KRP-AM1977X Phase III Comparative Study (sinusitis)

KRP-AM1977X PhaseIII Clinical Study-Double blind comparative study for the patients with sinusitis-

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT2080222862

Enrollment

250

Registered

2015-05-25

Start date

2015-06-26

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sinusitis (severity of infection: moderate to severe)

Interventions

investigational material(s) Generic name etc : KRP-AM1977X Tablet INN of investigational material : lascufloxacin Therapeutic category code : 624 Synthetic antibacterials Dosage and Administration for

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Sinusitis with clear infection symptoms

Exclusion criteria

Exclusion criteria: Sinusitis patient except Fungal Rhinosinusitis, eosinophilic sinusitis, etc. Patient with serious functional disorder that would unsuitable for the study Patient showing the tendency to improve sinusitis symptoms by other agents etc.

Design outcomes

Primary

Measure	Time frame
efficacy Clinical efficacy at the end of treatment	—

Secondary

Measure	Time frame
efficacy Recurrence rate at the test of cure, etc.	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026