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

Cardiac Safety and Trauma Trial Design Subject Of Hemopure Advisory Committee

This article was originally published in The Pink Sheet Daily

Executive Summary

FDA’s Blood Products Advisory Committee review could give the agency the green light to lift the clinical hold on the hemoglobin-based oxygen therapeutic.

You may also be interested in...



U.S. Navy Plans To Proceed With Hemopure Development

Following negative review by FDA advisory committee, Navy will work on a revised clinical trial protocol for a scaled-down Phase II study.

U.S. Navy Plans To Proceed With Hemopure Development

Following negative review by FDA advisory committee, Navy will work on a revised clinical trial protocol for a scaled-down Phase II study.

Sen. Grassley Presses HHS On Ethics Of FDA-Approved Blood Substitute Study

Grassley wants an investigation into FDA’s approval of a protocol that allowed patients to be treated with a blood substitute even though blood was available.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS063530

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