Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

5.3%

1 terminated/withdrawn out of 19 trials

Success Rate

94.4%

+7.9% vs industry average

Late-Stage Pipeline

42%

8 trials in Phase 3/4

Results Transparency

12%

2 of 17 completed trials have results

Key Signals

2 with results

Enrollment Performance

Analytics

Phase 3
8(42.1%)
Phase 2
7(36.8%)
Phase 1
4(21.1%)
19Total
Phase 3(8)
Phase 2(7)
Phase 1(4)

Activity Timeline

Global Presence

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Clinical Trials (19)

Showing 19 of 19 trials
NCT05788497Phase 3Terminated

Efficacy and Safety of Hemorrane Plus Versus Hemorrane and Versus Placebo in Patients With Uncomplicated Haemorrhoids

Role: lead

NCT06176560Phase 3Unknown

Phase III Multicentre Trial of Oral Mesalazine in Patients With Mild to Moderate Ulcerative Colitis.

Role: lead

NCT04735926Phase 2Completed

Efficacy and Safety of Calcifediol vs Placebo in Subjects With Vitamin D Deficiency

Role: lead

NCT03231969Phase 2Completed

A Single-Center, Phase 2 Study Evaluating Bilastine Ophthalmic Solution in the CAC® Model

Role: lead

NCT04810390Phase 3Completed

Study to Assess the Safety, Tolerability and Efficacy of Bilastine Ophthalmic Solution 0.6% in Children

Role: lead

NCT03479307Phase 3Completed

A Study Evaluating Bilastine Ophthalmic Solution 0.6% in the Conjunctival Allergen Challenge (Ora-CAC®) Model.

Role: lead

NCT04366908Phase 2Completed

Prevention and Treatment With Calcifediol of COVID-19 Induced Acute Respiratory Syndrome

Role: collaborator

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

Role: lead

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)

Role: lead

NCT00572611Phase 1Completed

Human Mass Balance Study With Bilastine

Role: lead

NCT01081574Phase 1Completed

Pharmacokinetic Study of Bilastine in Children From 2 to < 12 Years of Age With Either Allergic Rhinoconjunctivitis (AR) or Chronic Urticaria (CU)

Role: lead

NCT01124123Phase 1Completed

Oral Bioavailability of Bilastine

Role: lead

NCT01127620Phase 3Completed

Efficacy Study for the Symptomatic Treatment of Perennial Allergic Rhinitis With a 1 Year Safety Extension

Role: lead

NCT01271075Phase 2Completed

Bilastine Updosing - Characterization of Underlying Mechanisms

Role: collaborator

NCT00420082Phase 2Completed

A Randomized, Double-Blind, 4-way Crossover Study to Evaluate the Efficacy of Bilastine in the Vienna Challenge Chamber

Role: lead

NCT00419783Phase 1Completed

A Randomized, Multiple Dose, Double Blind, 5-way Crossover Study of the Electrocardiographic (ECG) Effects of Bilastine

Role: lead

NCT01108783Phase 3Completed

A Phase III Efficacy Study of the Symptomatic Treatment of Seasonal Allergic Rhinitis With Bilastine

Role: lead

NCT00504933Phase 3Completed

Efficacy Study for the Symptomatic Treatment of Seasonal Allergic Rhinitis

Role: lead

NCT00421109Phase 3Completed

Efficacy Study for the Symptomatic Treatment of Chronic Idiopathic Urticaria

Role: lead

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