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Phase 4 Master Protocol for Patients Prescribed Prademagene Zamikeracel for the Treatment of Wounds

4. august 2026 oppdatert av: Abeona Therapeutics, Inc

The Master Protocol includes 3 studies (Study A, Study B, and Study C) that will evaluate pz-cel and related processes in the post-marketing setting.

Study A investigates the efficacy and safety of non-conforming pz-cel in patients with Recessive Dystrophic Epidermolysis Bullosa (RDEB).

Study B enables the collection of additional biopsy samples from patients receiving treatment with pz-cel.

Study C assesses the efficacy and safety of pz-cel in patient populations not represented in the VIITAL clinical trial (NCT04227106).

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

The Master Protocol includes 3 studies (Study A, Study B, and Study C) that will evaluate pz-cel (LZRSE-COL7A1 gene-corrected cellular sheets with type VII collagen [C7] expression) and related processes in the post-marketing setting.

Pz-cel is a genetically engineered autologous cell therapy indicated for the treatment of wounds associated with RDEB. Pz-cel is composed of autologous keratinocytes from patients with mutations in the collagen type VII alpha 1 chain (COL7A1) gene, which have been transduced ex vivo with the Moloney leukemia virus-derived retroviral vector (LZRSE)-COL7A1. The gene-corrected cellular sheets express functional C7.

The pz-cel sheets are a one-time surgical application to debrided and cauterized wound beds of the corresponding patients with DEB. The COL7A1 transgene integrates into the host cell genome, resulting in durable expression and secretion of collagen protein, which addresses the underlying mechanism of the disease.

Study A is an open-label, non-randomized study in patients who are expected to receive gene-corrected cellular sheets (pz-cel) for the treatment of RDEB wound sites in the post-marketing setting and whose manufactured patient-specific batch of pz-cel intended for commercial treatment did not meet commercial release criteria, but had no safety concerns associated with its use. This study will allow surgical application of such non-conforming pz-cel when the benefit of application outweighs the risks. All patients will be followed through 24 weeks after treatment and may be eligible for further follow-up after Week 24. Patients will be evaluated at their Screening visit (30 days before surgery), at Day 0 (Surgery day), by phone on Week 4 (Month 1) and by Telehealth or Clinic Visit at Week 12 (Month 3) and Week 24 (Month 6).

Study B is a study to collect additional biopsy samples from patients who are expected to receive treatment with pz-cel in the post-marketing setting. The additional biopsy samples are being collected to support pz-cel product optimization. Patients receiving treatment with pz-cel can consent to have 2 additional 8-mm biopsies for use in the pz-cel assay and process development as well as in the optimization of the pz-cel manufacturing processes. The study will consist of Screening (in-person or via phone and eConsent), a pre-surgery biopsy and an End of Study Phone call 10-14 days after biopsy.

Study C is an open-label, non-randomized study in patients who are prescribed gene-corrected cellular sheets (pz-cel) in the post-marketing setting and who are part of a patient population not represented in the VIITAL Clinical Trial (NCT04227106). This study will enable patients with wounds that could benefit from treatment with pz-cel, especially those requiring special access for application of pz-cel, to receive pz-cel. All patients will be followed through 24 weeks after treatment and may be eligible for further follow-up after Week 24. Patients will be evaluated at their Screening visit (25-60 days before surgery), at Day -1 (one day prior to surgery), at Day 0 (Surgery Day), by phone on Week 4 (Month 1) and by Telehealth or Clinic Visit at Week 12 (Month 3) and Week 24 (Month 6).

Studietype

Intervensjonell

Registrering (Antatt)

100

Fase

  • Fase 4

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Study A

Inclusion Criteria

  1. Willing and able to provide informed consent/assent; if under the age of 18, guardian(s) is (are) willing and able to provide consent.
  2. Patients who are expected to receive pz-cel manufactured as intended for commercial treatment; however, the final manufactured product was non-conforming and therefore did not meet commercial release criteria.
  3. All women of childbearing potential should discuss reproductive and breastfeeding plans and precautions with the treating physician in accordance with the considerations for special populations in the United States Prescribing Information (USPI).

Exclusion Criteria

  1. Inability to adequately follow the protocol and ensure the protection of cellular sheet sites, as determined by the Investigator.
  2. Hypersensitivity to vancomycin or amikacin.
  3. The presence of medical illness expected to complicate participation and/or compromise the safety of this technique, such as, but not limited to, active infection with human immunodeficiency virus (HIV), hepatitis B, or hepatitis C.
  4. Evidence of systemic infection.
  5. Current evidence of squamous cell carcinoma (SCC) in the area that will undergo pz-cel application.
  6. Grade 3 clinical event or laboratory abnormality prior to pz-cel treatment, with the exception of abnormalities such as esophageal strictures, anemia, low albumin, and pain/itch, which are expected in patients with severe DEB.
  7. Any other circumstance where the Investigator believes that it is not appropriate for the patient to participate in the study.

