CACIPLIQ20 in Wound Healing in Subjects With Epidermolysis Bullosa
NCT06007235 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2024-02-13
Summary
Epidermolysis bullosa (EB) is a group of inherited disorders characterized by fragility of the skin and mucous membranes within the basement membrane zone. It is characterized by moderate to excessive fragility of epithelial tissues with prototypic blistering or erosions following minimal trauma (mechanobullous dermatoses). The chronic pain associated with EB, the hardship placed on caregivers, and the high risk for complications places a considerable psychosocial burden on both patients and their families. Despite considerable research to advance the understanding of EB pathophysiology, no treatments have been approved by regulatory authorities to date.
Heparan sulfates are key elements of the Extra Cellular Matrix scaffold which act both as linkers, bridging structural matrix proteins such as collagens, laminin and as storage and protector sites to communication peptides, playing a pivotal role in the regulation of cell proliferation, migration and differentiation that are all required for tissue regeneration and repair. CACIPLIQ20 is a bioengineered structural analogue of heparan sulfate glycosaminoglycans. Numerous experimental studies have provided strong evidence that CACIPLIQ20 promotes tissue regeneration by reconstructing the cellular microenvironment following tissue injury. CACIPLIQ20 is currently a class III CE marked medical device (NSAI-0050 CE MARK ECDECNL-A4 (6) and EC Annex II of the directive. NL-A4 (7)) with the following indications: Chronic ulcers showing no tendency to heal after 6 months of standard care, or still unhealed after 12 months:
* Pressure ulcers.
* Peripheral arterial disease (such as Stage IV Leriche \& Fontaine) ulcers.
* Diabetic ulcers (including amputation).
Preliminary results from several published and unpublished case reports (Al Malak and Barritault, 2012; Bodemer, unpublished observations) suggest that CACIPLIQ20 is safe and can improve wound healing and reduce pain in patients with epidermolysis bullosa.
The goal of the MATHBULL study is to confirm preliminary observations in a placebo-controlled double-blind pilot study. The results of this pilot study will help to design a pivotal study.
Conditions
- Epidermolysis Bullosa Dystrophica
- Epidermolysis Bullosa, Junctional
Interventions
- DEVICE
-
CACIPLIQ20
CACIPLIQ20 contains RGTA heparan sulphate mimetics
- DRUG
-
Saline solution in identical spray bottles
Sponsors & Collaborators
-
Euraxi Pharma
collaborator INDUSTRY -
ARANZ Medical
collaborator OTHER -
Organ, Tissue, Regeneration, Repair and Replacement
lead INDUSTRY
Principal Investigators
-
Christine Bodemer, MD, PhD · Hopital Necker - enfants malades
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- QUADRUPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 3 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-29
- Primary Completion
- 2024-09-30
- Completion
- 2024-09-30
Countries
- France
Study Locations
More Related Trials
-
Effect of Ev.FV on Wound Healing in Dystrophic Epidermolysis Bullosa
NCT07230223 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Evaluating Sirolimus to Treat Autoimmune Blistering Dermatosis Pemphigus
NCT01313923 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
Allogeneic ABCB5-positive Stem Cells for Treatment of Epidermolysis Bullosa
NCT03529877 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Topical Everolimus in Patients With Tuberous Sclerosis Complex
NCT02860494 ·Status: WITHDRAWN ·Phase: PHASE2/PHASE3
-
A Study to Learn About the Safety and Efficacy of the Drug Oleogel-S10 in Japanese Patients With Epidermolysis Bullosa
NCT06917690 ·Status: RECRUITING ·Phase: PHASE3
-
Pilot Study Evaluating the Efficiency and the Tolerance of the PDT in the Treatment of Epidermal Dysplasia for Patients Affected by Hereditary DEB
NCT02004600 ·Status: WITHDRAWN ·Phase: NA
-
Open-Label Extension Study to Evaluate the Safety of SD-101 Cream in Participants With Epidermolysis Bullosa
NCT02090283 ·Status: TERMINATED ·Phase: PHASE2
-
Recessive Dystrophic Epidermolysis Bullosa Screening for Possible Gene Transfer
NCT00533572 ·Status: TERMINATED
-
Treatment of Epidermolysis Bullosa Dystrophica by Polyphenon E (Epigallocatechin 3 Gallate)
NCT00951964 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Evaluate the Use of Palifermin to Treat Toxic Epidermal Necrolysis
NCT02037347 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Evaluation of D-Fi for the Treatment of Wounds Due to DEB
NCT06892639 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
ESSENCE Study: Efficacy and Safety of SD-101 Cream in Participants With Epidermolysis Bullosa
NCT02384460 ·Status: COMPLETED ·Phase: PHASE3
-
Characteristics of Patients With Recessive Dystrophic Epidermolysis Bullosa
NCT01019148 ·Status: RECRUITING
-
Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa
NCT00904163 ·Status: COMPLETED
-
Open Label Extension Study to Evaluate the Long-term Safety of Zorblisa (SD-101-6.0) in Patients With Epidermolysis Bullosa
NCT02670330 ·Status: TERMINATED ·Phase: PHASE3
-
A Study of FCX-007 for Recessive Dystrophic Epidermolysis Bullosa (RDEB)
NCT02810951 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Targeting Collagen VII Antibodies in Bullous Diseases Using Efgartigimod IV (VYVGART)
NCT07011589 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
Autologous Transplantation of Cultured Fibroblast on Amniotic Membrane in Patients With Epidermolysis Bullosa
NCT01908088 ·Status: COMPLETED ·Phase: PHASE1
-
Targeting Collagen VII Antibodies With IV IgG in Dystrophic Epidermolysis Bullosa
NCT06834035 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Diacerin for the Treatment of Epidermolysis Bullosa Simplex
NCT02470689 ·Status: UNKNOWN ·Phase: PHASE2
-
Allogeneic ABCB5-positive Dermal Mesenchymal Stromal Cells for Treatment of Epidermolysis Bullosa (Phase III)
NCT05838092 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Efficacy of Granulocyte Colony Stimulating Factor (GCSF) In Patients With Dystrophic Epidermolysis Bullosa
NCT01538862 ·Status: COMPLETED ·Phase: PHASE2
-
Study of PTW-002 in Patients With Dominant or Recessive Dystrophic Epidermolysis Bullosa Due to Mutation(s) in Exon 73 of the COL7A1 Gene
NCT05529134 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
A Pilot Study to Explore the Role of Gut Flora in Epidermolysis Bullosa
NCT04213703 ·Status: WITHDRAWN
-
Study of Inflammatory Mechanisms in Epidermolysis Bullosa Simplex- Dowling Meara
NCT01556308 ·Status: COMPLETED ·Phase: NA