lead

NCT06778213Phase 4Recruiting

Evaluation of the Efficacy of Allergen-specific Immunotherapy Using Assessment in an Allergen Exposure chamber-a Randomized Placebo-controlled Double-blind Study

Role: collaborator

NCT02297490Phase 2Terminated

Evaluation of the Utility of an EEC for Assessing Efficacy of SIT in Pivotal Clinical Trials

Role: lead

NCT00841256Phase 3Completed

Multicenter Trial of Sublingual Immunotherapy With a Solution of Grass Pollen Allergen Extract in Children

Role: lead

NCT00263640Phase 3Completed

Safety and Efficacy of House Dust Mite Allergoid in the Treatment of Bronchial Asthma

Role: lead

NCT01353755Phase 3Completed

2nd Pivotal Study rPhleum - Adults and Adolescents With Rhinoconjunctivitis +/-Controlled Asthma

Role: lead

NCT00263627Phase 3Completed

Safety and Efficacy of Specific Immunotherapy With an Aluminium Hydroxide-adsorbed Allergoid Preparation of Birch Pollen Allergens

Role: lead

NCT00263601Phase 3Completed

Safety and Efficacy of Grass Pollen Allergoid in the Treatment of Allergic Rhinoconjunctivitis

Role: lead

NCT00264459Phase 3Completed

Safety and Efficacy of a Sublingual Specific Immunotherapy With an Extract of a Six Grass Pollen Mixture

Role: lead

NCT01490411Phase 2Completed

Dose Range Finding Study With rBet v1-FV - in Adult Patients With Birch Pollen-Allergic Seasonal Rhinoconjunctivitis

Role: lead

NCT00671268Phase 3Completed

Evaluation of Safety and Efficacy of Specific Immunotherapy With Recombinant Major Allergens of Timothy Grass Pollen Adsorbed Onto Aluminium-hydroxide in Patients With IgE-mediated Allergic Rhinoconjunctivitis +/- Controlled Asthma

Role: lead

NCT00666341Phase 2Completed

Dose-Response-Study With a Recombinant Cocktail of Phleum (rPhleum) Allergens

Role: lead

NCT00665483Phase 4Completed

Design of Optimally-diagnostic Skin Test Solutions for Diagnosis of Sensitisation to a Pollen and Dust Mite Mixture.

Role: lead

NCT00841516Phase 2Completed

Immunological and Histological Evaluation of Specific Immunotherapy With Recombinant Hypoallergenic Derivative

Role: lead

NCT00623701Phase 3Completed

Efficacy and Safety From a High-dosed Sublingual Grass Pollen Preparation

Role: lead

NCT00554983Phase 3Completed

Efficacy and Safety From a Recombinant Folding Variant of Bet v 1

Role: lead

NCT00263926Phase 3Completed

Efficacy and Safety of a Purified Standardised Wasp Venom Preparation

Role: lead

NCT00818181Phase 2Completed

Open Label Safety Study of a Birch Pollen Allergen Extract

Role: lead

NCT00309062Phase 3Completed

Safety and Efficacy of Recombinant Birch Pollen Allergen in the Treatment of Allergic Rhinoconjunctivitis

Role: lead

NCT00309036Phase 3Completed

Safety and Efficacy of Recombinant Grass Pollen Allergen Cocktail in the Treatment of Allergic Rhinoconjunctivitis

Role: lead