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

FTC sues Enforma

This article was originally published in The Tan Sheet

Executive Summary

Civil contempt charges filed by FTC Jan. 3 against Enforma Natural Products; hearing is scheduled for Feb. 4 in Los Angeles federal court. Commission alleges Enforma "blatantly disregarded" a May 2000 order by continuing to make unsubstantiated claims about its Fat Trapper Plus and Exercise In A Bottle weight-loss products (1"The Tan Sheet" May 1, 2000, p. 17). FTC requests order requiring defendants cease use of trade names Fat Trapper, Fat Trapper Plus and Exercise in a Bottle, and turn over all gross revenues from sale of products at issue since May 2000...

You may also be interested in...



Enforma To Cease Deceptive Weight Loss Claims, Pay $10 Mil. -FTC

Enforma Natural Products settles Federal Trade Commission charges that it made false and unsubstantiated weight loss claims in an infomercial and on the Internet, without admitting a violation of law, the agency announces April 26.

Alvotech Highlights Lack Of Simponi Rivals As It Delivers Golimumab Results

Alvotech has just become the first company to announce positive topline results from a confirmatory clinical study for a proposed golimumab rival to Simponi and Simponi Aria – and moreover, the firm sees limited competition from other biosimilars on the horizon.

Xbrane Assembles The Troops As FDA Says No To Lucentis Biosimilar

Xbrane Biopharma was riding the crest of a wave with the EU launch of its biosimilar to Lucentis, following years of toil and investment. However, plans to roll out the product in the US will have to be pushed back – likely – into the middle of 2025, following a US FDA complete response letter.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS093494

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