PCI Biotech: First patient treated in the phase I/II extension study of Amphinex


Oslo, 22 February 2012 - PCI Biotech (PCIB) the Norwegian biopharmaceutical company, reported today that the first patient has been treated in the phase I/II extension study of Amphinex in combination with the cytotoxic agent bleomycin. The objective of the study is to investigate doses below the levels used in the phase I/II study that was completed in 2011. The extension study will be performed at University College Hospital (UCH) in London, and will include up to 9 patients.


About PCI Biotech
PCI Biotech is a Norwegian biopharmaceutical company developing a novel light directed drug delivery system based on its patented photochemical internalisation (PCI) technology. Originating from world leading research at the Norwegian Radium Hospital, the PCI method involves first injecting Amphinex® and thereafter the therapeutic drug to be specifically delivered to the diseased cells. When these are illuminated the cells' endosomes are ruptured to allow successful intracellular delivery of the drug.

PCI can enhance the delivery of all molecules taken into the cell by endocytosis. This includes most types of macromolecules, drugs carried by antibodies or nanoparticles, as well as some small molecule drugs.

PCI Biotech follows a dual strategy of using its technology to improve the effect both of existing drugs and for emerging treatments such as gene therapy. PCI Biotech's first clinical study combines the proven photosensitiser Amphinex® with the cytotoxic agent bleomycin. Other studies are planned for the delivery of other cancer drugs in relevant indications.

For more information visit: www.pcibiotech.com

Contact information:
PCI Biotech Holding ASA, Strandveien 55, N-1366 Lysaker
Per Walday, CEO, pw@pcibiotech.no, Mobile: +47 917 93 429
Bernt-Olav Røttingsnes, CFO, bor@pcibiotech.no, Mobile: +47 913 47 021



This information is subject of the disclosure requirements pursuant to section 5-12 of the Norwegian Securities Trading Act.
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