SYR-472 Open-label Study

NCT01751360 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2023-12-11

No results posted yet for this study

Summary

To evaluate the efficacy and safety of treatment with SYR-472 in diabetic patients.

Conditions

Interventions

DRUG

SYR-472

Sponsors & Collaborators

Principal Investigators

  • General Manager · Takeda (Note: This product was divested to Teijin Pharma Limited in 2023)

Study Design

Purpose
TREATMENT

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-01
Primary Completion
2013-08-01
Completion
2013-08-01

Countries

  • Japan

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01751360 on ClinicalTrials.gov