Immupharma PLC CANCER UPDATE: IPP-204106 (6464E)
February 11 2015 - 7:03AM
UK Regulatory
TIDMIMM
RNS Number : 6464E
Immupharma PLC
11 February 2015
FOR IMMEDIATE RELEASE 11 FEBRUARY 2015
CANCER UPDATE: IPP-204106
ImmuPharma PLC (LSE:IMM), ("ImmuPharma" or the "Company"), the
specialist drug discovery and development company, provides an
update on its lead Cancer programme - IPP-204106.
As previously stated, the Phase I/IIa clinical trial with the
next generation "polyplexed Nucant" formulation taking place in
three European hospitals including the prestigious Institute Jules
Bordet in Belgium, has been completed.
This Phase I/IIa study was a dose-finding adaptive study where
the Nucant was associated with chondroitin sulfate, which has shown
in preclinical studies a strong potentiating effect of the Nucant.
The results demonstrate that the maximum tolerated dose with
chondroitin sulfate was 9mg/kg. This was the primary objective of
the study.
In preclinical studies it was indicated that a 1mg/kg equivalent
human dose with chondroitin sulfate in a combination therapy using
the cancer drug Gemcitabin demonstrated a massive reduction in
tumour volume in mouse pancreatic cancer.
These Phase I/IIa results now allow ImmuPharma, from a
regulatory perspective, to commence a Phase II study in pancreatic
cancer using the optimum human dosage.
A further update on this new Phase II study will be given in due
course.
-Ends-
For further information please contact:
+ 44 (0) 20 7152
ImmuPharma plc 4080
Dimitri Dimitriou, Chief
Executive Officer
Dr Robert Zimmer, President
and Chief Scientific Officer
Richard Warr, Chairman
Lisa Baderoon, Head of Investor
Relations + 44 (0) 7721 413496
Panmure, Gordon & Co., NOMAD
& Broker +44 (0) 20 7886 2500
Hugh Morgan, Fred Walsh,
Duncan Monteith
This information is provided by RNS
The company news service from the London Stock Exchange
END
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