- ICH GCP
- USA klinikai vizsgálatok nyilvántartása
- Klinikai vizsgálat 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
A tanulmány áttekintése
Állapot
Beavatkozás / kezelés
Részletes leírás
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).
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 2. fázis
- 3. fázis
Kapcsolatok és helyek
Tanulmányi kapcsolat
- Név: Portal Therapeutics, Inc.
- Telefonszám: 877-660-6479
- E-mail: Portal.clinical.trials@gondolabio.com
Tanulmányi helyek
-
-
California
-
Huntington Beach, California, Egyesült Államok, 92647
- Toborzás
- Investigative Site
-
Kapcsolatba lépni:
- Site Contact
-
-
Ohio
-
Cincinnati, Ohio, Egyesült Államok, 43215
- Toborzás
- Investigative Site
-
Kapcsolatba lépni:
- Site Contact
-
-
Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
- Gyermek
- Felnőtt
- Idősebb felnőtt
Egészséges önkénteseket fogad
Leírás
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
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Kezelés
- Kiosztás: Véletlenszerűsített
- Beavatkozó modell: Párhuzamos hozzárendelés
- Maszkolás: Négyszeres
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
|---|---|
|
Kísérleti: Phase 2b (Treatment Group 1)
PORT-77 Dose 1
|
Oral tablets
|
|
Kísérleti: Phase 2b (Treatment Group 2)
PORT-77 Dose 2
|
Oral tablets
|
|
Placebo Comparator: Phase 2b (Treatment Group 3)
Placebo
|
Orális tabletták
|
|
Kísérleti: Phase 3 (Treatment Group 1)
PORT-77
|
Oral tablets
|
|
Placebo Comparator: Phase 3 (Treatment Group 2)
Placebo
|
Orális tabletták
|
|
Kísérleti: Phase 3 (Open-Label Extension)
PORT-77
|
Oral tablets
|
Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
|
Plasma metal-free PPIX concentration change
Időkeret: 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
Időkeret: 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
Időkeret: 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
|
Másodlagos eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
|
Average daily time in sunlight without pain
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
|
Együttműködők és nyomozók
Szponzor
Nyomozók
- Tanulmányi igazgató: Chief Medical Officer, Portal Therapeutics, Inc.
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Becsült)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
Kulcsszavak
További vonatkozó MeSH feltételek
- Genetikai betegségek, veleszületett
- Anyagcsere-betegségek
- Emésztőrendszeri betegségek
- Májbetegségek
- Bőrbetegségek
- Bőrbetegségek, genetikai
- Porphyrias, máj
- Porphyrias
- Veleszületett, örökletes és újszülöttkori betegségek és rendellenességek
- Táplálkozási és anyagcsere-betegségek
- Bőr- és kötőszöveti betegségek
- Protoporfiria, eritropoetikus
- Protoporphyria, eritropoietikus, X-kapcsolt domináns
Egyéb vizsgálati azonosító számok
- PORT-77-202
- 2026-525555-86 (EudraCT szám)
Terv az egyéni résztvevői adatokhoz (IPD)
Tervezi megosztani az egyéni résztvevői adatokat (IPD)?
Gyógyszer- és eszközinformációk, tanulmányi dokumentumok
Egy amerikai FDA által szabályozott gyógyszerkészítményt tanulmányoz
Egy amerikai FDA által szabályozott eszközterméket tanulmányoz
Ezt az információt közvetlenül a clinicaltrials.gov webhelyről szereztük be, változtatás nélkül. Ha bármilyen kérése van vizsgálati adatainak módosítására, eltávolítására vagy frissítésére, kérjük, írjon a következő címre: register@clinicaltrials.gov. Amint a változás bevezetésre kerül a clinicaltrials.gov oldalon, ez a webhelyünkön is automatikusan frissül. .