A Study to Evaluate the Efficacy of ELAPR in Women With Striae Distensae Alba

NCT ID: NCT02510768

Last Updated: 2018-07-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-04-16
• Study Completion Date: 2018-03-06

Brief Summary

The study is designed to evaluate the efficacy of two formulations of a cross-linked tropoelastin matrix given the product codes ELAPR002f and ELAPR002g (collectively referred to as ELAPR or ELAPR002) for the treatment of Striae Distensae (SD) alba when administered as intradermal implants.

Detailed Description

The study will consist of six study visits. There will be a screening visit to confirm eligibility and to assess baseline parameters (Day -28 to Day -1). For enrolled subjects there will be three intradermal (i.d.) treatment sessions of ELAPR002f or ELAPR002g and placebo, given at one-monthly intervals (approximately Day 0, Day 28 and Day 56). There will be a safety assessment visit 7 days after the first treatment session (Day 7) to review any adverse events and assess the implant sites. ELAPR002f or ELAPR002g will be administered alone vs. placebo. Subjects will be followed for a total of 12 weeks (to Day 84) following the first treatment, with efficacy and safety assessments undertaken at each study visit. At the final follow-up visit (Day 84) a biopsy sample will be taken from each of the treated SDs (active and placebo treated), together with a control biopsy of normal skin collected from an area of the lateral aspect of the abdomen, hip or thigh without an SD alba. Each study subject will act as their own control with active and placebo treatments given single-blind to contralateral sides of the abdomen, hip or thigh, into matched and paired SD. Prior to administration the selected injection sites along the length of SD alba to be treated will be identified and marked with a semi-permanent mark to ensure consistency of anatomic sites for treatment and biopsy. Follow-up period extended to D168, D336 and D504.

Conditions

Striae Distensae

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

ELAPR002f

ELAPR002f A tropoelastin polymer cross-linked with hyaluronic acid.

Group Type: EXPERIMENTAL

ELAPR002f

Intervention Type: DEVICE

Intradermal implant

ELAPR002g

ELAPR002g A tropoelastin polymer cross-linked with hyaluronic acid.

Group Type: EXPERIMENTAL

ELAPR002g

Intervention Type: DEVICE

Intradermal implant

Saline

Saline

Group Type: PLACEBO_COMPARATOR

Saline

Intervention Type: DEVICE

Intradermal implant

Interventions

ELAPR002f

Intradermal implant

Intervention Type: DEVICE

ELAPR002g

Intradermal implant

Intervention Type: DEVICE

Saline

Intradermal implant

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Female subjects with at least four abdominal, hip or thigh SD alba which are approximately bilaterally symmetrical (similar dimensions/location/colour) and are of at least 6 cm in length and no more than 5mm wide.
• SD alba within an area of skin of otherwise normal, smooth, mainly flat appearance.
• Age: 30 - 55 years.
• BMI: 18.5 to 35.0 Kg/m2.
• Capable of providing voluntary informed consent.
• Good general health.
• Female subjects who are sexually active will be of non-child bearing potential (i.e., surgically sterilized or postmenopausal), abstain from sexual intercourse, or use a reliable method of contraception (e.g. hormonal contraceptive, condom, IUD) for at least 30 days prior to dosing and during the duration of the study.
• Fitzpatrick skin types II, III or IV.

Exclusion Criteria

• SD alba within an area of otherwise abnormal skin appearance including unusual lumpiness or abnormal skin laxity.
• Current or previous medical or surgical treatment of SD.
• Known hypersensitivity to tropoelastin, hyaluronic acid or any other component of ELAPR002f or ELAPR002g.
• Female subjects with a positive pregnancy test, women refusing to agree to adequate contraception and pregnancy tests during the study, or women who are planning to become pregnant during the period of the trial.
• Participation in a clinical trial of a pharmacological agent within 1 month prior to screening.
• Clinically significant haematology or biochemistry findings at screening.
• Positive test for hepatitis B, hepatitis C or HIV at screening.
• Bleeding diathesis, anticoagulant drugs, thrombocytopenia or clinically significant prolonged activated partial thromboplastin time (APTT) or prothrombin time (PT).
• Chronic use of aspirin, other non-steroidal anti-inflammatory drugs or other anti-platelet agents.
• History of keloid formation.
• Systemic corticosteroids within last 12 weeks.
• Diabetes or other metabolic disorders that may interfere with the subject's response to treatment in the opinion of the investigator.
• Any serious medical condition which in the opinion of the investigator would have a strong possibility of requiring systemic corticosteroid medication.
• Females who are pregnant or lactating.
• Previous administration of tropoelastin.
• A history of anaphylaxis or allergic reactions including any known hypersensitivity to lidocaine.
• Use of any investigational product on the intended implant site in the previous 12 months.
• Fitzpatrick skin types I, V or VI.
• Any other factor that in the opinion of the Investigator would make the subject unsafe or unsuitable for the study.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Elastagen Pty Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hammersmith Medicines Research

London, , United Kingdom

Countries

United Kingdom

Other Identifiers

ELAPR-P1C

Identifier Type: -

Identifier Source: org_study_id