Medtech Insight is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

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
UsernamePublicRestriction

Selzentry Faces Assay Challenge Even After Advisory Committee Thumbs Up

This article was originally published in The Pink Sheet Daily

Executive Summary

FDA will wrestle with how to include an unapproved diagnostic test in expanded labeling for Pfizer's HIV drug.
Advertisement

Related Content

FDA Expands Selzentry Indication, But Ties Use To Screening With "Highly Sensitive" Assay
FDA Expands Selzentry Indication, But Ties Use To Screening With "Highly Sensitive" Assay
Selzentry Advisory Committee To Weigh Virologic Resistance Vs. Adverse Events
Selzentry Advisory Committee To Weigh Virologic Resistance Vs. Adverse Events

Topics

Advertisement
UsernamePublicRestriction

Register

PS068716

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

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