WHO ICTRP trial

DU-6859a Pharmacokinetic Study in Human

ChiCTR-ONRC-13003287 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting

Key facts

Trial ID ChiCTR-ONRC-13003287
Public title DU-6859a Pharmacokinetic Study in Human
Scientific title Pharmacokinetic Study on Sitafloxacin (DU-6859a) Tablets in Chinese Healthy Subjects
Primary sponsor Huashan Hospital affiliated to Fudan University
Registry Chinese Clinical Trial Registry (ChiCTR)
Recruitment status Not Recruiting
Study type Observational study
Phase I (Phase I study)
Countries China
Interventions Low single-dose group:Sitafloxacin 50mg tablet p.o.;Middle single-dose group:Sitafloxacin 100mg tablet p.o.;High single-dose group:Sitafloxacin 200mg tablet p.o.;Multi-dose group:Sitafloxacin 100mg tablet BID p.o. for 7 days
Registration date Apr 22, 2013
Target size Low single-dose group:12;Middle single-dose group:12;High single-dose…
Registry page chictr.org.cn

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations