Pink Sheet is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

CIBA-GEIGY's ESTRADERM (ESTRODIAL) TRANSDERMAL PATCH

Executive Summary

CIBA-GEIGY's ESTRADERM (ESTRODIAL) TRANSDERMAL PATCH for treatment of menopausal symptoms was approved by FDA Sept. 10. The product is available in dosages of 0.05 mg and 0.1 mg to be applied twice weekly. Estraderm is Ciba-Geigy's third transdermal patch product utilizing Alza's delivery system. Ciba's Transderm Scop (scopolamine) was the first transdermal product on the market, followed by three nitroglycerin patches, of which Transderm-Nitro is the market leader. Estraderm is the third drug class to be made available in a transdermal delivery system. Boehringer Ingelheim's antihypertensive Catapres (clonidine) is the only other product line besides nitroglycerin. Ciba-Geigy obtained approval for Estraderm two years after an NDA submission in August 1984. FDA's Fertility and Maternal Health Drugs Advisory Cmte. recommended it for approval last December. The transdermal estrogen product is currently in clinicals for osteoporosis.

You may also be interested in...



Part D Discount Liability Coming Into Focus: CMS Releases Drug Cost Data

Newly released Medicare Part D data sheds light on the sales hit that branded pharmaceutical manufacturers will face when the coverage gap discount program gets under way in 2011

FDA Skin Infections Guidance Spurs Debate On Endpoint Relevance

FDA appears headed for a showdown with clinicians and the pharmaceutical industry over the proposed new clinical trial endpoints for acute bacterial skin and skin structure infections, the guidance's approach for justifying a non-inferiority margin and proposed changes in the types of patients that should be enrolled in trials

Shire Hopes To Sow Future Deals With $50M Venture Fund

Specialty drug maker Shire has quietly begun scouting deals with a brand-new $50 million venture fund, the latest of several in-house investment arms to launch with their parent company's pipelines, not profits, as the measure of their worth

Latest Headlines
See All
UsernamePublicRestriction

Register

PS010713

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel