Pilot Study Evaluating the Efficacy of a Topical PDE4 Inhibitor for Morphea
NCT03351114 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 8
Last updated 2021-04-01
Summary
This is a pilot study to determine the safety and clinical efficacy of crisaborole 2% ointment in the treatment of morphea.
Conditions
- Morphea
Interventions
- DRUG
-
Crisaborole
Apply Crisaborole 2% ointment to affected skin twice per day.
Sponsors & Collaborators
- collaborator INDUSTRY
- lead OTHER
Principal Investigators
-
Adela Cardones, MD · Duke UMC
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-09-01
- Primary Completion
- 2020-03-10
- Completion
- 2020-03-10
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Variegate Porphyria (VP)
NCT05854784 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, PK/PD, and Exploratory Efficacy Study of AMT-191 in Classic Fabry Disease
NCT06270316 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of CDX 6114 in PKU Patients
NCT04256655 ·Status: WITHDRAWN ·Phase: PHASE1
-
An Efficacy and Safety Study of Palovarotene for the Treatment of MO
NCT03442985 ·Status: TERMINATED ·Phase: PHASE2
-
A Study of PTC923 (CNSA-001) in Primary Tetrahydrobiopterin (BH4) Deficient Participants With Hyperphenylalaninemia
NCT03519711 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study of Intrathecal SHP611 in Children With Metachromatic Leukodystrophy
NCT03771898 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Phase 3 Study to Evaluate the Efficacy & Safety of Self-Administered Injections of BMN165 by Adults With PKU
NCT01889862 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Acamprosate in Fragile x Syndrome
NCT01911455 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Tolerability Study of rAvPAL-PEG to Treat Phenylketonuria
NCT00634660 ·Status: COMPLETED ·Phase: PHASE1
-
Oral Epalrestat Therapy in Pediatric Subjects With PMM2-CDG
NCT04925960 ·Status: TERMINATED ·Phase: PHASE3
-
A Study of BPN14770 in Male Adults (Aged 18 to 45) With Fragile X Syndrome
NCT05358886 ·Status: COMPLETED ·Phase: PHASE3
-
Pharmacokinetics and Safety Study of Single and Multiple Oral Doses Prodarsan™ in Patients With Cockayne Syndrome
NCT01142154 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Multi-Country Observational Study of Safety and Effectiveness of Elfabrio® in Fabry Patients
NCT06663358 ·Status: RECRUITING
-
An Open-Label Extension Study for Patients With Duchenne Muscular Dystrophy Who Participated in Studies of SRP-5051 (Vesleteplirsen)
NCT03675126 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
A Study of Sepiapterin in Participants With Phenylketonuria (PKU)
NCT06302348 ·Status: RECRUITING ·Phase: PHASE3
-
A Study of Pitolisant in Participants With Prader-Willi Syndrome
NCT07219485 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE3
-
A Dose-finding Study to Evaluate mRNA-3210 in Participants With Phenylketonuria
NCT06147856 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2
-
The Safety and Efficacy of Intravenous EXG110 in Patients With Fabry Disease
NCT06819514 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
Clinical Study of Aldurazyme in Patients With Mucopolysaccharidosis (MPS) I
NCT00912925 ·Status: COMPLETED ·Phase: PHASE3
-
A First-in-Human Phase 1 Study of Plasmalogen Precursor PPI-1011 in Healthy Adult Volunteers to Assess Safety, Tolerability, and Pharmacokinetics
NCT05969977 ·Status: UNKNOWN ·Phase: PHASE1
-
Study to Evaluate the Safety and Efficacy of Pegvaliase in Adolescents (Ages 12-17) With Phenylketonuria
NCT05270837 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Study of the Safety and Biologic Activity of AL01211 in Treatment Naive Males With Classic Fabry Disease
NCT06114329 ·Status: RECRUITING ·Phase: PHASE2
-
Clinical Study of QRX003 Lotion in Subjects With Netherton Syndrome
NCT06953466 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
Clinical Characterization on PDE6A-related Retinitis Pigmentosa in Preparation to a Gene Therapy Trial
NCT02759952 ·Status: COMPLETED
-
Oral Pirfenidone for the Pulmonary Fibrosis of Hermansky-Pudlak Syndrome
NCT00001596 ·Status: COMPLETED ·Phase: PHASE2