Study B

Inclusion Criteria

  1. Willing and able to provide informed consent/assent; if under the age of 18, guardian(s) is (are) willing and able to provide consent.
  2. Patients who are expected to receive treatment with pz-cel and are receiving a biopsy prior to pz-cel application in the post-marketing setting.

Exclusion Criteria

1. Any circumstance where the Investigator believes that the patient may not be appropriate for participation in the study.

Study C

Inclusion Criteria:

  1. Willing and able to provide informed consent/assent; if under the age of 18, guardian(s) is (are) willing and able to provide consent.
  2. Patients who were prescribed pz-cel for commercial treatment but require special access defined in the protocol for treatment to occur.
  3. All women of childbearing potential must have a negative urine pregnancy test and agree to use a reliable birth control method throughout the duration of the study.

Exclusion Criteria:

  1. Inability to properly follow protocol assessments and protect cellular sheet sites as determined by the Investigator.
  2. Currently enrolled in an interventional clinical trial involving an investigational medicinal product to treat DEB or receipt of the investigational therapy within the 3 months prior to pz-cel application.
  3. Breastfeeding.
  4. The presence of medical illness expected to complicate participation and/or compromise the safety of this technique, such as, but not limited to, active infection with human immunodeficiency virus (HIV), hepatitis B, or hepatitis C.
  5. Evidence of systemic infection.
  6. Current evidence or a history of SCC in the area that will undergo pz-cel application.
  7. Active drug or alcohol addiction.
  8. Hypersensitivity to vancomycin or amikacin.
  9. Grade 3 clinical event or laboratory abnormality prior to pz-cel treatment, with the exception of abnormalities such as esophageal strictures, anemia, low albumin, and pain/itch, which are expected in patients with severe DEB.
  10. Any other circumstance where the Investigator believes that it is not appropriate for the patient to participate in the study.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Study A
Clinical Evaluation of Prademagene Zamikeracel (Pz-cel) Treatment in Patients With Recessive Dystrophic Epidermolysis Bullosa (RDEB) Who Were Prescribed Pz-cel and Received Non-conforming Pz-cel in the Post-marketing Setting
Biologisk: Non-conforming pz-cel surgical application to RDEB wounds
Non-conforming pz-cel is pz-cel intended for commercial treatment that did not meet commercial release criteria, but had no safety concerns associated with its use.
Annen: Study B
Tissue Collection Study for Patients Undergoing Biopsies for Treatment With Prademagene Zamikeracel (Pz-cel)
Fremgangsmåte: Additional biopsies
Additional biopsy samples from patients who are expected to receive treatment with pz-cel in the post-marketing setting.
Eksperimentell: Study C
Post-Marketing Pz-cel Access Study in Dystrophic Epidermolysis Bullosa (DEB) Evaluating Patient Populations Not Represented in the VIITAL Clinical Trial (NCT04227106)
Biologisk: Pz-cel surgical application to DEB wounds
This intervention is for patients requiring special access for application of pz-cel.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Study A - Wound Healing ≥50%
Tidsramme: From Baseline at Week 24 (Month 6)
Proportion of RDEB wounds with healing ≥50% from Baseline at Week 24 (Month 6) as determined by direct Investigator assessment.
From Baseline at Week 24 (Month 6)
Study A - Pain Severity Scale (Wong-Baker FACES)
Tidsramme: At Week 24 (Month 6)
Pain reduction assessed by the Wong-Baker FACES Pain Rating Scale (for patients ≥6 years of age) at Week 24 (Month 6). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Week 24 (Month 6)
Study C - Wound Healing ≥50%
Tidsramme: From Baseline at Week 24 (Month 6)
Proportion of wounds with healing ≥50% from Baseline at Week 24 (Month 6) as determined by direct Investigator assessment.
From Baseline at Week 24 (Month 6)
Study C - Pain Severity Scale (Wong-Baker FACES)
Tidsramme: At Week 24 (Month 6)
Pain reduction assessed by Wong-Baker FACES Pain Rating Scale (for patients ≥6 years old) at Week 24 (Month 6). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Week 24 (Month 6)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Study A - Wound Healing ≥50%
Tidsramme: At Week 12 (Month 3)
Proportion of RDEB wounds with ≥50% healing at Week 12 (Month 3) as determined by direct Investigator assessment.
At Week 12 (Month 3)
Study A - Wound Healing ≥75%
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Proportion of RDEB wounds with ≥75% healing at Weeks 12 (Month 3) and 24 (Month 6) as determined by direct Investigator assessment.
At Weeks 12 (Month 3) and 24 (Month 6)
Study A - Wound Healing Complete
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Proportion of RDEB wounds with complete healing (i.e., re-epithelialization with no drainage or erosion and presence of only minor crusting) at Weeks 12 (Month 3) and 24 (Month 6) as determined by direct Investigator assessment.
At Weeks 12 (Month 3) and 24 (Month 6)
Study A - Pain Severity Scale (Wong-Baker FACES)
Tidsramme: At Week 12 (Month 3)
Pain reduction assessed by the Wong-Baker FACES Pain Rating Scale (for patients ≥6 years of age) at Week 12 (Month 3). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Week 12 (Month 3)
Study A - Worst Itch Severity Scale
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Change in scores of Worst Itch Numeric Rating Scale (WI-NRS; for patients ≥6 years of age) assessed at Weeks 12 (Month 3) and 24 (Month 6). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Weeks 12 (Month 3) and 24 (Month 6)
Study C - Wound Healing ≥50%
Tidsramme: At Week 12 (Month 3)
Proportion of DEB wounds with ≥50% healing at Week 12 (Month 3) as determined by direct Investigator assessment.
At Week 12 (Month 3)
Study C - Wound Healing ≥75%
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Proportion of DEB wounds with ≥75% healing at Weeks 12 (Month 3) and 24 (Month 6) as determined by direct Investigator assessment.
At Weeks 12 (Month 3) and 24 (Month 6)
Study C - Wound Healing Complete
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Proportion of DEB wounds with complete healing (i.e., re-epithelialization with no drainage or erosion and presence of only minor crusting) at Weeks 12 (Month 3) and 24 (Month 6) as determined by direct Investigator assessment.
At Weeks 12 (Month 3) and 24 (Month 6)
Study C - Pain Severity Scale (Wong-Baker FACES)
Tidsramme: At Week 12 (Month 3)
Pain reduction assessed by the Wong-Baker FACES Pain Rating Scale (for patients ≥6 years of age) at Week 12 (Month 3). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Week 12 (Month 3)
Study C - Worst Itch Severity Scale
Tidsramme: At Weeks 12 (Month 3) and 24 (Month 6)
Change in scores of WI-NRS (for patients ≥6 years of age) assessed at Weeks 12 (Month 3) and 24 (Month 6). The minimum score value is 0 and the maximum score value is 10, with the higher scores being the worse outcome.
At Weeks 12 (Month 3) and 24 (Month 6)

