Pharmaceutical Processing World

  • Home
  • Regulatory
    • Recalls
  • Pharmaceutical Processing
  • Facility
  • Supply Chain
  • Equipment and Materials
  • Contract Manufacturing
  • Resources
    • Voices
  • Advertise
  • SUBSCRIBE

Lilly’s Taltz Psoriatic Arthritis Treatment Authorized For EU Marketing

By Eli Lilly and Company | January 26, 2018

Lilly receives EU marketing authorization for Taltz (ixekizumab) for the treatment of active psoriatic arthritis.

Eli Lilly and Company announced that the European Commission has granted marketing authorization (MA) for Taltz (ixekizumab), alone or in combination with methotrexate, for the treatment of active psoriatic arthritis (PsA) in adult patients who have responded inadequately to, or who are intolerant to, one or more disease-modifying anti-rheumatic drug (DMARD) therapies.i,ii,iii

“Psoriatic arthritis is a common inflammatory arthritis that causes serious joint pain and swelling. This makes even simple daily activities hard to do. New effective treatments which make lives better are very welcome” said Professor Bruce Kirkham, consultant rheumatologist, Guy’s and St Thomas’ NHS Foundation Trust, London.

“PsA affects up to 30 percent of people who are already living with psoriasis,iv said Arash Tahbaz, senior medical director, Eli Lilly and Company U.K. and Northern Europe. “Symptoms often begin around a decade after the onset of psoriasis, and can severely impact people’s lives and ability to work.iv We are proud to be able to offer a new treatment option that addresses both the joint and skin symptoms of PsA.”

Ixekizumab is a monoclonal antibody that selectively binds with interleukin 17A (IL-17A) cytokine and inhibits its interaction with the IL-17 receptor. This is the second approved indication for ixekizumab in the EU. Ixekizumab was authorized for the treatment of adult patients with moderate-to-severe plaque psoriasis in adults who are candidates for systemic therapy in Europe in April 2016.v
__________________________________________________________

References:

i Lilly Data on File Ref. BSD-IX-GB-0001

ii European Medicines Agency (EMA) http://www.ema.europa.eu/docs/en_GB/document_library/Summary_of_opinion/human/003943/WC500240383.pdf (accessed January 2018)

iii Lilly Data on File Ref. 36677

iv Ritchlin C, et. al. Psoriatic Arthritis. New England Journal of Medicine. 2017; 376:957-70.

v Taltz Summary of Product Characteristics.

(Source: Eli Lilly and Company via Business Wire)

 

Related Articles Read More >

This is the logo of Novartis.
Novartis breaks ground on North Carolina facility
AstraZeneca
AstraZeneca to invest $2B in Maryland, support 2,600 jobs
This is the logo of Novartis.
Novartis opens new manufacturing plant in California
samsung biologics (1)
Samsung Biologics completes Bioepis spinoff to become pure-play pharma CDMO
“ppw
EXPAND YOUR KNOWLEDGE AND STAY CONNECTED
Get the latest news, technologies, and developments in Pharmaceutical Processing.

DeviceTalks Tuesdays

DeviceTalks Tuesdays

MEDTECH 100 INDEX

Medtech 100 logo
Market Summary > Current Price
The MedTech 100 is a financial index calculated using the BIG100 companies covered in Medical Design and Outsourcing.
Pharmaceutical Processing World
  • Subscribe to our E-Newsletter
  • Contact Us
  • About Us
  • R&D World
  • Drug Delivery Business News
  • Drug Discovery & Development
  • DeviceTalks
  • MassDevice
  • Medical Design & Outsourcing
  • MEDICAL TUBING + EXTRUSION
  • Medical Design Sourcing
  • Medtech100 Index
  • R&D 100 Awards

Copyright © 2025 WTWH Media LLC. All Rights Reserved. The material on this site may not be reproduced, distributed, transmitted, cached or otherwise used, except with the prior written permission of WTWH Media
Privacy Policy | Advertising | About Us

Search Pharmaceutical Processing World

  • Home
  • Regulatory
    • Recalls
  • Pharmaceutical Processing
  • Facility
  • Supply Chain
  • Equipment and Materials
  • Contract Manufacturing
  • Resources
    • Voices
  • Advertise
  • SUBSCRIBE