Hikma update on colchicine

Hikma update on colchicine

London, 10 October 2014 - Hikma Pharmaceuticals PLC ("Hikma") (LSE: HIK) (NASDAQ Dubai: HIK) (OTC: HKMPY), the fast growing multinational pharmaceutical group, today notes that the United States District Court for the District of Delaware has granted Takeda Pharmaceuticals U.S.A., Inc.'s ("Takeda") motion for a temporary restraining order in relation to further distribution of Hikma's FDA-approved colchicine 0.6mg capsules for the prophylaxis of gout flares, while the court considers Takeda's motion for a preliminary injunction. 

Hikma received FDA approval of its New Drug Application for colchicine 0.6mg capsules on 30 September 2014.

The litigation will continue later this month and Hikma will work constructively for a positive outcome.

--  ENDS  --

Hikma Pharmaceuticals PLC                                                      
Susan Ringdal, VP Corporate Strategy and Director of Investor Relations              +44 (0)20 7399 2760
Lucinda Henderson, Deputy Investor Relations Director                                               +44 (0)20 7399 2765

FTI Consulting                                                                                 
Ben Atwell/ Matthew Cole/ Julia Phillips                                                                             +44 (0)20 3727 1000

About Hikma
Hikma Pharmaceuticals PLC is a fast growing multinational group focused on developing, manufacturing and marketing a broad range of both branded and non-branded generic and in-licensed products.  Hikma operates through three businesses: "Branded", "Injectables" and "Generics", based principally in the Middle East and North Africa ("MENA"), where it is a market leader, the United States and Europe.  In 2013, Hikma achieved revenues of $1,365 million and profit attributable to shareholders of $212 million.

This information is provided by RNS
The company news service from the London Stock Exchange


Suggested Articles

There's a lot at stake in the world of pharma litigation, and in two cases involving J&J and Gilead, attorney misconduct allegations have come up.

Without any new data, Sarepta appealed an FDA rejection and got a surprising nod for Vyondys 53—its second med approved on a surrogate marker.

The departure of BMS' Paul Biondi, who presided over an extensive deal-making strategy, adds to the challenges presented by the Celgene integration.