Extension Study to PTR-01-002 (A Study in Recessive Dystrophic Epidermolysis Bullosa (RDEB) Patients Previously Treated With PTR-01)
- Registration Number
- NCT05143190
- Lead Sponsor
- Phoenix Tissue Repair, Inc.
- Brief Summary
A sub-set of patients who participated in PTR-01-002 will be enrolled in an open-label study, if they meet the study eligibility criteria.
- Detailed Description
Protocol PTR-01-003 is a 4-part Phase 2, open-label study of PTR-01 in patients who satisfactorily completed study PTR-01-002 and meet current enrollment criteria.
In Part 1, patients will be monitored monthly for up to 2 months with patient-reported and Investigator assessments. In Part 2, patients will receive a dose of 3.0 mg/kg every week for a total of 4 doses. This will be followed by Part 3 in which patients will receive a dose of 3.0 mg/kg monthly for a total of 5 additional doses. At the end of each dosing period, efficacy assessments will be performed. During Part 4, patients will be evaluated at Months 1 and 3 after completion of dosing to assess the durability of wound healing and other efficacy parameters. Safety will be assessed continuously throughout the study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 2
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Willing to provide informed consent form, or if 12 to <18 years of age, legal guardian has provided informed consent form and the minor has signed an assent form acknowledging that they understand and agree to study procedures.
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Has satisfactorily completed participation in PTR-01-002.
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Agrees to use contraception as follows:
- For women of childbearing potential (WOCBP) agrees to use highly effective contraceptive (including abstinence) methods from Screening, through the study, and for at least 10 weeks after the last dose of study drug. Non-childbearing potential is defined as a female who meets either of the following criteria: age ≥50 years and no menses for at least 1 year or documented hysterectomy, bilateral tubal ligation, or bilateral oophorectomy.
- For males, agrees to use a condom with any WOCBP sexual partner from Day 1 of study treatment, through the study, and at least 10 weeks after the last dose of study drug.
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Be willing and able to comply with this protocol.
- Has known systemic hypersensitivity to any of the inactive ingredients in PTR-01.
- Has previously had an anaphylactic reaction to PTR-01.
- Is pregnant or nursing.
- Has received in the last six months any investigational gene therapy product or in the last three months any non-gene therapy investigational products (other than PTR-01).
- Is anticipated to receive new regimens of antibiotics or other anti-infectives during the trial.
- Has any other medical or personal condition that, in the opinion of the Investigator, may potentially compromise the safety or compliance of the
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description PTR-01 PTR-01 All patients will receive a PTR-01 dose of 3.0 mg/kg once weekly every week for a total of 4 doses, followed by a dose of 3.0 mg/kg once monthly for a total of 5 doses.
- Primary Outcome Measures
Name Time Method Sustained wound healing Up to 246 days Change in a majority of target lesions of at least 2 levels using a 7-point (1-7) Global Impression of Change instrument (7 being the worst)
Incidence of treatment-emergent adverse events Up to 246 days Safety and tolerability, as assessed by treatment-emergent adverse events
- Secondary Outcome Measures
Name Time Method Change in wound surface area Up to 246 days Wound surface area of lesions as assessed by medical photography using the Canfield RUBI 3D imaging system
Delivery of recombinant collagen 7 (PTR-01) to skin Up to 246 days Amount of recombinant collagen 7 (PTR-01) incorporation to skin as compared to normal human skin assessed by immunofluorescence using NC1 \& NC2 antibody staining
Formation of anchoring fibrils Up to 246 days Formation of new anchoring fibrils as measured by electron microscopy
Change in skin integrity, as assessed by suction blister time Up to 246 days Change in skin integrity, as assessed by suction blister time
Change in skin integrity, as assessed by time to re-blistering Up to 246 days Change in skin integrity, as assessed by time to re-blistering
Change in the impact of itch on quality of life Up to 246 days Change in the impact of itch on quality of life, as assessed by the Pruritus-Specific Quality of Life Instrument (ItchyQoL), maximum score of 110 (worst)
Stabilization of corneal symptoms Up to 246 days Stabilization of corneal symptoms (eye symptoms), as assessed by the Epidermolysis Bullosa Eye Disease Index (EB-EDI), maximum score of 100 (worst)
Change in itch severity, as assessed by modified Patient-Reported Outcome Measurement Information System (PROMIS) itch domains Up to 246 days Severity of itch, as assessed by modified Patient-Reported Outcome Measurement Information System (PROMIS) itch domains, maximum score of 5 (worst)
Change in pain severity, as assessed by modified Patient-Reported Outcome Measurement Information System (PROMIS) pain domains Up to 246 days Change in pain severity, as assessed by Patient-Reported Outcome Measurement Information System (PROMIS) pain domains, maximum score of 5 (worst)
Rate of change in nutritional markers (hematocrit) Up to 246 days Change of nutritional markers, as assessed by hematocrit
Change in pain severity, as assessed by the Instrument for Scoring Clinical Outcomes for Research of Epidermolysis Bullosa (iscorEB) Up to 246 days Change in pain severity, as assessed by the Instrument for Scoring Clinical, maximum score of 234 (worst)
Change of dysphagia, as assessed using the Brief Esophageal Dysphagia Questionnaire Up to 246 days Change of dysphagia, as assessed using the Brief Esophageal Dysphagia Questionnaire, maximum score is 40 (worst)
Stabilization of dysphagia, as assessed using the Brief Esophageal Dysphagia Instrument Up to 246 days Stabilization of dysphagia, as assessed using the Brief Esophageal Dysphagia Instrument, maximum score of 40 (worst)
Rate of change in nutritional markers (hemoglobin) Up to 246 days Change of nutritional markers, as assessed by hemoglobin
Rate of change in nutritional markers (total protein/albumin) Up to 246 days Change of nutritional markers, as assessed by total protein/albumin
Rate of change in nutritional markers (Fe/TIBC) Up to 246 days Change of nutritional markers, as assessed by total Fe/TIBC
Rate of change in nutritional markers (C-reactive protein) Up to 246 days Change of nutritional markers, as assessed by total C-reactive protein
Change in corneal symptoms Up to 246 days Change of corneal symptoms (eye symptoms), as assessed by the Epidermolysis Bullosa Eye Disease Index (EB-EDI), maximum score of 100 (worst)
Change in Investigator Global Impressions of Change (IGIC) Up to 246 days Global impressions of change, as assessed through IGIC (1-7), 7 being worst
Change in Investigator Patient Impressions of Change (PGIC) Up to 246 days Global impressions of change, as assessed through PGIC (1-7), 7 being worst
Change in overall quality of life, as assessed by the Quality of Life in Epidermolysis Bullosa (QOLEB) questionnaire Up to 246 days Change in overall quality of life, as assessed by the Quality of Life in Epidermolysis Bullosa (QOLEB) questionnaire maximum score is 67 (worst)
Change in amount of wound care Up to 246 days Change in amount of wound care, as assessed by patient interviews
Change in overall health Up to 246 days Change in overall disability, as assessed by the Health Assessment Questionnaire or Children's Health Assessment Questionnaire (HAQ/CHAQ) maximum score is 3 (worst)
Change in mental health Up to 246 days Change in mental health, as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) mental health domains, maximum score is 5 (worst)
Change in social function Up to 246 days Change in social functioning, as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) social function domains, maximum score is 4 (worst)
Change in time for wound care Up to 246 days Change in time for wound care, as assessed by patient interviews
Change in cost of wound care Up to 246 days Change in cost of wound care, as assessed by patient interviews
Change in overall patient impression of quality of life Up to 246 days Change in overall anecdotal quality of life, as assessed by one-on-one patient interviews
Change in overall patient impression of disability Up to 246 days Change in overall anecdotal disability, as assessed by one-on-one patient interviews
Effect of anti-drug antibodies (ADA) on pharmacokinetics parameter of clearance of PTR-01 Up to 246 days Correlate ADA with clearance of PTR-01
Effect of anti-drug antibodies (ADA) on pharmacokinetics parameter of PTR-01 half-life Up to 246 days Correlate ADA with PTR-01 half-life
Effect of anti-drug antibodies (ADA) on pharmacokinetics parameter Cmax Up to 246 days Correlate ADA with Cmax
Effect of anti-drug antibodies (ADA) on pharmacokinetics parameter Tmax Up to 246 days Correlate ADA with Tmax
Effect of anti-drug antibodies (ADA) on pharmacokinetics parameter Area Under the Curve (AUC) Up to 246 days Correlate ADA with Area Under the Curve (AUC)
Trial Locations
- Locations (2)
Columbia University Irving Medical Center
🇺🇸New York, New York, United States
Stanford University
🇺🇸Redwood City, California, United States