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A Study to Investigate PORT-77 Oral Dosing Compared With Placebo in Participants With Erythropoietic Protoporphyria (EPP) or X-linked Protoporphyria (XLP) (PATHWAY)

10 de septiembre de 2026 actualizado por: Portal Therapeutics, Inc.

A Phase 2b/3, Quadruple-Blinded, Randomized, Placebo-Controlled Study of PORT-77 Administered Orally to Adults and Adolescents With Erythropoietic Protoporphyria or X-Linked Protoporphyria and an Open-Label Extension

PATHWAY is a Phase 2b/3 clinical study with an Open-Label Extension (OLE). It tests PORT-77 in patients with EPP, EPP2, and XLP.

The study has three parts:

Part 1: Phase 2b

  • Find the right dose of PORT-77 to lower PPIX levels in the blood
  • Test if PORT-77 lowers PPIX levels better than placebo
  • Check the safety of each dose

Part 2: Phase 3

  • Test if PORT-77 lowers PPIX levels better than placebo
  • Test if PORT-77 increases the amount of time patients spend in sunlight each day without pain compared to placebo
  • Check the safety of PORT-77

Part 3: Open-Label Extension (OLE)

  • Test the long-term effect of PORT-77 on PPIX levels and time in sun
  • Monitor long-term safety

Descripción general del estudio

Descripción detallada

PATHWAY is a Phase 2b/3, multiregional, multicenter clinical study of PORT-77 in adults and adolescents with EPP or XLP. The study consists of 3 parts: Part 1 (Phase 2b), Part 2 (Phase 3), and Part 3 (OLE).

Part 1 and Part 2 are randomized, quadruple-blinded, placebo-controlled studies. Part 1 is a Phase 2b study evaluating the safety, tolerability, and preliminary efficacy of 2 dose levels of PORT-77. Part 2 is a Phase 3 study designed to confirm the efficacy of the selected PORT-77 dose and to further characterize safety in a larger cohort. All participants who complete Part 1 or Part 2 of the study will have the opportunity to enroll in Part 3 (OLE).

Tipo de estudio

Intervencionista

Inscripción (Estimado)

225

Fase

  • Fase 2
  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • California
      • Huntington Beach, California, Estados Unidos, 92647
        • Reclutamiento
        • Investigative Site
        • Contacto:
          • Site Contact
    • Ohio
      • Cincinnati, Ohio, Estados Unidos, 43215
        • Reclutamiento
        • Investigative Site
        • Contacto:
          • Site Contact

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Aged 12 years or older.
  • Clinical history of EPP, XLP, or EPP2 supported by genetic confirmation or historical laboratory test results
  • History of consistent, non-painful prodrome within approximately 45 minutes of sunlight exposure and prior to phototoxic attacks
  • Demonstrates ≥85% compliance with daily symptom diary during run-in period.
  • Body weight or BMI at Screening as follows:

    1. For participants aged 12 to <18 years: body weight ≥32 kg
    2. For participants aged ≥18 years: BMI ≥18.5 kg/m2
  • AST and ALT <3 × ULN and total bilirubin <2 × ULN (unless documented Gilbert syndrome) at Screening
  • Willing and able to provide informed consent and/or assent for the study.
  • Willing and able to comply with study visits, study procedures, and contraception guidance
  • Intends to remain in the same approximate geographic latitude for the duration of the placebo-controlled period, with no more than 14 days spent outside this region.

Exclusion Criteria:

  • Diagnosis of another porphyria or another photodermatosis that may confound the evaluation of PORT-77
  • Any evidence of clinically significant organ dysfunction or any clinically significant deviation from normal in the clinical or laboratory assessments
  • Major surgery within 8 weeks before Screening, incomplete recovery from any previous surgery, or major surgery planned to occur during the study
  • History of, or anticipated need for, liver transplantation or history of bone marrow transplantation
  • Active infection with hepatitis B or C
  • Unable to swallow tablets or has a disease that significantly affects gastrointestinal function
  • Any other disease, condition, or circumstance that, at the discretion of the Investigator or Sponsor, would interfere with the evaluation of PORT-77 or study participation, or would make study participation not in the best interest of the participant
  • History of drug or alcohol abuse within the last 12 months, or current or planned use of prohibited or illegal substances
  • Has taken any medication, vitamin, or supplement that alters sensitivity to light exposure (eg, afamelanotide, melanotan, beta carotene, dersimelagon) within 90 days of Day 1; or has taken bitopertin within 120 days of Day 1; or has taken iron within 30 days of Day 1
  • Drugs or supplements that may impact or be impacted by PORT-77
  • Concurrent or anticipated participation in an interventional clinical trial during the study period.
  • Received another investigational therapy within 5 half-lives, if the half-life is known, or within 30 days, if the half-life is unknown, prior to Day 1.
  • Known hypersensitivity to PORT-77 or excipients
  • Female who has a positive pregnancy test at Screening or Day 1 or is breastfeeding

