A Double-blind, Intra-individual Comparison, POC Trial of AC-203 in EB Patients

NCT03468322 | Completed Phase 2

• 1 other identifier: AC-203-EBS-005
• Study Type: interventional
• Target: 9
• Locations: 1 country
• Sites: 2

Brief Summary

Inherited epidermolysis bullosa (EB) is a genetic skin disorder characterized by skin fragility and recurrent blister formation. More and more evidence has suggested that the skin lesions initially caused by genetic mutations may be further aggravated by inflammatory responses. Several reports showed successful alleviation of EB symptoms upon treatment with immunomodulatory therapies. Modulation of proinflammatory cytokine IL-1β has shown promising results in alleviating epidermolysis bullosa simplex (EBS), a major subtype of inherited EB, by downregulating IL-1β-mediated JNK/MAPK signaling pathway. This data further supports the potential of using cytokine modulators to treat EB. AC-203, a topical formulation, can inhibit the production and activity of IL-1β, down-regulate IL-1β receptors, and increase IL1β-receptor antagonist (IL1-Ra) expression. In addition, AC-203 has been reported to inhibit anti-BP180 autoantibody-induced IL-6/IL-8 upregulation in cultured keratinocytes and LPS-induced IL-6 upregulation in cultured macrophages. Furthermore, AC-203 was also found to inhibit the formation of NLRP3 inflammasome, which plays essential roles in induction of caspase-1-dependent pyroptosis and release of inflammatory cytokines IL-1β and IL-18. These studies demonstrated the cytokine modulatory properties of AC-203 and pointed out the possible application of AC-203 in a variety of inflammatory diseases. This study is designed to test the efficacy, safety, tolerability, and pharmacokinetics of AC-203 ointment (vs. placebo) in patients with inherited EB.

Conditions

Inherited Epidermolysis Bullosa

Outcome Measures

Primary Outcomes (1)

• Percentage change in lesion surface area from baseline by treatment

  2, 4, 5, 6, 8, 12 Weeks

Secondary Outcomes (6)

• Percentage change in blister number from baseline by treatment

  2, 4, 5, 6, 8, 12 Weeks

• Proportion of subjects with at least 40% reduction in blister number from baseline by treatment

  2, 4, 5, 6, 8, 12 Weeks

• Pruritus assessment scale changes from baseline by treatment

  2, 4, 5, 6, 8, 12 Week

• Pain assessment scale changes from baseline by treatment

  2, 4, 5, 6, 8, 12 Weeks

• IL-1beta concentrations and changes from baseline

  8 Weeks

Study Arms (2)

AC-203 1% ointment

EXPERIMENTAL

AC-203 1% ointment, QD

Drug: AC-203

Vehicle ointment

PLACEBO COMPARATOR

Vehicle ointment, QD

Drug: Vehicle

Interventions

AC-203 DRUG

The investigational product is formulated as 1% topical ointment

AC-203 1% ointment

Vehicle DRUG

Vehicle-only control study medication is the same formulation as investigational product without active ingredient

Vehicle ointment

Eligibility Criteria

• Age: 2 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Subject is at least 2 years of age.
• Subject has a clinical diagnosis of EB.
• Subject has a laboratory confirmed diagnosis of inherited EB based on electron microscopy and/or immunofluorescence antigenic mapping.
• Subject has two comparable areas with 1% - 5% BSA each. These two areas could be on any body surface except the face, scalp, groin, palms and soles. Percentage BSA of the designated areas within subject should be the same. Comparable areas are defined as having similar lesion (i.e., blisters, erosions, erythema and crusts) history and current lesion status by investigator's judgement on each area at Screening Visit (Visit 1) and Day 1 (Visit 2).
• Is male, or is female and meets all the following criteria:
• Not breastfeeding
• If of childbearing potential (defined as non-post-hysterectomy or non-post-menopausal \[≥50 years of age and amenorrheic for at least 1 year\]), must have a negative pregnancy test result at Visit 1, and must practice and be willing to continue to practice appropriate birth control during the entire duration of the study.
• Is able to read, understand, and sign the Informed Consent Form (ICF), answer the study questionnaires, communicate with the investigator, and understand and comply with protocol requirements, OR Informed consent received from subject's parents/caregiver or legal guardian (when subject \< 20 years).

You may not qualify if:

• Subject has a current malignancy, or a history of treatment for a malignancy within two years.
• Systemic infections.
• Subjects who are pregnant, lactating, or planning a pregnancy during the study.
• History of allergy or hypersensitivity to any component of study medication.
• Any other significant diseases, conditions, or laboratory values which, in the opinion of the investigator, might make participation not in the subject's best interest or confound the interpretation of study results.
• Any prior use of approved or investigational biologic anti-inflammatory therapy within 6 months prior to screening, including but not limited to: anakinra, rilonacept, canakinumab, etanercept, adalimumab, infliximab, rituximab, certolizumab, golimumab, tocilizumab, bertilimumab, or abatacept.
• Use of non-steroid immunosuppressants including but not limited to azathioprine, mycophenolate, cyclophosphamide, chlorambucil, methotrexate, tacrolimus, or cyclosporine in the 2 weeks prior to screening.
• Has been treated with gentamicin within 90 days prior to screening (Note: products containing gentamicin used on eyes are allowed).
• Has been treated with minocycline, oxytetracycline, tetracycline or doxycycline within 7 days prior to screening.
• Subjects has used any topical allantoin ≥ 3% within 30 days prior to screening.
• Has been treated systemic steroid within 30 days prior to screening.
• Prior treatment with any investigational therapy within 30 days prior to screening.
• Is an immediate family member (spouse, parent, child, or sibling; biological or legally adopted) of personnel directly affiliated with the study at the clinical study site, or is directly affiliated with the study at the clinical study site.
• Is employed by sponsor (i.e., is an employee, temporary contract worker, or designee responsible for the conduct of the study).

Sponsors & Collaborators

• TWi Biotechnology, Inc.: lead

Study Sites (2)

Mackay Memorial Hospital

Hsinchu, Taiwan

Location

National Cheng Kung University Hospital

Tainan, Taiwan

Location

MeSH Terms

Interventions

diacerein

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Intra-individual comparison

Study Record Dates

• First Submitted: March 8, 2018
• First Posted: March 16, 2018
• Study Start: October 20, 2018
• Primary Completion: April 9, 2019
• Study Completion: April 9, 2019
• Last Updated: April 16, 2019

Record last verified: 2019-04

Locations

TW (2)