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Clinical Trials associated with TRC-041266Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicentre Study to Evaluate the Efficacy and Safety of TRC041266 Compared to Placebo in Patients With Chronic Stable Heart Failure, an LVEF ≥40%, Moderate to Severe Diastolic Dysfunction and Type 2 Diabetes Mellitus
This study will be conducted as a randomized, multi-centre, double-blind, parallel-group, placebo-controlled study in patients receiving SoC therapy. Eligible participants will be randomized in a ratio of 1:1 to receive either test product, TRC041266 1500 mg or matching placebo twice daily for 48 weeks
/ Not yet recruitingPhase 1IIT An Open Label, Randomized, Multiple-dose, Crossover Study to Compare the OralPharmacokinetics and Safety of TRC041266 Powder with TRC4186 Tablet in HealthyHuman Subjects.
Start Date01 Jul 2020 |
Sponsor / Collaborator- |
An Open Label, Randomized, Crossover Study to Compare the Pharmacokinetics of TRC041266 Powder with TRC4186 Tablet under Fasting Condition and to Evaluate the Effect of Food on the Pharmacokinetics of TRC041266 Powder in Healthy Human Subjects
Start Date10 Aug 2018 |
Sponsor / Collaborator- |
100 Clinical Results associated with TRC-041266
100 Translational Medicine associated with TRC-041266
100 Patents (Medical) associated with TRC-041266
100 Deals associated with TRC-041266