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- Essai clinique NCT07756138
Filsuvez in Moderate-to-Severe Epidermolysis Bullosa Simplex (FILS-EBS)
5 août 2026 mis à jour par: Joyce Teng, Stanford University
A Pilot Trial to Evaluate the Efficacy and Safety of Filsuvez in the Treatment of Moderate-to-Severe Epidermolysis Bullosa Simplex
This pilot study will look at whether the topical Birch Triterpenes (Filsuvez) gel is safe and helpful for adults and children 6 months of age and older who have moderate to severe epidermolysis bullosa simplex (EBS).
The study will examine whether the gel can reduce the number of blisters, help wounds heal faster, and improve comfort by reducing pain and itching and making daily activities easier.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
10
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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California
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Palo Alto, California, États-Unis, 94304
- Stanford University School of Medicine
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Chercheur principal:
- Joyce M. C. Teng, MD PhD
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Sous-enquêteur:
- Chaw-Ning Lee, MD PHD
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
- Subject has a documented diagnosis and confirmed clinical history of EBS. The Investigator will determine subject eligibility based on historical phenotypic presentation of EBS symptoms along with genetic/diagnosis documentation in order to determine EBS severity.
The following skin conditions are required:
- A minimum area of ~3% BSA containing active blisters/erosions, and freshly ruptured blisters across 50% of the TLA (as assessed by the PI). Skin erosions, keratoderma, fissures and/or erythema may also be present.
- Subjects will be permitted to treat their feet to assess plantar blister surface area but blistering on the feet is not a requirement for study inclusion.
- TLA may not be infected (as assessed by PI) or have been treated with a topical antibiotic within 14 days.
If the subject is a woman of childbearing potential (WOCBP) (Need to verify current labeling on use during pregnancy)
- Has a negative urine pregnancy test at baseline.
- Agrees to use an approved effective form of birth control with failure rates <1% per year (e.g., implant, injectable, combined oral contraceptive, intrauterine contraceptive device, sexual abstinence, vasectomized partner) during participation in the study.
- Is not nursing.
- Subject's laboratory values (blood and urine) are within the range of normal or abnormal values are within normal levels for the disease and in the opinion of the PI the values are not clinically relevant for study participation.
- Subject is in good, general health and free of any known disease state or physical condition which, in the investigator's opinion, might interfere evaluation of the EBS lesions during study or which exposes the subject to an unacceptable risk by study participation.
- Over the duration of the study, the subject agrees to not use any other topical therapies and/or impregnated dressings within the TLAs (e.g., medicated cleansers, CBD oil, MediHoney, Silvadene cream 1%, topicals containing antimicrobials, keratin, and/or collagen, lipid-colloid or polymeric membrane dressings, and/or hydrogels).
- Subject and/or legally appointed and authorized representative must be able and willing to follow study procedures and instructions to maintain compliance throughout the study period.
- The subject, parent, or legally appointed and authorized representative must have read, understood and signed an Institutional Review Board/Ethics Committee (IRB/EC) approved Informed Consent and Assent Form if applicable.
Exclusion Criteria:
Subject's use of prior or concomitant medication or medical treatments/procedures:
- Any investigational drug or therapy within 30 days.
- Systemic steroidal therapy within 30 days.
- Topical steroidal therapy in TLA within 14 days (Note: inhaled and ophthalmic products containing steroids are allowed).
- Systemic antibiotic therapy within 7 days.
- Currently receiving chemotherapy or radiation.
- Surgery within the previous 2 weeks (except for minor surgery, cosmetic or dental procedures as determined by the investigator).
- Started to take chronic medications (NSAIDs, antihistamines, etc.) at least 30 days prior to starting study medication.
Subject's medical history includes:
- Cancer that is currently undergoing treatment.
- Current systemic or ongoing skin infection.
- HIV/AIDS.
- Non-EBS skin disease (e.g., psoriasis, atopic dermatitis, etc.), or condition (e.g., sunburn) that, in the opinion of the investigator, might put the subject at undue risk by study participation or interferes with the study medication application or the study assessments.
- An illness (e.g., neurological, cardiovascular, respiratory, hepatic, renal, or metabolic disease), condition, or situation that in the opinion of the principal investigator is likely to interfere with the subject's participation in or completion of the study.
- Factors present in the subject and/or his/her legal representative that could interfere with study compliance such as inability to attend scheduled study visits or to perform study protocol procedures.
- Subject is a member of the investigational team or his/her immediate family.
- Other unspecified reasons that, in the opinion of the Investigator, make the subject unsuitable for enrollment.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Filsuvez
All the participants will apply Filsuvez about 3% BSA for 3 months and a follow-up visit 2 months later.