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Study A - The number of treatment-related cutaneous malignancies.
Tidsramme: From enrollment to Week 24
The number and incidence of treatment-related cutaneous malignancies.
From enrollment to Week 24
Study A - The number of treatment-emergent adverse events (AEs) and serious adverse events (SAEs)
Tidsramme: From enrollment to Week 24
The number and incidence of treatment-emergent adverse events (AEs) and serious adverse events (SAEs) related to pz-cel.
From enrollment to Week 24
Study A - The number of positive replication-competent retrovirus (RCR) testing results
Tidsramme: From enrollment to Week 24
The number and incidence of positive replication-competent retrovirus (RCR) testing results required for AEs and SAEs where retroviral infection is a consideration.
From enrollment to Week 24
Study A - The number of all treatment-emergent AEs and SAEs.
Tidsramme: From enrollment to Week 24
The number and incidence of all treatment-emergent AEs and SAEs.
From enrollment to Week 24
Study C - The number of treatment-related cutaneous malignancies.
Tidsramme: From enrollment to Week 24
The number and incidence of treatment-related cutaneous malignancies.
From enrollment to Week 24
Study C - The number of treatment-emergent AEs and SAEs
Tidsramme: From enrollment to Week 24
The number and incidence of treatment-emergent AEs and SAEs related to pz-cel.
From enrollment to Week 24
Study C - The number of positive RCR testing results required for AEs and SAEs
Tidsramme: From enrollment to Week 24
The number and incidence of positive RCR testing results required for AEs and SAEs where retroviral infection is a consideration.
From enrollment to Week 24
Study C - The number of all treatment-emergent AEs and SAEs.
Tidsramme: From enrollment to Week 24
The number and incidence of all treatment-emergent AEs and SAEs.
From enrollment to Week 24

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Abeona Therapeutics, Inc

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

1. november 2031

Studiet fullført (Antatt)

1. juli 2032

Datoer for studieregistrering

Først innsendt

16. juli 2026

Først innsendt som oppfylte QC-kriteriene

16. juli 2026

Først lagt ut (Faktiske)

21. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. august 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • Pz-cel-CL-402

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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