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Phase 2b (Treatment Group 1)
PORT-77 Dose 1
Oral tablets
Experimental: Phase 2b (Treatment Group 2)
PORT-77 Dose 2
Oral tablets
Comparador de placebos: Phase 2b (Treatment Group 3)
Placebo
Tabletas orales
Experimental: Phase 3 (Treatment Group 1)
PORT-77
Oral tablets
Comparador de placebos: Phase 3 (Treatment Group 2)
Placebo
Tabletas orales
Experimental: Phase 3 (Open-Label Extension)
PORT-77
Oral tablets

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Plasma metal-free PPIX concentration change
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Characterize the dose-response of PORT-77 on plasma PPIX levels compared to placebo
Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Adverse Events
Periodo de tiempo: Part 1 - Day 1 through Day 84; Part 2 - through Day 182; Part 3 - through Month 12
Evaluate safety and tolerability of each dose of PORT-77 over the course of the study
Part 1 - Day 1 through Day 84; Part 2 - through Day 182; Part 3 - through Month 12
Average daily time in sunlight without pain
Periodo de tiempo: Part 2 - Day 155 through 182
Assess the effect of different doses of PORT-77 on average daily time in sunlight without pain compared to placebo
Part 2 - Day 155 through 182

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Average daily time in sunlight without pain
Periodo de tiempo: Part 1 - Days 57 through 84
Assess the effect of different doses of PORT-77 on average daily time in sunlight without pain compared to placebo
Part 1 - Days 57 through 84
Change from baseline in daily time in sunlight before first prodromal symptom
Periodo de tiempo: Part 1 - Day 1 through Day 84; Part 2 - through Day 182
Assess the effect of different doses of PORT-77 on average daily time in sunlight before first prodromal symptom compared to placebo
Part 1 - Day 1 through Day 84; Part 2 - through Day 182
Cumulative total time in sunlight without pain
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Assess the effect of different doses of PORT-77 on cumulative total time in sunlight without pain compared to placebo
Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Number and severity of phototoxic reactions
Periodo de tiempo: Part 1 - Day 1 through 84; Part 2 - through Day 182; through Month 12
Assess the effect of different doses of PORT-77 on the rate and severity of phototoxic reactions compared to placebo
Part 1 - Day 1 through 84; Part 2 - through Day 182; through Month 12
Change from baseline in validated QoL scores - PGI-C
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12

Evaluate the effect of PORT-77 on the Patient Global Impressions - Change in clinical status (PGI-C) in adults compared to placebo.

The PGI-C measures Change in clinical status. Higher numerical scores (1-7) in PGI-C indicate worsening of clinical status.

Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Change from baseline in validated QoL scores - PGI-S
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12

Evaluate the effect of PORT-77 on the Patient Global Impressions - Severity of clinical status.

The PGI-S measures Severity of clinical status. Higher numerical scores in PGI-S (1-5) indicate greater symptom severity.

Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Change from baseline in validated QoL scores - SF36
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12

Evaluate the effect of PORT-77 on the Short Form 36 Health Survey (SF-36) in adults compared to placebo.

The SF-36 covers 36 individual items that evaluate functional health and well-being. It produces eight health domain scores and two summary component scores (Physical Component Summary and Mental Component Summary) where higher values (0-100) represent better health.

Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Change from baseline in validated QoL scores - PedsQL
Periodo de tiempo: Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12

Evaluate the effect of PORT-77 on the Pediatric Quality of Life Inventory (PedsQL) in adolescents compared to placebo.

The (PedsQL) evaluates four main domains: physical functioning, emotional functioning, social functioning, and school functioning. It uses a 0 to 100 scale where higher scores show a better health-related quality of life.

Part 1 - Days 1 through 84; Part 2 - through Day 182; Part 3 - through Month 12
Area under the curve (AUCtau) of PORT-77
Periodo de tiempo: Part 1 - Day 1 through 84; Part 2 - through Day 182
Model derived area under the curve of PORT-77 during dosing interval at steady state
Part 1 - Day 1 through 84; Part 2 - through Day 182
Cmax of PORT-77
Periodo de tiempo: Part 1 - Day 1 through 84; Part 2 - through Day 182
Model derived maximal concentration after dosing of PORT-77 at steady state
Part 1 - Day 1 through 84; Part 2 - through Day 182
Ctrough of PORT-77
Periodo de tiempo: Part 1 - Day 1 through 84; Part 2 - through Day 182
Model derived trough concentration after dosing of PORT-77 at steady state
Part 1 - Day 1 through 84; Part 2 - through Day 182

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Director de estudio: Chief Medical Officer, Portal Therapeutics, Inc.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de marzo de 2029

Finalización del estudio (Estimado)

1 de septiembre de 2029

Fechas de registro del estudio

Enviado por primera vez

25 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

10 de septiembre de 2026

Publicado por primera vez (Actual)

15 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

10 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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