
Overview
Background
David is a passionate and driven scientist with a successful track record in translational commercially focused technical and academic leadership. David has worked in academia and industry at the interface of chemistry, biochemistry and biology. He has successfully designed and developed several oncology nanomedicines and driven them forward into clinical trials.
As Director of the Protein Expression Facility (PEF) within The University of Queensland, David and his team strive to build collaborations and provide excellent service provision with a wide variety of researchers across academia and industry. Through this work we ensure PEF achieves its vision to be a world leader in protein research services and innovative solutions for protein production driving scientific success.
Availability
- Professor David Owen is:
- Available for supervision
Qualifications
- Bachelor (Honours), The University of Queensland
- Doctor of Philosophy, Australian National University
Research interests
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Protein Science
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Nanotechnology
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Radiotheranostics
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Cancer Biology
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Bioconjugation
Research impacts
As VP Research at Starpharma I lead the team that discovered and developed a deep pipeline of dendrimer-drug conjugates for human health, as well as applications of dendrimers in industrial and agrochemical applications. During this time I was the lead scientist involved in the discovery and development of the DEP® platform with 4 candidates that transitioned into clinical trials;
1. DEP® docetaxel: Phase 2 clinical trials as both a monotherapy and combination with gemcitabine in patients with lung, pancreatic, oesophageal, cholangiocarcinoma and gastric cancers.
2. DEP® cabazitaxel: Phase 2 clinical trials as a monotherapy against prostate, as well as advanced ovarian, gastro-oesophageal, cholangiocarcinoma, and head and neck cancers.
3. DEP® irinotecan:” Phase 2 clinical trial as a monotherapy and combination on patients with platinum resistant ovarian cancer, as well as colorectal, breast, pancreatic, lung, and oesophageal cancers.
4. AZD0466: Licensed to AstraZeneca is in a Global Phase 1/2 clinical trial in patients with advanced relapsed/refractory leukemia (NCT04865419), withdrawn July 2023.
I have a strong record in building national and international research collaborations; working with multiple pharmaceutical companies e.g. AstraZeneca, Genentech, Merck, GSK, Eli Lilly, ChaseSun and others (generating >$9 M in external R&D revenue), as well as strong collaborations with academic groups e.g. Prof Christopher Porter from Monash University; Prof Kristopher Thurecht from the University of Queensland; and the late Prof Carleen Cullinane from the Peter MacCallum Cancer [generated > $2.6 M in research support from schemes such as; ARC Linkage, Cancer Australia, the Science and Industry Endowment Fund (SIEF). More recently with the ARC’s Industrial Transformation Research Hub].
Over my career, I have mentored and supervised 10 postdoctoral fellows, >36 PhD level scientists and co-supervised 1 PhD student to completion. Several of these scientists have moved on to senior leadership roles in industry. I have held advisory roles in the ARC Centre of Excellence in CBNS (Nov 2014 – Dec 2020) and the Pharmaceutical Science Advisory and Stakeholders Group, Monash University (2014 – 2019). I have 48 published works; 1,647 citations, h-index = 23 (Scopus/SciVal, 2023), I am listed as an inventor on 4 granted patents and 18 patent applications.
Works
Search Professor David Owen’s works on UQ eSpace
2011
Journal Article
Characterisation and tumour targeting of PEGylated polylysine dendrimers bearing doxorubicin via a pH labile linker
Kaminskas, Lisa M., Kelly, Brian D., McLeod, Victoria M., Sberna, Gian, Owen, David J., Boyd, Ben J. and Porter, Christopher J. H. (2011). Characterisation and tumour targeting of PEGylated polylysine dendrimers bearing doxorubicin via a pH labile linker. Journal of Controlled Release, 152 (2), 241-248. doi: 10.1016/j.jconrel.2011.02.005
2011
Journal Article
Capping methotrexate α-carboxyl groups enhances systemic exposure and retains the cytotoxicity of drug conjugated pegylated polylysine dendrimers
Kaminskas, Lisa M., Kelly, Brian D., McLeod, Victoria M., Sberna, Gian, Boyd, Ben J., Owen, David J. and Porter, Christopher J. H. (2011). Capping methotrexate α-carboxyl groups enhances systemic exposure and retains the cytotoxicity of drug conjugated pegylated polylysine dendrimers. Molecular Pharmaceutics, 8 (2), 338-349. doi: 10.1021/mp1001872
2010
Journal Article
Dendrimers enhance delivery of small molecule and biological drugs: Control solubility, half-life, toxicity and targeting
Owen, David and Barrett, Paul (2010). Dendrimers enhance delivery of small molecule and biological drugs: Control solubility, half-life, toxicity and targeting. ONdrugDelivery (4), 21-24.
