Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02774057Phase 4Unknown
Phase 4, randomised, open-label trial (2 arms), sponsored by American University of Beirut Medical Center. Primary endpoint: Tolerability to Iron sulfate and Captafer® at 6 weeks. Status: unknown.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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