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- Registre américain des essais cliniques
- Essai clinique NCT07820085
A Study to Investigate PORT-77 Oral Dosing Compared With Placebo in Participants With Erythropoietic Protoporphyria (EPP) or X-linked Protoporphyria (XLP) (PATHWAY)
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
Statut
Intervention / Traitement
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
Inscription (Estimé)
Phase
- Phase 2
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Portal Therapeutics, Inc.
- Numéro de téléphone: 877-660-6479
- E-mail: Portal.clinical.trials@gondolabio.com
Lieux d'étude
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California
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Huntington Beach, California, États-Unis, 92647
- Recrutement
- Investigative Site
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Contact:
- Site Contact
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Ohio
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Cincinnati, Ohio, États-Unis, 43215
- Recrutement
- Investigative Site
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Contact:
- Site Contact
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
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:
- For participants aged 12 to <18 years: body weight ≥32 kg
- 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
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
Parrainer
Les enquêteurs
- Directeur d'études: Chief Medical Officer, Portal Therapeutics, Inc.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies génétiques, innées
- Maladies métaboliques
- Maladies du système digestif
- Maladies du foie
- Maladies de la peau
- Maladies de la peau, Génétique
- Porphyries hépatiques
- Porphyries
- Maladies et anomalies congénitales, héréditaires et néonatales
- Maladies nutritionnelles et métaboliques
- Maladies de la peau et du tissu conjonctif
- Protoporphyrie, érythropoïétique
- Protoporphyrie, érythropoïétique, dominant lié à l'X
Autres numéros d'identification d'étude
- PORT-77-202
- 2026-525555-86 (Numéro EudraCT)
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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