Collaboration to introduce nanotechnologies in early stage drug development

Fármacos complejos no biológicos/ Novedades | Posted 26/08/2016 post-comment0 Post your comment

The Frederick National Laboratory for Cancer Research (Frederick National Lab) announced on 10 June 2016 that it was collaborating with several major pharmaceutical companies. The collaboration aims to help them adopt nanotechnologies in early stage drug development, which, says the lab, is when the approach is most efficient and cost-effective.

Nanoparticle V13J18

Nanomedicine is a term which can be used to define the application of nanotechnology in medicine. It deals with particles in the size range of 100 nanometres (nm) or less. Nanomedicines include liposomes, polymer congugates, protein/antibody conjugates, block polymer micelles, cross-linked (nano)gels, bioactive synthetic polymers/vesicles, nanoparticles and nano-sized drug crystals. These nanomedicines are mainly anticancer, anti-infective or immunomodulator drugs [1].

The Frederick National Lab is a federal national laboratory sponsored by the National Cancer Institute, which is part of the US National Institutes of Health.

The Lab’s Nanotechnology Characterization Laboratory (NCL) has already been working with companies for some time in order to help reformulate cancer drugs that have failed in human clinical trials because of toxicity or other issues. But now the lab is working with pharma giants Amgen, AstraZeneca and Pfizer on nanotechnology formulations to improve candidate cancer drugs early on, before they are used in first-in-human studies.

Applying smart drug formulations early in the pipeline it is hoped ‘will increase the chance of success for these drugs’, according to Dr Stephen Stern, Senior Principal Scientist at NCL.

‘The pharmaceutical industry has begun to recognize the benefits of nanotechnology in developing cancer drugs because nanoformulations can target drugs to tumour sites without harming the rest of the body, and thus reduce or eliminate side effects’, according to Dr Jennifer Grossman, another scientist at NCL.

Since it began in 2004, NCL has characterized more than 350 nanoparticles for medical applications, helped set industry standards for nanoparticle characterization and collaborated in advancing 10 nanomedicines into human clinical trials.

The collaborations with the three companies will focus on formulating pharmaceuticals for delivery to solid tumours and producing nano-formulations of a compound to enhance its ability to disperse throughout a tumour.

Nanomedicines are often mentioned in the context of non-biological complex drugs (NBCDs). The European Medicines Agency (EMA) has recognized the complications associated with approval of originator NBCDs and has in the past therefore requested extra information to support follow-on NBCDs on a case-by-case basis.

Related articles
EU guidelines for follow-on NBCDs

Regulations for follow-on NBCDs

1. GaBI Online - Generics and Biosimilars Initiative. The future of nanomedicines - nanosimilars []. Mol, Belgium: Pro Pharma Communications International; [cited 2016 Aug 26]. Available from:

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2016 Pro Pharma Communications International. All Rights Reserved.

Source: Frederick National Lab

comment icon Comments (0)
Post your comment
Most viewed articles
Sobre GaBI
INICIO/Sobre GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
INICIO/Directrices Posted 08/10/2010