Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide 100 mg/25 mg Tablet Under Fasted Conditions

Completed · Not applicable

Conditions studied: Hypertension

In brief

The objective of this study was to prove the bioequivalence of Losartan Potassium/Hydrochlorothiazide 100/25 mg tablet under fasted conditions.

Key facts

Study ID

NCT01102478

Run by

Roxane Laboratories

People needed

30

Starts

2005-02-01

Expected to finish

2005-03-01

Last updated by the study team

2018-01-23

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening.

You may not qualify if…

• Positive test for HIV, Hepatitis B, or Hepatitis C.
• Treatment with known enzyme altering drugs.
• History of allergic or adverse response to losartan potassium hydrochlorothiazide or any comparable or similar product.

Where it is running

• CEDRA Clinical Research, LLC — Austin, Texas, United States

Full record on ClinicalTrials.gov

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