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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 settembre 2026 aggiornato da: 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

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

225

Fase

  • Fase 2
  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • California
      • Huntington Beach, California, Stati Uniti, 92647
        • Reclutamento
        • Investigative Site
        • Contatto:
          • Site Contact
    • Ohio
      • Cincinnati, Ohio, Stati Uniti, 43215
        • Reclutamento
        • Investigative Site
        • Contatto:
          • Site Contact

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Phase 2b (Treatment Group 1)
PORT-77 Dose 1
Oral tablets
Sperimentale: Phase 2b (Treatment Group 2)
PORT-77 Dose 2
Oral tablets
Comparatore placebo: Phase 2b (Treatment Group 3)
Placebo
Compresse orali
Sperimentale: Phase 3 (Treatment Group 1)
PORT-77
Oral tablets
Comparatore placebo: Phase 3 (Treatment Group 2)
Placebo
Compresse orali
Sperimentale: Phase 3 (Open-Label Extension)
PORT-77
Oral tablets

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Plasma metal-free PPIX concentration change
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Average daily time in sunlight without pain
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Chief Medical Officer, Portal Therapeutics, Inc.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

1 marzo 2029

Completamento dello studio (Stimato)

1 settembre 2029

Date di iscrizione allo studio

Primo inviato

25 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 settembre 2026

Primo Inserito (Effettivo)

15 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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