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A Randomised, Double-blind, Placebo-controled Parallel Group Efficacy and Safety Study of BI 1356 (5 mg Administered Orally Once Daily) Over 24 Weeks, in Drug Naive or Previously Treated (6 Weeks Washout) Type 2 Diabetic Patients With Insufficient Glycemic Control

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DataCite Commons2025-12-08 更新2026-05-07 收录
下载链接:
https://search.vivli.org/doiLanding/studies/00003511/isLanding
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资源简介:
To investigate efficacy, safety and tolerability of BI 1356 versus placebo
提供机构:
Vivli
创建时间:
2019-04-12
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