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Epidermolysis Bullosa clinical trials

View clinical trials related to Epidermolysis Bullosa.

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NCT ID: NCT04491604 Completed - Clinical trials for Recessive Dystrophic Epidermolysis Bullosa

Ph 3 Efficacy and Safety of B-VEC for the Treatment of DEB

GEM-3
Start date: August 17, 2020
Phase: Phase 3
Study type: Interventional

To determine whether administration of topical B-VEC improves wound healing as compared to placebo, and to evaluate durability, repeat dosing (Primary Endpoint) and further obtain safety and tolerability data.

NCT ID: NCT04227106 Completed - Clinical trials for Epidermolysis Bullosa

Phase 3, Open-label Clinical Trial of EB-101 for the Treatment of Recessive Dystrophic Epidermolysis Bullosa (RDEB)

Start date: January 10, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to evaluate safety and efficacy of surgical application of EB-101 (autologous, gene-corrected keratinocyte sheets) as a treatment of recessive dystrophic epidermolysis bullosa (RDEB).

NCT ID: NCT04217538 Completed - Clinical trials for Epidermolysis Bullosa

Observational Study of a Cohort of Patients With Hereditary Epidermolysis Bullosa

Start date: January 4, 2017
Phase:
Study type: Observational

Hereditary Epidermolysis Bullosa (EBH) are rare dermatologic diseases characterized by cutaneous and mucosa fragility. Oral manifestations of few small cohort have been published. The main objective of this multicentric cohort study first in Europe was to report the oral status of these patients that were consulted in the MRDRC of this disease in Nice (France), Toulouse (France) and Louvain (Belgium). Then a correlation between the oral characteristics and the EBH type will be made, in order to facilitate the management of patient care and the prevention program that can be established to improve their oral health.

NCT ID: NCT03942250 Completed - Clinical trials for Epidermolysis Bullosa

Uses of Irradiated Human Amniotic Membrane in the Treatment of Dystrophic Epidermolysis Bullosa Patients

Start date: January 2017
Phase: N/A
Study type: Interventional

To evaluate the effect of human amniotic membrane as a weekly dressing on chronic wounds in Epidermolysis Bullosa (EB) patients.

NCT ID: NCT03928093 Completed - Pain, Neuropathic Clinical Trials

Pregabalin Treatment for RDEB Pain and Itch

Start date: August 7, 2019
Phase: Phase 3
Study type: Interventional

Recessive dystrophic epidermolysis bullosa (RDEB) patients' quality of life is severely affected by neuropathic pain and itch, which have recently been demonstrated to be secondary to skin small fiber neuropathy. To date, there is no evidence on what the best agent is to control these symptoms. Based on the anecdotal data and safety profile, the investigators believe that pregabalin is a therapeutic agent that will be effective and safe in this population. The investigators propose to conduct a blinded study, using pregabalin versus placebo in which each patient serves as its own control (cross-over design). This is a feasibility study that will provide preliminary data on efficacy and safety of pregabalin in RDEB patients with neuropathic pain and itch and gather much needed data (dosage, titration schedule, outcome measures, etc) to inform the design of a larger cohort, controlled, multicenter trial.

NCT ID: NCT03836001 Completed - Clinical trials for Epidermolysis Bullosa

A Neurokinin-1 Receptor Antagonist for the Treatment of Pruritus in Patients With Epidermolysis Bullosa

Start date: April 18, 2019
Phase: Phase 2
Study type: Interventional

To determine if Serlopitant (when taken by mouth) is safe and works on itch in patients aged 13 and above with EB.

NCT ID: NCT03752905 Completed - Clinical trials for Recessive Dystrophic Epidermolysis Bullosa

A Phase 1/2 Trial of PTR-01 in Adult Patients With Recessive Dystrophic Epidermolysis Bullosa (RDEB)

PTR-01-001
Start date: January 9, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Protocol PTR-01-001 is a Phase 1/2 study of PTR-01. The study is divided into an up to 4-week Screening Period, a 10-week Treatment Period and an 8-week Follow-up Period. Cohorts 1, 2, 3 and 4 will consist of 2, 4, 3 and 3 patients respectively. Each cohort will consist of patients divided into two groups (Group 1 and Group 2) randomized in a 1:1 ratio. Patients in Group 1 will receive three doses of active drug followed by 3 doses of saline control. Patients in Group 2 will receive three doses of saline control followed by 3 doses of active drug. Cohort 1 patients randomized to Group 1 will receive 3 doses of active treatment (PTR-01) at a dose of 0.1 mg/kg followed by 3 doses of saline control for a total of 6 doses. Cohort 1 patients randomized to Group 2 will receive 3 doses of saline control followed by 3 doses of active treatment (PTR-01) at a dose of 0.1 mg/kg for a total of 6 doses.

NCT ID: NCT03730584 Completed - Clinical trials for Epidermolysis Bullosa

Evaluation of the Efficacy of ROPIVACAINE in Children and Young Adults With Hereditary Epidermolysis Bullosa

EBROPI
Start date: February 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether topical application of Ropivacaine is effective for treating refractory pain during dressing changes and so improve quality of life of patients (newborn, child, adolescent or adults under 21) suffering from hereditary epidermal epidermolysis bullosa.

NCT ID: NCT03536143 Completed - Clinical trials for Dystrophic Epidermolysis Bullosa

A Phase I/II Study of KB103, a Topical HSV1-COL7, on DEB Patients

GEM-1
Start date: May 6, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This study was conducted to assess the safety and efficacy of topical Beremagene Geperpavec (KB103, HSV1-COL7) on DEB patients.

NCT ID: NCT03529877 Completed - Clinical trials for Recessive Dystrophic Epidermolysis Bullosa

Allogeneic ABCB5-positive Stem Cells for Treatment of Epidermolysis Bullosa

Start date: February 16, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this clinical trial is to investigate the efficacy (by monitoring overall improvement of EB symptoms) and safety (by monitoring adverse events) of three doses of allo-APZ2-EB administered intravenously to patients with recessive dystrophic epidermolysis bullosa (RDEB).