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All the participants will apply Filsuvez about 3% BSA for 3 months.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Blister surface area reduction of the target treatment areas
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Clinical photography will be used to assess changes in disease severity within the TLA and recurrence of blistering by measuring blister surface area in the TLA over time.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in EBSdart scores
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
|
Epidermolysis Bullosa Simplex Disease Activity and Response Tool (EBSdart) grades blistering and erosions/ulcerations in all body regions and fissures and keratoderma on the palms and soles, including the area affected.
IGA regional subscores are recorded separately for the palms, soles, trunk, upper extremities, and lower extremities, using palm- and sole-specific criteria where applicable.
A score range from 0-99, where higher scores indicate severe condition.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Palmoplantar Blister Surface Area
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Clinical photography will be used to assess changes in disease severity within the Palmoplantar blister surface area and recurrence of blistering by measuring blister surface area in the Palmoplantar blister surface area over time.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in Pain Score in Target Lesional Areas
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Using the adult or pediatric Patient-Reported Outcomes Measurement Information System (PROMIS) Measure form, peak pain during IP application will be reported on a weekly basis.
Pain will be compared between baseline and at the end of treatment.
The appropriate PROMIS Pain Interference Short Form will be administered based on the participant's age: the Adult Pain Interference Short Form 8a, the Pediatric Pain (8yo+) Interference Short Form 8a, or the Parent Proxy Pain (6m-8yo) Interference Short Form 8a.
Each item is scored on a 5-point Likert scale (1-5), where higher scores indicate greater pain interference with daily activities (1 = Not at All; 5 = Very Much).
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in Itch Score in Target Lesional Area
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Using the adult or pediatric PROMIS Measure form (8 yo +), itch characteristics will be reported on a weekly basis to track trends in how itch impacts daily living in Birch triterpenes at baseline versus 3 mo post treatment.
The appropriate PROMIS Pain Interference Short Form will be administered based on the participant's age: the Adult Itch Interference Short Form 8a, the Pediatric Itch Interference Short Form 8a, or the Parent Proxy Itch (6m-8yo) Interference Short Form 8a.
Each item is scored on a 5-point Likert scale (1-5), where higher scores indicate greater pain interference with daily activities (1 = Never; 5 = Almost always).
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in Quality of Life
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Participant's quality of life metrics will be reported on a weekly basis to track trends at baseline versus 3 mo post Birch Triterpenes treatment.
The Quality of Life in Epidermolysis Bullosa (QOLEB) questionnaire is a disease-specific instrument consisting of 17 items.
Each item is scored on a 4-point scale (0-3), yielding a total score ranging from 0 to 51, with higher scores indicating poorer quality of life and greater disease burden.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in Modified Foot Function Index(mFFI)
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Participant's mFFI will be reported on a biweekly basis to track changes with Birch Triterpenes.
The Modified Foot Function Index (mFFI) consists of 27 items that assess foot pain, disability, and activity limitation.
Each item is rated on an 11-point numeric rating scale (0-10), where 0 indicates no pain/no difficulty/Not at all and 10 indicates the worst pain imaginable or greatest difficulty/all the time.
Total scores range from 0 to 270, with higher scores representing worse foot function and greater disability.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Safety: Incidence of treatment-emergent adverse events (TEAEs)
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Safety monitoring will include clinical chemistry tests, physical examinations (including assessment of TLA), and vital sign measurements.
These assessments along with AE reviews will identify potential TEAEs.
Safety monitoring will include clinical laboratory testing (blood and urine) and urine pregnancy testing (as appropriate) only at Visit 1/Screening and visit 4/EOS.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Change in Palmoplantar Blister Surface Area- EBSDart scores
Délai: From enrollment to the end of treatment at Week12 and Week20 (EOS).
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EBSdart grades blistering and erosions/ulcerations in all body regions and fissures and keratoderma on the palms and soles, including the area affected.
IGA regional subscores are recorded separately for the palms, soles, trunk, upper extremities, and lower extremities, using palm- and sole-specific criteria where applicable.
A score range from 0-99.
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From enrollment to the end of treatment at Week12 and Week20 (EOS).
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Joyce Teng, MD, PhD, FAAD, Stanford University
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 octobre 2026
Achèvement primaire (Estimé)
2 juillet 2027
Achèvement de l'étude (Estimé)
18 juin 2028
Dates d'inscription aux études
Première soumission
24 juillet 2026
Première soumission répondant aux critères de contrôle qualité
5 août 2026
Première publication (Réel)
10 août 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
10 août 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
5 août 2026
Dernière vérification
1 juin 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies génétiques, innées
- Maladies de la peau
- Anomalies congénitales
- Maladies de la peau, Génétique
- Anomalies cutanées
- Maladies de la peau, vésiculobulleuses
- Maladies et anomalies congénitales, héréditaires et néonatales
- Maladies de la peau et du tissu conjonctif
- Épidermolyse bulleuse
- Épidermolyse Bulleuse Simplex
Autres numéros d'identification d'étude
- IRB-87068
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
produit fabriqué et exporté des États-Unis.
Oui
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .