Citius set back in bid to revive med for rare form of non-Hodgkin's

31 July 2023
citius-pharma-large-1

The US Food and Drug Administration has dealt a blow to the market value of New Jersey, USA-based oncology company Citius Pharmaceuticals (Nasdaq: CTXR).

Ahead of the opening bell on Monday, shares in the company had fallen by over a fifth, following news of a Complete Response Letter (CRL) related to its regulatory submission for denileukin diftitox, also known as Lymphir.

Citius is developing the interleukin (IL)-2-diphtheria toxin fusion protein to treat people with relapsed or refractory cutaneous T-cell lymphoma (CTCL), after at least one prior systemic therapy.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Biotechnology