Lederle Laboratories and Procter & Gamble have launched Ziac (bisoprolol fumarate and hydrochloro-thiazide) in the USA for the initial treatment of mild to moderate hypertension. The once-a-day product is the first low-dose, two-component antihypertensive developed specifically to address dose-related side effects, according to Lederle.
Ziac is available in 2.5mg, 5mg, and 10mg doses of bisoprolol, each with 6.25mg hydrochlorothiazide. The drug is suitable for newly-diagnosed patients, those who are not adequately controlled or who are having side effects with their present therapy, and patients who experience significant potassium loss with hydrochlorothiazide therapy.
Linda Wase, vice president of scientific affairs at Lederle, said that the beta blocker/diuretic combination in Ziac complement each other and act synergistically to lower blood pressure, while minimizing the side effects seen when the drugs are taken separately at higher doses. Two multicenter studies have shown that Ziac provides adequate hypotensive cover with side effects comparable to placebo.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze