Phase III Study of L-Cysteine in Patients With Erythropoietic Protoporphyria
NCT00004940 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2015-03-25
Summary
OBJECTIVES:
I. Determine the long-term efficacy and safety of L-cysteine in the prevention photosensitivity in patients with erythropoietic protoporphyria.
Conditions
Interventions
- DRUG
-
cysteine hydrochloride
Sponsors & Collaborators
-
Brigham and Women's Hospital
lead OTHER
Principal Investigators
-
Micheline Mary Mathews-Roth · Brigham and Women's Hospital
Study Design
- Purpose
- TREATMENT
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1996-05-31
- Completion
- 2001-09-30
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