Brief: Poland And U.K. Regulatory Authorities Approve Use Of New, Higher-Yielding Manufacturing Process For Nomacopan In Pivotal Clinical Study
March 29 (Reuters) - Akari Therapeutics PLC AKTX.O :
* POLAND AND U.K. REGULATORY AUTHORITIES – URPL AND MHRA –
APPROVE
USE OF NEW, HIGHER-YIELDING MANUFACTURING PROCESS FOR NOMACOPAN
IN PIVOTAL CLINICAL STUDY
* AKARI THERAPEUTICS PLC - PHASE 3 STUDY OF NOMACOPAN IN
PEDIATRIC
HSCT-TMA INCLUDES CLINICAL TRIAL SITES IN POLAND, U.K. AND U.S
Source text for Eikon: ID:nGNX6xfDyy
Further company coverage: AKTX.O
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Akari Therapeutics
See all newsBrief: Akari Therapeutics - Aktx-101 Demonstrates Robust Anti-Tumor Activity In Urothelial Cancer Preclinical Models
UK's Akari Therapeutics Q2 net loss widens on higher R&D for AKTX-101
Akari Therapeutics PLC reports results for the quarter ended June 30 - Earnings Summary
Akari Therapeutics PLC expected to post a loss of $1.40 a share - Earnings Preview
Brief: Akari Therapeutics Enters Strategic Research Collaboration With Whitehawk Therapeutics