2010
Journal Article
Enantioselective inhibition of squalene synthase by aziridine analogues of presqualene diphosphate
Koohang, Ali, Bailey, Jessica L., Coates, Robert M., Erickson, Hans K., Owen, David and Poulter, C. Dale (2010). Enantioselective inhibition of squalene synthase by aziridine analogues of presqualene diphosphate. Journal of Organic Chemistry, 75 (14), 4769-4777. doi: 10.1021/jo100718z
2009
Journal Article
Total Synthesis of the Potent Anticancer Aglaia Metabolites (-)-Silvestrol and (-)-Episilvestrol and the Active Analogue (-)-4-Desmethoxyepisilvestrol
Adams, Tim E., Sous, Mariana El, Hawkins, Bill C., Hirner, Sebastian, Holloway, Georgina, Khoo, Mui Ling, Owen, David J., Paul Savage, G., Seammells, Peter J. and Rizzacasa, Mark A. (2009). Total Synthesis of the Potent Anticancer Aglaia Metabolites (-)-Silvestrol and (-)-Episilvestrol and the Active Analogue (-)-4-Desmethoxyepisilvestrol. Journal of the American Chemical Society, 131 (4), 1607-1616. doi: 10.1021/ja808402e
2007
Journal Article
Total synthesis of (-)-episilvestrol and (-)-silvestrol
El Sous, Mariana, Khoo, Mui Ling, Holloway, Georgina, Owen, David, Scammells, Peter J. and Rizzacasa, Mark A. (2007). Total synthesis of (-)-episilvestrol and (-)-silvestrol. Angewandte Chemie - International Edition, 46 (41), 7835-7838. doi: 10.1002/anie.200702700
2007
Journal Article
Synthesis and biological evaluation of galactofuranosyl alkyl thioglycosides as inhibitors of mycobacteria
Davis, Chris B., Hartnell, Regan D., Madge, Paul D., Owen, David J., Thomson, Robin J., Chong, Andrew K.J., Coppel, Ross L. and Von Itzstein, Mark (2007). Synthesis and biological evaluation of galactofuranosyl alkyl thioglycosides as inhibitors of mycobacteria. Carbohydrate Research, 342 (12-13), 1773-1780. doi: 10.1016/j.carres.2007.04.027
2007
Journal Article
Synthesis and evaluation of galactofuranosyl N,N-dialkyl sulfenamides and sulfonamides as antimycobacterial agents
Owen, David J., Davis, Chris B., Hartnell, Regan D., Madge, Paul D., Thomson, Robin J., Chong, Andrew K.J., Coppel, Ross L. and Von Itzstein, Mark (2007). Synthesis and evaluation of galactofuranosyl N,N-dialkyl sulfenamides and sulfonamides as antimycobacterial agents. Bioorganic and Medicinal Chemistry Letters, 17 (8), 2274-2277. doi: 10.1016/j.bmcl.2007.01.068
2003
Journal Article
Efficient syntheses of benzothiazepines as antagonists for the mitochondrial sodium-calcium exchanger: Potential therapeutics for type II diabetes
Pei, Yazhong, Lilly, Michael J., Owen, David J., D'Souza, Lawrence J., Tang, Xiao-Qing, Yu, Jinghua, Nazarbaghi, Ramina, Hunter, Andrew, Anderson, Christen M., Glasco, Susan, Ede, Nicholas J., James, Ian W., Maitra, Uday, Chandrasekaran, S., Moos, Walter H. and Ghosh, Soumitra S. (2003). Efficient syntheses of benzothiazepines as antagonists for the mitochondrial sodium-calcium exchanger: Potential therapeutics for type II diabetes. Journal of Organic Chemistry, 68 (1), 92-103. doi: 10.1021/jo020446t
2002
Journal Article
A convenient synthesis of C-galactofuranosylic compounds (C-galactofuranosides)
Owen, David J., Thomson, Robin J. and Von Itzstein, Mark (2002). A convenient synthesis of C-galactofuranosylic compounds (C-galactofuranosides). Carbohydrate Research, 337 (21-23), 2017-2022. doi: 10.1016/S0008-6215(02)00133-7
2001
Journal Article
Synthesis of Functional <i>Ras</i> Lipoproteins and Fluorescent Derivatives
Kuhn, Karsten, Owen, David J., Bader, Benjamin, Wittinghofer, Alfred, Kuhlmann, Jürgen and Waldmann, Herbert (2001). Synthesis of Functional Ras Lipoproteins and Fluorescent Derivatives. Journal of the American Chemical Society, 123 (6), 1023-1035. doi: 10.1021/ja002723o
2000
Journal Article
Identification of endogenous gibberellins in strawberry, including the novel gibberellins GA123, GA124 and GA125
Blake, Patrick S, Taylor, David R, Crisp, Carol M, Mander, Lewis N and Owen, David J (2000). Identification of endogenous gibberellins in strawberry, including the novel gibberellins GA123, GA124 and GA125. Phytochemistry, 55 (8), 887-890. doi: 10.1016/S0031-9422(00)00237-5
2000
Journal Article
Phosphoisoprenoid binding specificity of geranylgeranyltransferase type II
