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TMG-123 Phase 2 study

Placebo-Controlled, Double-Blind, Randomized, Parallel-Group, Exploratory Study of TMG-123 in Patients with Type 2 Diabetes Mellitus

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223642
Enrollment
90
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 : 4

Sponsors

TEIJIN PHARMA LIMITED
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes mellitus

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Changes in HbA1c levels at 12 weeks after the start of drug administration

Secondary

MeasureTime frame
Changes in glucose related parameters at 12 weeks and 24 weeks, Safety, PK

Outcome results

None listed

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