Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06837155Phase 1Completed
Phase 1, randomised trial of TS-172 in hyperphosphatemia (4 arms), sponsored by Taisho Pharmaceutical. Primary endpoint: QT-interval corrected by Fridericia corrections in Holter ECGs at 24 hours. Started Mar 2025; status: completed.
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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