CompletedNot applicableNCT00004831

Study of Cysteine Hydrochloride for Erythropoietic Protoporphyria

Studying Autosomal erythropoietic protoporphyria

Last synced from ClinicalTrials.gov May 8, 2026

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Key facts

Sponsor: FDA Office of Orphan Products Development
Principal Investigator: Micheline M Mathews-Roth
St. Luke's-Roosevelt Hospital Center
Intervention: cysteine hydrochloride(drug)
Enrollment: 20 enrolled
Eligibility: 18-65 years · All sexes
Timeline: 1996 – 1998

Collaborators

St. Luke's-Roosevelt Hospital Center

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT00004831 on ClinicalTrials.gov

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