Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

0.0%

0 terminated/withdrawn out of 14 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

29%

4 trials in Phase 3/4

Results Transparency

0%

0 of 13 completed trials have results

Key Signals

Enrollment Performance

Analytics

Phase 1
5(35.7%)
Phase 2
4(28.6%)
Phase 3
4(28.6%)
N/A
1(7.1%)
14Total
Phase 1(5)
Phase 2(4)
Phase 3(4)
N/A(1)

Activity Timeline

Global Presence

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Clinical Trials (14)

Showing 14 of 14 trials
NCT05279846Phase 3Active Not Recruiting

A Vehicle-controlled Study of Topical MOB015B in the Treatment of Distal Subungual Onychomycosis (DSO)

Role: lead

NCT06369675Phase 1Completed

Skin Irritation Potential of MOB015B in Healthy Subjects Using a Cumulative Irritant Patch Test Design

Role: lead

NCT06369727Phase 1Completed

Study to Evaluate the Sensitizing Potential of MOB015B in Healthy Subjects Using a Repeat Insult Patch Test Design

Role: lead

NCT02859519Phase 3Completed

A Multi-centre, Double-blind, Randomized, Vehicle-controlled Study of Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)

Role: lead

NCT02866032Phase 3Completed

Study to Evaluate the Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)

Role: lead

NCT03244280Phase 1Completed

A Study of the Systemic Absorption of MOB015B

Role: lead

NCT01814020Phase 2Completed

An Open,Single-centre Pilot Study of Efficacy and Safety of Topical MOB015B in the Treatment of Distal Subungual Onychomycosis (DSO)

Role: lead

NCT01611480Phase 2Completed

Efficacy and Safety of a New Topical Formulation With Imiquimod (Limtop) Applied 1, 3 or 7 Times Weekly During 2 x 2 Weeks Treatment for Actinic Keratosis on the Head

Role: lead

NCT01180491Not ApplicableCompleted

A Clinical Investigation on Early Visible Effects of Application of K101 During 8 Weeks on Discoloured and Deformed Nails Resulting From Onychomycosis

Role: lead

NCT01246518Phase 2Completed

Efficacy and Safety of Two Treatment Regimens of Topical MOB015 in Adults With Distal Subungual Onychomycosis

Role: lead

NCT01567683Phase 1Completed

A Double-blind, Randomized, Single Centre, Vehicle-controlled Study to Evaluate the Safety and Tolerability of a New Topical Formulation Containing 0,09% Imiquimod (Limtop) in Healthy Subjects

Role: lead

NCT01137331Phase 3Completed

K301 for the Treatment of Seborrhoeic Eczema (SE) of the Scalp

Role: lead

NCT01137630Phase 2Completed

Two Topical K40 Formulations in Adults With Seborrhoeic Dermatitis (SD) of the Scalp

Role: lead

NCT00863005Phase 1Completed

Assessment of the Effects on Barrier Impairment, Clinical Features and Bacterial Colonization of Topical Formulations in Patients With Atopic Eczema; a Phase IIa, Single-center, Randomized, Observer-blind Study

Role: lead

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