Key Insights

Highlights

Success Rate

98% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

1.9%

1 terminated out of 53 trials

Success Rate

97.9%

+11.4% vs benchmark

Late-Stage Pipeline

26%

14 trials in Phase 3/4

Results Transparency

17%

8 of 46 completed with results

Key Signals

8 with results98% success

Data Visualizations

Phase Distribution

39Total
Not Applicable (4)
Early P 1 (1)
P 1 (3)
P 2 (17)
P 3 (12)
P 4 (2)

Trial Status

Completed46
Recruiting4
Unknown2
Terminated1

Trial Success Rate

97.9%

Benchmark: 86.5%

Based on 46 completed trials

Clinical Trials (53)

Showing 20 of 20 trials
NCT07427576Completed

Retrospective Study Evaluating the Effectiveness and Safety of Immunotherapy With Clustoid Max Forte

NCT07348302Phase 3Recruiting

Efficacy and Safety of SLIT in Patients With Rhinitis/RC With/Without Mild-moderate Asthma, Due to Dpt and/or Df

NCT06448585Phase 4Completed

Dietary Supplement (Beta-Glucans) in Allergic Patients Undergoing Subcutaneous Immunotherapy.

NCT05560698Not ApplicableCompleted

A Motivation-enhancing App to Retain Patients With Hay Fever in a Trial After Treatment

NCT05960266Early Phase 1Completed

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

NCT04898283Phase 3Recruiting

Efficacy and Safety Evaluation of the Treatment of Allergy Against Cupressaceae and Grasses.

NCT04435990Phase 3Recruiting

Efficacy and Safety Evaluation for the Treatment of Allergy Against Mites

NCT04891237Phase 3Recruiting

Efficacy and Safety Evaluation for the Treatment of Allergy Against Grass and Olive Pollen

NCT05540717Phase 3Completed

Efficacy and Safety of PQ Grass in Subjects With Seasonal Allergic Rhinitis and/or Rhinoconjunctivitis Induced by Grass Pollen

NCT04476433Not ApplicableCompleted

Intervention in Chronic Pediatric Patients and Their Families.

NCT02654223Phase 2Completed

Dose Finding for the Treatment of Rhinitis/Rhinoconjunctivitis Against Grass Pollen Allergy

NCT03821077Completed

Study to Evaluate the Efficacy and Safety of "Allergovac Poliplus" in Polysensitized Patients With Allergic Rhinitis/Rhinoconjunctivitis, With or Without Asthma

NCT04583202Not ApplicableCompleted

Evaluation of the Nasal and Conjunctival Response in Subjects Allergic to Birch Pollen in the ALYATEC Environmental Exposure Chamber

NCT02661854Phase 2Unknown

Dose Finding for the Treatment of Rhinitis/Rhinoconjunctivitis Against Mite Allergy

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)

NCT02844842Completed

Evaluation of Tolerability and Safety of "Allergovac Poliplus" in Polysensitized Patients With Rhinitis or Allergic Rhinoconjunctivitis With or Without Asthma: A Study in Daily Clinical Practice

NCT03414801Not ApplicableCompleted

Red Maple Trials Cat Allergen Natural Exposure Chamber Validation in Cat-allergic Subjects

NCT02340130Phase 2Completed

Safety, Tolerability and Efficacy of the Depigmented Modified Allergen Extract of Two Mites in Subjects With Allergic Rhinitis or Rhinoconjunctivitis, With Controlled Allergic Asthma

NCT01620762Phase 3CompletedPrimary

Phase III Cat-PAD Study

NCT02150343Phase 2CompletedPrimary

Phase II HDM-SPIRE Safety and Efficacy Study

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