A Phase II, Placebo Controlled, Clinical Trial of Topical TolaSure Targeting Aggregated Mutant Keratin in Epidermolysis Bullosa Simplex

NCT ID: NCT07027345

Last Updated: 2025-09-11

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-30
• Study Completion Date: 2026-09-30

Brief Summary

This Phase II clinical study will assess the efficacy, safety and tolerability of topical TolaSure Gel in adults and pediatric patients (4 years of age and older) diagnosed with generalized intermediate to severe epidermolysis bullosa simplex (EBS). Each patient (40 to complete) will be enrolled in the study and will be randomized to receive either TolaSure Gel or a topical Placebo for daily application for 2-months. After 2-months, all patients will receive TolaSure Gel to daily apply for an additional 2-months. A remote follow-up visit will occur 2-months after the end of study. Total time in the study is 6-months. Patients will be applying study medication to randomized treatment area(s) (a minimum of ~2-3% Body Surface Area (BSA)), with the option to treat their feet as well throughout the study.

Detailed Description

This is a closed-label, Phase II clinical study to assess the efficacy, safety and tolerability of the investigational product (IP), topical TolaSure Gel, 5% w/w, in adults and pediatric patients diagnosed with generalized intermediate to severe epidermolysis bullosa simplex (EBS). TolaSure Gel, 5% w/w and Placebo tubes will be placed into kits where all labels (tubes and kit labels) will be blinded for drug content. Kits will be bundled (based on expected amount of study gel usage) and distributed randomly to patients [Goal of patient population, 1:1 M:F and approximately 70% pediatric patients].

Each patient (40 to complete) will be enrolled in the study and once a blistering flare is confirmed by the clinical study team, and the patient will be randomized to receive either TolaSure Gel, 5% w/w or Placebo (50:50 chance).

For Part 1 of the study, daily application of randomized treatment for 2 months will be applied to selected Target Lesional Areas (TLAs; a minimum area of approximately 2-3% Body Surface Area (BSA)). If a TLA resolves completely the patient will continue to treat designated area(s). Additionally, patients have the option to daily treat their feet.

For Part 2 of the study, a single arm crossover will then allow those patients that received Placebo to go on TolaSure Gel, 5% w/w for a subsequent 2 months. The patients already in the TolaSure Gel, 5% w/w cohort will continue with daily IP application for an additional 2 months as well. Again, patients have the option to continue to treat their feet. At Part 2 End of Study (EOS), patients will cease IP application and EOS procedures will be completed. Patients can have optional perilesional biopsies taken from a treated and untreated area to evaluate changes in ultrastructural pathology. A patient follow-up visit will occur after 6 months (2-months after last treatment application).

The primary endpoint will assess changes in disease severity within the TLAs and recurrence of blistering using clinical imaging to assess blister surface area over time. The secondary efficacy endpoints will evaluate blistering on the feet, subject self-assessments including pain, itch, modified Foot Function Index (mFFI), and Quality of Life (QoL) assessment.

Safety endpoints will include the incidence of treatment-emergent adverse events (TEAEs). In order to provide adequate assurance of subject safety, safety monitoring will include physical exams, vital sign measurements, clinical laboratory testing (blood and urinalysis), and urine pregnancy testing (as appropriate). These safety assessments in addition to adverse event (AE) reviews will be sufficient to identify potential TEAEs.

The information obtained from these assessments will be utilized to examine the efficacy of TolaSure treatment in ameliorating EBS symptoms as well as the accuracy of the proposed mechanism of action (MOA) of TolaSure for this disease indication.

Conditions

Epidermolysis Bullosa Simplex

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

5% TolaSure Topical Gel

5% (w/w) TolaSure Gel

Group Type: ACTIVE_COMPARATOR

5% TolaSure Topical Gel

Intervention Type: DRUG

TolaSure Topical Gel is applied once-daily to designated treatment areas for up to 4 months (Part 2 End of Study).

Topical Placebo Gel

Placebo Control Gel

Group Type: PLACEBO_COMPARATOR

Topical Placebo Gel

Intervention Type: DRUG

Topical Placebo Gel is applied once-daily to designated treatment areas for up to 2 months (Part 1 End of Study).

Interventions

5% TolaSure Topical Gel

TolaSure Topical Gel is applied once-daily to designated treatment areas for up to 4 months (Part 2 End of Study).

