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/ Moberg Pharma AB
Moberg Pharma AB
Industry · 14 registered clinical trials.
Status
Trial
Phase
Started
Active Not Recruiting
A Vehicle-controlled Study of Topical MOB015B in the Treatment of Distal Subungual Onychomycosis (DSO)
Onychomycosis
Phase 3
2022-05-09
Completed
A Study of the Systemic Absorption of MOB015B
Onychomycosis
Phase 1
2017-12-16
Completed
Skin Irritation Potential of MOB015B in Healthy Subjects Using a Cumulative Irritant Patch Test Design
Erythema
Phase 1
2017-10-19
Completed
Study to Evaluate the Sensitizing Potential of MOB015B in Healthy Subjects Using a Repeat Insult Patch Test De
Erythema
Phase 1
2017-10-15
Completed
A Multi-centre, Double-blind, Randomized, Vehicle-controlled Study of Efficacy and Safety of Topical MOB015B i
Distal Subungual Onychomycosis
Phase 3
2016-10-01
Completed
Study to Evaluate the Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subun
Distal Subungual Onychomycosis
Phase 3
2016-09-01
Completed
An Open,Single-centre Pilot Study of Efficacy and Safety of Topical MOB015B in the Treatment of Distal Subungu
Distal Subungual Onychomycosis
Phase 2
2012-12-01
Completed
Efficacy and Safety of Two Treatment Regimens of Topical MOB015 in Adults With Distal Subungual Onychomycosis
Onychomycosis
Phase 2
2010-12-01
Completed
A Clinical Investigation on Early Visible Effects of Application of K101 During 8 Weeks on Discoloured and Def
Onychomycosis
N/A
2010-09-01
Completed
K301 for the Treatment of Seborrhoeic Eczema (SE) of the Scalp
Seborrhoeic Eczema of the Scalp
Phase 3
2008-02-01
Completed
Two Topical K40 Formulations in Adults With Seborrhoeic Dermatitis (SD) of the Scalp
Seborrhoeic Dermatitis of the Scalp
Phase 2 / Phase 3
2007-02-01
Completed
A Double-blind, Randomized, Single Centre, Vehicle-controlled Study to Evaluate the Safety and Tolerability of
Healthy
Phase 1
—
Completed
Assessment of the Effects on Barrier Impairment, Clinical Features and Bacterial Colonization of Topical Formu
Atopic Dermatitis
Phase 1 / Phase 2
—
Completed
Efficacy and Safety of a New Topical Formulation With Imiquimod (Limtop) Applied 1, 3 or 7 Times Weekly During
Actinic Keratosis
Phase 2
—