Phase 2, Double-Blind, Parallel-group Study of S-2367 in Obese Patients

Status

Unknown

Phases

Phase 2

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT2080221077

Enrollment

280

Registered

2010-04-22

Start date

2010-04-22

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

Obesity (BMI:>=25.0) with glucose intolerance or type 2 diabetes and dyslipidemia

Interventions

investigational material(s) Generic name etc : S-2367 INN of investigational material : Therapeutic category code : 119 Other agents affecting central nervous system Dosage and Administration for Inv

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Main inclusion criteria 1. With BMI >=25.0 2. With visceral fat area >=100 cm2 as determined with abdominal CT 3. Previously diagnosed with glucose intolerance or type 2 diabetes, and HbA1c >=6.1% to =150 mg/dL and/or fasting serum HDL-cholesterol <40 mg/dL

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Percent change in body weight	—

Outcome results

None listed

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