Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

0.0%

0 terminated out of 29 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

52%

15 trials in Phase 3/4

Results Transparency

7%

2 of 27 completed with results

Key Signals

2 with results100% success

Data Visualizations

Phase Distribution

27Total
Not Applicable (3)
Early P 1 (1)
P 1 (2)
P 2 (6)
P 3 (13)
P 4 (2)

Trial Status

Completed27
Unknown2

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 27 completed trials

Clinical Trials (29)

Showing 20 of 20 trials
NCT05960266Early Phase 1Completed

Immunological Analysis of Lymph Node Tissue After Intralymphatic Immunotherapy: A Prospective Case Control Study

NCT06457269Not ApplicableCompletedPrimary

Evaluating the Potential of Large Language Models for Respiratory Disease Consultations

NCT04622917Phase 4Completed

Methylprednisolone Injections Treating Birch Pollen Induced Allergic Rhinitis.

NCT04326309Completed

Audio Data Collection for Identification and Classification of Coughing

NCT01024608Phase 3Completed

Study in Adult and Adolescent Subjects With Seasonal Allergic Rhinitis (SAR)

NCT01660737CompletedPrimary

Observational Study With PASCALLERG ® in Patients With Hay Fever

NCT00574210Phase 2Completed

PK/PD and Steady State Efficacy Study of Bilastine Compared With Placebo Given Orally in the Treatment of the Symptoms of SAR in an EEC Model (5-arm)

NCT00574379Phase 2Completed

Efficacy, Safety and PK of Once or Twice Daily Bilastine (10 or 20 mg) Compared With Placebo in the Symptomatic Treatment of SAR

NCT00189917Phase 1Completed

Safety, Tolerability and Immune Response of IMVAMUNE (MVA-BN)Smallpox Vaccine in Patients With Atopic Disorders

NCT03724240Phase 3UnknownPrimary

Clinical Efficacy and Safety of Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis

NCT02560948Phase 3CompletedPrimary

Clinical Efficacy and Safety of a Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis

NCT02932774Phase 4Completed

Randomized, Double Blind, Parallel Group, Placebo Controlled, Multi-Center Study of the Efficacy and Safety of Cetirizine HCl Syrup vs. Loratadine Syrup vs. Placebo in Treatment of Children With Seasonal Allergic Rhinitis (SAR)

NCT00163488Phase 3Completed

Safety of Ciclesonide Nasal Spray Administered With Inhaled Fluticasone Dipropionate/Salmeterol in Adults With Perennial Allergic Rhinitis (BY9010/M1-409)

NCT00659594Phase 3Completed

Study Using the Environmental Exposure Chamber (EEC) to Assess the Onset of Action of Ciclesonide, Applied as a Nasal Spray in Treatment of Seasonal Allergic Rhinitis (BY9010/M1-406)

NCT00163514Phase 3Completed

Safety and Effectiveness of Ciclesonide Nasal Spray in Children (6 to 11 Years) With Perennial Allergic Rhinitis (BY9010/M1-403)

NCT00659841Phase 3Completed

To Assess the Safety and Efficacy of Ciclesonide, Applied as a Nasal Spray in the Treatment of Seasonal Allergic Rhinitis (BY9010/M1-401)

NCT00658918Phase 3Completed

To Assess the Safety of Ciclesonide, Applied as a Nasal Spray at Three Dose Levels, in the Treatment of Perennial Allergic Rhinitis in Pediatrics (BY9010/M1-405)

NCT00659503Phase 3Completed

Study Using the Environmental Exposure Unit (EEU) to Assess the Onset of Action of Ciclesonide, Applied as a Nasal Spray in the Treatment of Seasonal Allergic Rhinitis (BY9010/M1-407)

NCT00384475Phase 3Completed

A Study of Ciclesonide Nasal Spray in Patients 18 Years and Older With Seasonal Allergic Rhinitis (BY9010/M1-413)

NCT00261287Phase 3CompletedPrimary

Safety and Tolerability of Ciclesonide Nasal Spray in Patients With Perennial Allergic Rhinitis (2-5 Years Old) (BY9010/M1-416)

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