Kiadis may pursue EMA submission in blood cancer earlier than expected

28 March 2017
2019_biotech_test_vial_discovery_big

European regulators have accepted Kiadis Pharma’s (AMS: KDS) Pediatric Investigation Plan (PIP) for ATIR101 (allodepleted T-cell immunotherapeutics), an important regulatory milestone.

In addition, regulators informed the Dutch company it may defer the initiation of certain studies defined in the PIP until after it files for regulatory approval, bringing forward considerably the likely application date.

Shares in the biopharmceutical specialists are trading around 2% higher in Amsterdam.

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

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology