Extension Study to PTR-01-002 (A Study in Recessive Dystrophic Epidermolysis Bullosa (RDEB) Patients Previously Treated With PTR-01)

Inclusion Criteria:

   1. 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.

   2. Has satisfactorily completed participation in PTR-01-002.

   3. 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.

   4. Be willing and able to comply with this protocol.

Exclusion Criteria:

   1. Has known systemic hypersensitivity to any of the inactive ingredients in PTR-01.

   2. Has previously had an anaphylactic reaction to PTR-01.

   3. Is pregnant or nursing.

   4. 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).

   5. Is anticipated to receive new regimens of antibiotics or other anti-infectives during
   the trial.

   6. Has any other medical or personal condition that, in the opinion of the Investigator,
   may potentially compromise the safety or compliance of the