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A Phase I study of TMG-123, 7 days repeat administraiton

Placebo-controlled, double-blind, repeated oral dose, clinical pharmacology study of TMG-123 in patients with type 2 diabetes mellitus

Status
Unknown
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223650
Enrollment
36
Registered
2017-09-05
Start date
2017-09-05
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

Type 2 diabetes mellitus

Interventions

investigational material(s) Generic name etc : TMG-123 INN of investigational material : Therapeutic category code : 396 Antidiabetic agents Dosage and Administration for Investigational material : 8

Sponsors

TEIJIN PHARMA LIMITED
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes mellitus

Exclusion criteria

Exclusion criteria: Subjects with type 1 diabetes mellitus or diabetes due to other specific mechanisms or diseases Subjects judged as not eligible by the investigator or sub-investigators for other reasons

Outcome results

None listed

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