
Cellmid 2017 Annual Report
12
CEO
REPORT
CONTINUED
LYRAMID’S DIAGNOSTIC PATENTS CONTINUE 
TO DELIVER REVENUE
Lyramid’s diagnostic patents have been licensed to three 
groups; Quest, Pacific Edge and Fujikura Kasei. Pacific 
Edge developed and commercialised its CxBladder 
cancer test and we have been receiving revenue from 
the sales since 2015. The other two companies have not 
commercialised their diagnostic products as yet. 
Pacific Edge, a listed diagnostic company based in New 
Zealand, licensed midkine (MK) in 2010 for the use in its 
tests for the diagnosis, prognosis and disease management 
of bladder cancer. The Company received a total revenue 
of $1,221,0448 to date from the Pacific Edge license. This 
doesn’t include the royalty payment for the six months 
ending 31 March 2017, which was received after the 
closing of the 2017 financial year.
Pacific Edge announced the achievement of a number of 
material milestones during reporting period, some of these 
are listed below. They have also reported a 62% increase 
in operating revenue to $8.1 million for the 2017 financial 
year (ended on 31 March 2017). 
•  In October 2016 Pacific Edge became Approved Provider 
to Tricare Health Plan Networks in the US, which provides 
health care to 9.4 million beneficiaries of the US Military 
Health system. 
•  In October 2016 CxBladder® Monitor was adopted 
as a replacement for cystoscopy for low risk patients 
monitored for recurrence of bladder cancer by the 
Waitemata District Health Board. 
•  In December 2016 clinical study results of CxBladder® 
Monitor were accepted for publication in the American 
Journal of Urology. The study confirmed strong 
performance (93% sensitivity and 97% negative 
predictive value) of the test and the potential of it to 
replace cystoscopy in low risk patients.
Pacific Edge, in their most recent Annual Report, 
foreshadowed increase in CxBladder® sales as the utility 
and application of the test continues to broaded.
KINERA LIMITED –  
MK MANUFACTURE SUPPORTING 
PRE-IND WORK
Kinera has a broad patent portfolio using MK protein for 
the treatment of ischemic conditions including heart attack 
and stroke, and covering the manufacturing process for 
MK using Pichia pastoris. Extensive pre-clinical evidence 
has been unequivocal in demonstrating the benefit of 
single or chronic MK dosing in improving mortality and 
cardiac output following heart attack in animal models or 
this disease.  
Coronary heart disease remains the biggest cause of 
mortality world-wide and, whilst mortality rates have been 
improving, there is an urgent need for better management 
of myocardial infarct in those surviving an acute event. 
Minimising damage to heart muscle during ischemia and 
from the subsequent injury following restoration of blood 
flow is not addressed by current medications.