Skin Abnormalities: Clinical Trials

6 trials for Skin Abnormalities, newest first

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6 terminated. 6 Phase 3, 2 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 36Terminated 6
Phase 22Terminated 2

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Trials (filtered) newest first · largest first

All 6 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Study to Test Whether Spesolimab Helps People With a Skin Disease Called Netherton Syndrome
Spesolimab - solution for infusion, Placebo matching to spesolimab - solution for infusion, Spesolimab - solution for injection - Netherton Syndrome
Phase 2 / Phase 3TerminatedBoehringer Ingelheim432023-06-122026-03-12
A Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Syndrome
Dupilumab Prefilled Syringe, Placebo Prefilled Syringe - Netherton Syndrome
Phase 2 / Phase 3TerminatedUniversity Hospital, Toulouse102020-07-232026-09-21
Onreltea (Brimonidine) Gel In Pediatric Patients With Capillary Malformations
Brimonidine 0.33% gel - Capillary Malformations
Phase 3TerminatedThe Hospital for Sick Children62016-06-012019-04-16
Open Label Extension Study to Evaluate the Long-term Safety of Zorblisa (SD-101-6.0) in Patients With Epidermolysis Bullosa
SD-101-6.0 cream - Epidermolysis Bullosa
Phase 3TerminatedScioderm, Inc.1522015-06-092019-09-27
A Study of the Efficacy and Safety of ABH001 in the Treatment of Patients With Epidermolysis Bullosa Who Have Wounds That Are Not Healing
ABH001, Control wound treatment - Epidermolysis Bullosa
Phase 3TerminatedShire Regenerative Medicine, Inc.12012-12-012013-11-21
Safety and Efficacy of Apligraf in Nonhealing Wounds of Subjects With Junctional or Dystrophic Epidermolysis Bullosa (EB)
Apligraf, Standard dressing regimen - Epidermolysis Bullosa, Junctional, Epidermolysis Bullosa Dystrophica
Phase 3TerminatedOrganogenesis12007-12-012010-06-29

Narrower conditions

Epidermolysis Bullosa (2)  ·  Netherton Syndrome (2)  ·  Capillary Malformations, Congenital, 1 (1)  ·  Epidermolysis Bullosa Dystrophica (1)  ·  Epidermolysis Bullosa, Junctional (1)  ·  Port-Wine Stain (1)

Broader conditions

Congenital Abnormalities (6)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (6)  ·  Skin Diseases (6)  ·  Skin and Connective Tissue Diseases (6)  ·  Genetic Diseases, Inborn (5)  ·  Skin Diseases, Genetic (5)  ·  Skin Diseases, Vesiculobullous (3)  ·  Abnormalities, Multiple (2)  ·  Ichthyosiform Erythroderma, Congenital (2)  ·  Ichthyosis (2)  ·  Infant, Newborn, Diseases (2)  ·  Keratosis (2)  ·  Collagen Diseases (1)  ·  Connective Tissue Diseases (1)

Interventions

Brimonidine Tartrate (1)  ·  Gels (1)  ·  Injections (1)  ·  spesolimab (1)

Sponsors

Boehringer Ingelheim (1)  ·  Organogenesis (1)  ·  Scioderm, Inc. (1)  ·  Shire Regenerative Medicine, Inc. (1)  ·  The Hospital for Sick Children (1)  ·  University Hospital, Toulouse (1)

Countries

France (4)  ·  United States (4)  ·  Germany (3)  ·  Australia (2)  ·  Austria (2)  ·  Canada (2)  ·  Israel (2)  ·  Netherlands (2)  ·  Poland (2)  ·  Portugal (2)  ·  Spain (2)  ·  United Kingdom (2)  ·  Bulgaria (1)  ·  China (1)  ·  Italy (1)

Top investigators

Alan Arbuckle, MD, FAAD, FAAP (1)  ·  Damien Bates, MD, PhD, FRACS (Plast.) (1)  ·  Elena Pope, MD (1)  ·  Elizabeth Alvarez- Connelly, MD (1)

NIH funding

2014 (1)