SYDNEY, AUSTRALIA--(Marketwired - Dec 19, 2016) -
- Competent Authority and Ethics Committee approval received in the United Kingdom for AIPAC
- Recruitment of patients in second cohort of AIPAC study completed
- Interim data for AIPAC and TACTI-mel trials of IMP321 due in December 2016
Prima BioMed Ltd (
AIPAC (Active Immunotherapy PAClitaxel) is a multi-national, randomised, double-blind, placebo-controlled study of IMP321-plus-paclitaxel in metastatic breast cancer. The safety run-in phase of the first cohort of 15 patients is being conducted across 11 clinical sites in Belgium, The Netherlands and Hungary. Recruitment of the last two patients in this cohort was completed in October. The first safety and pharmacokinetic data from these 15 patients is expected in late December 2016. As previously announced, AIPAC's expected duration based on forecast recruitment times and patient follow up is approximately three years.
Prima also confirms that interim data from the first cohort of patients in its Phase I, TACTI-mel clinical trial of IMP321 together with KEYTRUDA® for metastatic melanoma patients is also expected in late December 2016.
About Prima BioMed
Prima BioMed is listed on the Australian Securities Exchange, and on the NASDAQ in the US. For further information please visit www.primabiomed.com.au.
For further information please contact:
U.S. Investors:
Mr Matthew Beck
The Trout Group LLC
+1 (646) 378-2933
mbeck@troutgroup.com
Australia Investor/Media:
Mr Matthew Gregorowski
Citadel Communications
+61 (0) 422 534 755
mgregorowski@citadelpr.com.au