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

Inclusion Criteria:

• Patient is a male or female at least 4 years of age.

• Patient has a documented diagnosis of generalize intermediate (previously Kӧbner) tosevere (previously EBS-DM) autosomal dominant epidermolysis bullosa simplex (EBS)and/or genetic mutation in either the K14 or K5 genes consistent with generalizedintermediate to severe EBS. The Investigator will determine patient eligibilitybased on historical phenotypic presentation of EBS symptoms along withgenetic/diagnosis documentation in order to determine EBS severity. (If generalizedintermediate 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 kneeand top of the thigh) or 2) torso (excluding the groin and apocrine areas). Thefollowing 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 rupturedblisters across 50% of the TLA (as assessed by the principal investigator (PI)). Skin erosions, keratoderma, fissures and/or erythema may also bepresent.

• Patients will be permitted to treat their feet to assess plantar blistersurface area but blistering on the feet is not a requirement for studyinclusion.

• TLA may not be infected (as assessed by PI) or have been treated with a topicalantibiotic 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 orabnormal values are within normal levels for the disease and in the opinion of thePI the values are not clinically relevant for study participation.

• Patient is in good, general health and free of any known disease state or physicalcondition which, in the investigator's opinion, might impair evaluation of the EBSlesions 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 topicaltherapies 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 andwilling to follow study procedures and instructions in order to maintain compliancethroughout 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 productscontaining 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 ordental procedures as determined by the investigator).

• Started to take chronic medications (NSAIDs, antihistamines, etc.) at least 30days 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 withthe study medication application or the study assessments.

• An illness (e.g., neurological, cardiovascular, respiratory, hepatic, renal, ormetabolic disease), condition, or situation that in the opinion of theprincipal investigator is likely to interfere with the patient's participationin or completion of the study.

• Factors present in the patient and/or his/her legal representative that couldinterfere with study compliance such as inability to attend scheduled study visitsor 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 patientunsuitable for enrollment.