Intervention Type: DRUG

Topical Placebo Gel

Topical Placebo Gel is applied once-daily to designated treatment areas for up to 2 months (Part 1 End of Study).

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patient is a male or female at least 4 years of age.
• Patient has a documented diagnosis of generalize intermediate (previously Kӧbner) to severe (previously EBS-DM) autosomal dominant epidermolysis bullosa simplex (EBS) and/or genetic mutation in either the K14 or K5 genes consistent with generalized intermediate to severe EBS. The Investigator will determine patient eligibility based on historical phenotypic presentation of EBS symptoms along with genetic/diagnosis documentation in order to determine EBS severity. (If generalized intermediate to severe EBS is suspected but not diagnosed or genetically confirmed, confirmatory testing will be performed).
• Patient is actively flaring in one of the preferred target lesional areas (TLAs): 1) lower extremities (ideally below the knee and above the ankle or between the knee and top of the thigh) or 2) torso (excluding the groin and apocrine areas). The following skin conditions are required for treatment purposes:

• A flare is defined as a minimum area of ~2-3% Body Surface Area (BSA) containing intact blisters (of varying size and number), and freshly ruptured blisters across 50% of the TLA (as assessed by the principal investigator (PI)). Skin erosions, keratoderma, fissures and/or erythema may also be present.
• Patients 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 patient is a woman of childbearing potential (WOCBP),

• Has a negative urine pregnancy test.
• 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 (and at least 3 months thereafter).
• Is not nursing.
• Patient'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.
• Patient is in good, general health and free of any known disease state or physical condition which, in the investigator's opinion, might impair evaluation of the EBS lesions or which exposes the subject to an unacceptable risk by study participation.
• Over the duration of the study, the patient agrees to not use any other topical therapies and/or impregnated dressings within the TLAs (e.g., medicated cleansers, CBD oil, MediHoney, Silvadine cream 1%, topicals containing antimicrobials, keratin, and/or collagen, lipido-colloid or polymeric membrane dressings, and/or hydrogels).
• Patient and/or legally appointed and authorized representative must be able and willing to follow study procedures and instructions in order to maintain compliance throughout the study period.
• The patient or legally appointed and authorized representative must have read, understood and signed an Institutional Review Board/Ethics Committee (IRB/EC) approved Informed Consent or Assent Form.

Exclusion Criteria

• Patient'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 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.
• Patient's medical history includes:

• Cancer that is currently undergoing treatment.
• History of chronic and severe vitamin, mineral, or protein deficiency.
• Current systemic infection.
• HIV/AIDS.
• Non-EBS skin disease (e.g., psoriasis, atopic dermatitis, eczema, sun damage, etc.), or condition (e.g., sunburn) that, in the opinion of the investigator, might put the patient 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 patient's participation in or completion of the study.
• Factors present in the patient 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.
• Patient is a member of the investigational team or his/her immediate family.
• Other unspecified reasons that, in the opinion of the Investigator, make the patient unsuitable for enrollment.

• Minimum Eligible Age: 4 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Northwestern University Feinberg School of Medicine

OTHER

Sponsor Role: collaborator

Ann & Robert H Lurie Children's Hospital of Chicago

OTHER

Sponsor Role: collaborator

Stanford University

OTHER

Sponsor Role: collaborator

Lucile Packard Children's Hospital

OTHER

Sponsor Role: collaborator

BioMendics, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Stanford University School of Medicine, Dermatology Department

Palo Alto, California, United States

Site Status: RECRUITING

NU Dermatolgy CTU

Chicago, Illinois, United States

Site Status: RECRUITING

Countries

United States

Facility Contacts

Thomas Buschbacher

Role: primary

tbusch@stanford.edu

650-313-0354

NU Dermatolgy CTU

Role: primary

NUderm-research@northwestern.edu

312-227-6817

Related Links

https://www.biomendics.com

BioMendics, LLC

https://med.stanford.edu/dermatology/research/research_1/currentstudies.html

Stanford Medicine, Dermatology, Current EB Studies

https://www.feinberg.northwestern.edu/sites/dermatology/research/clinical-trials.html

Northwestern Medicine, Department of Dermatology Clinical Trials

Other Identifiers

TAMES-02

Identifier Type: -

Identifier Source: org_study_id