Pink Sheet 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

A Skeptical Take on Current Alzheimer’s Therapy: FDA’s Temple Says Problem Is Drugs, Not Endpoints

This article was originally published in RPM Report

Executive Summary

When it comes to Alzheimer’s Drug development, FDA’s Bob Temple firmly believes regulatory standards are not the problem. “You just need a drug that works.”

Advertisement

Related Content

A New Direction For Alzheimer’s R&D: FDA Outlines Early Disease Pathway
A New Direction for Alzheimer’s R&D: FDA Outlines Early Disease Pathway
Invaluable Guidance: FDA’s Dean of Drug Reviews on “Enrichment Strategies”
Lilly Antibody Proves Ineffective In Rheumatoid Arthritis, But Lupus Trials Continue

Topics

Advertisement
UsernamePublicRestriction

Register

PS081083

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