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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 septembre 2026 mis à jour par: 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

Aperçu de l'étude

Description détaillée

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).

Type d'étude

Interventionnel

Inscription (Estimé)

225

Phase

  • Phase 2
  • Phase 3

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • California
      • Huntington Beach, California, États-Unis, 92647
        • Recrutement
        • Investigative Site
        • Contact:
          • Site Contact
    • Ohio
      • Cincinnati, Ohio, États-Unis, 43215
        • Recrutement
        • Investigative Site
        • Contact:
          • Site Contact

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Phase 2b (Treatment Group 1)
PORT-77 Dose 1
Oral tablets
Expérimental: Phase 2b (Treatment Group 2)
PORT-77 Dose 2
Oral tablets
Comparateur placebo: Phase 2b (Treatment Group 3)
Placebo
Comprimés oraux
Expérimental: Phase 3 (Treatment Group 1)
PORT-77
Oral tablets
Comparateur placebo: Phase 3 (Treatment Group 2)
Placebo
Comprimés oraux
Expérimental: Phase 3 (Open-Label Extension)
PORT-77
Oral tablets

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Plasma metal-free PPIX concentration change
Délai: 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
Délai: 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
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Average daily time in sunlight without pain
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Directeur d'études: Chief Medical Officer, Portal Therapeutics, Inc.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 mars 2029

Achèvement de l'étude (Estimé)

1 septembre 2029

Dates d'inscription aux études

Première soumission

25 août 2026

Première soumission répondant aux critères de contrôle qualité

10 septembre 2026

Première publication (Réel)

15 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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