Thoma N.H., Iakovenko A., Owen D., Scheidig A.S., Waldmann H., Goody R.S. and Alexandrov K. (2000). Phosphoisoprenoid binding specificity of geranylgeranyltransferase type II. Biochemistry, 39 (39), 12043-12052. doi: 10.1021/bi000835m
2000
Journal Article
A one-pot synthesis of novel N,N-dialkyl-S-glycosylsulfenamides
Owen, David J. and Von Itzstein, Mark (2000). A one-pot synthesis of novel N,N-dialkyl-S-glycosylsulfenamides. Carbohydrate Research, 328 (3), 287-292. doi: 10.1016/S0008-6215(00)00110-5
2000
Journal Article
Bioorganic synthesis of lipid-modified proteins for the study of signal transduction
Bader, Benjamin, Kuhn, Karsten, Owen, David J., Waldmann, Herbert, Wittinghofer, Alfred and Kuhlmann, Jürgen (2000). Bioorganic synthesis of lipid-modified proteins for the study of signal transduction. Nature, 403 (6766), 223-226. doi: 10.1038/35003249
1999
Journal Article
Peptide conjugates as tools for the study of biological signal transduction
Eisele, Frank, Owen, David J. and Waldmann, Herbert (1999). Peptide conjugates as tools for the study of biological signal transduction. Bioorganic and Medicinal Chemistry, 7 (2), 193-224. doi: 10.1016/S0968-0896(98)00204-1
1999
Journal Article
Synthesis and evaluation of aziridine analogues of presqualene diphosphate as squalene synthase inhibitors
Koohang, Ali, Coates, Robert M., Owen, David and Poulter, C. Dale (1999). Synthesis and evaluation of aziridine analogues of presqualene diphosphate as squalene synthase inhibitors. Journal of Organic Chemistry, 64 (1), 6-7. doi: 10.1021/jo981833z
1999
Journal Article
Chemo-enzymatic synthesis of fluorescent Rab 7 proteins: Tools to study vesicular trafficking in cells
Owen, DJ, Alexandrov, K, Rostkova, E, Scheidig, AJ, Goody, RS and Waldmann, H (1999). Chemo-enzymatic synthesis of fluorescent Rab 7 proteins: Tools to study vesicular trafficking in cells. Angewandte Chemie-International Edition, 38 (4), 509-512. doi: 10.1002/(SICI)1521-3773(19990215)38:43.3.CO;2-V
1998
Journal Article
Identification of GA113, GA114, GA115 and GA116 and further novel gibberellins in Raphanus sativus
Nakayama, Massyoshi, Nishijima, Takaaki, Koshioka, Masaji, Yamane, Hisakazu, Owen, David J. and Mander, Lewis N. (1998). Identification of GA113, GA114, GA115 and GA116 and further novel gibberellins in Raphanus sativus. Phytochemistry, 48 (4), 587-593. doi: 10.1016/s0031-9422(98)00035-1
1998
Journal Article
Synthesis and confirmation of structure for a new gibberellin, 2β- hydroxy-GA12 (GA110), from spinach and oil palm
Owen, David J., Mander, Lewis N., Storey, John M.D., Huntley, Rachael P., Gaskin, Paul, Lenton, John R., Gage, Douglas A. and Zeevaart, Jan A.D. (1998). Synthesis and confirmation of structure for a new gibberellin, 2β- hydroxy-GA12 (GA110), from spinach and oil palm. Phytochemistry, 47 (3), 331-337. doi: 10.1016/S0031-9422(97)00577-3
Supervision
Availability
- Professor David Owen is:
- Available for supervision
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Supervision history
Current supervision
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Doctor Philosophy
The Molecular Characterisation of Myeloperoxidase (MPO) and its role in autoimmunity
Principal Advisor
Other advisors: Professor Ranjeny Thomas, Professor Fiona Simpson, Dr Pie Huda
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Doctor Philosophy
Assessment of Nanomedicine Efficacy and Mechanism using Metabolic Spectroscopic Imaging.
Associate Advisor
Other advisors: Associate Professor Idriss Blakey
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Doctor Philosophy
mRNA therapies for liver disorders
Associate Advisor
Other advisors: Associate Professor Seth Cheetham
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Doctor Philosophy
Broad Spectrum Medical Countermeasure development for Organophosphate Compounds
Associate Advisor
Other advisors: Professor Linda Lua
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Doctor Philosophy
Development of a versatile targeted alpha therapy platform
Associate Advisor
Other advisors: Dr Nick Fletcher, Dr Pie Huda
Media
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