Investors Hangout Stock Message Boards Logo
  • Mailbox
  • Favorites
  • Boards
    • The Hangout
    • NASDAQ
    • NYSE
    • OTC Markets
    • All Boards
  • Whats Hot!
    • Recent Activity
    • Most Viewed Boards
    • Most Viewed Posts
    • Most Posted
    • Most Followed
    • Top Boards
    • Newest Boards
    • Newest Members
  • Blog
    • Recent Blog Posts
    • Recently Updated
    • News
    • Stocks
    • Crypto
    • Investing
    • Business
    • Markets
    • Economy
    • Real Estate
    • Personal Finance
  • Market Movers
  • Interactive Charts
  • Login - Join Now FREE!
  1. Home ›
  2. Stock Message Boards ›
  3. Stock Boards ›
  4. CytoDyn Inc (CYDY) Message Board

On March 11th, 2020 Dr. Lalezari emailed Jeff Murr

Message Board Public Reply | Private Reply | Keep | Replies (4)                   Post New Msg
Edit Msg () | Previous | Next


Post# of 153839
(Total Views: 1250)
Posted On: 11/06/2023 9:49:41 AM
Posted By: ohm20
On March 11th, 2020 Dr. Lalezari emailed Jeff Murray (FDA Deputy Director of the Division of Antiviral Products) about Covid-19 trials using leronlimab and the protocols. His response -

Quote:
As an investigator, why would you choose this drug rather than be involved with either the NIH or Gilead remdesivir trials? Remdesivir has decent in-vitro activity against SARS CoV-2, one of the few drugs tested so far. What compelling non-clinical data support the use of leronlimab for COVID-19 over other drugs that have been prioritized? In addition we are not enthused about single arm trials or compassionate use for products that don't have good evidence of activity nor for drugs that might have unfavorable toxicity profiles (the latter is not the case for leronlimab).



It seems like the fix was in for remdesivir quite early. At least someone at the FDA knew leronlimab's safety.

When the data from the Covid-19 patients at Montefiore became available Dr. Lalezari sent it to Jeff Murray. I'm sure he also outlined the mechanism of action. Part of his response -

Quote:
"In my opinion, leronlimab didn't have the type of compelling nonclinical rationale to give me a strong Bayesian prior, so it will take a lot more than a series of 7 patients (who did not fit the definition of critically ill) to change my opinion.



Does Murray know so little that he only knows CCR5 in the context of HIV? It seems like the FDA mainly consists of bureacrats who have little knowledge of science and will avoid obtaining any.

PS. Jeff Murray left the FDA and became an advisor for Exavir Therapeutics who's main area is HIV.



(20)
(0)




CytoDyn Inc (CYDY) Stock Research Links


  1.  
  2.  


  3.  
  4.  
  5.  






Investors Hangout

Home

Mailbox

Message Boards

Favorites

Whats Hot

Blog

Settings

Privacy Policy

Terms and Conditions

Disclaimer

Contact Us

Whats Hot

Recent Activity

Most Viewed Boards

Most Viewed Posts

Most Posted Boards

Most Followed

Top Boards

Newest Boards

Newest Members

Investors Hangout Message Boards

Welcome To Investors Hangout

Stock Message Boards

American Stock Exchange (AMEX)

NASDAQ Stock Exchange (NASDAQ)

New York Stock Exchange (NYSE)

Penny Stocks - (OTC)

User Boards

The Hangout

Private

Global Markets

Australian Securities Exchange (ASX)

Euronext Amsterdam (AMS)

Euronext Brussels (BRU)

Euronext Lisbon (LIS)

Euronext Paris (PAR)

Foreign Exchange (FOREX)

Hong Kong Stock Exchange (HKEX)

London Stock Exchange (LSE)

Milan Stock Exchange (MLSE)

New Zealand Exchange (NZX)

Singapore Stock Exchange (SGX)

Toronto Stock Exchange (TSX)

Contact Investors Hangout

Email Us

Follow Investors Hangout

Twitter

YouTube

Facebook

Market Data powered by QuoteMedia. Copyright © 2025. Data delayed 15 minutes unless otherwise indicated (view delay times for all exchanges).
Analyst Ratings & Earnings by Zacks. RT=Real-Time, EOD=End of Day, PD=Previous Day. Terms of Use.

© 2025 Copyright Investors Hangout, LLC All Rights Reserved.

Privacy Policy |Do Not Sell My Information | Terms & Conditions | Disclaimer | Help | Contact Us