X-Linked Protoporphyria (XLP)

2

Review clinical trials related to X-Linked Protoporphyria (XLP). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Available

Expanded Access Program of Bitopertin For Participants With EPP or XLP

The goal of this expanded access program is to provide bitopertin to patients with EPP and XLP who have no satisfactory treatment options available in the US and to learn if bitopertin is safe to treat EPP and XLP.

Trial details
Age: 12+Biological sex: AllType: Expanded AccessSponsor: Disc Medicine, IncUpdated: Oct 6, 2026Locations: 7
Eligibility criteria

Written informed consent (and assent where applicable). [+4]

Known hypersensitivity to bitopertin or its excipients. [+13]

Status: Recruiting

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

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

Participants needed: 225
Trial details
Phase: Phase 2, Phase 3Age: 12+Biological sex: AllType: InterventionalSponsor: Portal Therapeutics, Inc.Updated: Sep 15, 2026Locations: 2
Eligibility criteria

Aged 12 years or older. [+9]

Diagnosis of another porphyria or another photodermatosis that may confound the... [+13]