Dr Tahlia Meola
Research Fellow: Clinical Trials
School of Pharmacy and Biomedical Science
College of Health
Dr Tahlia Meola is an early career pharmaceutical scientist within the Clinical Pharmacology and Therapeutics Research Group at the University of South Australia. Her doctoral work focussed on developing innovative pharmaceutical formulations to overcome the challenges associated with the oral delivery of drugs, specifically to improve drug absorption to enable easier dosing regimens and improve patient compliance. Tahlia’s current research partners with pharmaceutical industry to explore rationale dosing regimens to optimise medicine use. Tahlia has extensive experience in early phase clinical trial conduct in accordance with regulatory standards, managing all aspects from study design to clinical trial reporting.
| Date | Position | Institution name |
|---|---|---|
| 2023 - ongoing | Research Fellow | University of South Australia |
| Date | Institution name | Country | Title |
|---|---|---|---|
| 2017 - 2022 | University of South Australia | Australia | Doctor of Philosophy |
| 2016 - 2017 | University of South Australia | Australia | Bachelor of Biomedical Research (Honours) |
| 2013 - 2015 | University of South Australia | Australia | Bachelor of Pharmaceutical Science |
| Year | Citation |
|---|---|
| 2020 | Joyce, P., Schultz, H. B., Meola, T. R., & Prestidge, C. A. (2020). Polymer lipid hybrid (PLH) formulations: A synergistic approach to oral delivery of challenging therapeutics. A synergistic approach to oral delivery of challenging therapeutics. In Delivery of Drugs Volume 2 Expectations and Realities of Multifunctional Drug Delivery Systems (pp. 1-27). Elsevier. DOI Scopus5 |
| 2020 | Joyce, P., Schultz, H. B., Meola, T. R., & Prestidge, C. A. (2020). Polymer lipid hybrid (PLH) formulations: a synergistic approach to oral delivery of challenging therapeutics. In R. Shegokar (Ed.), Source details - Title: Delivery of Drugs. Volume 2: Expectations and Realities of Multifunctional Drug Delivery Systems (pp. 1-27). UK: Elsevier. DOI |
| Year | Citation |
|---|---|
| 2024 | Brungs, D., Hill, J., Aghmesheh, M., Ackland, S. P., Parker, S., Jokela, R. M., . . . Clingan, P. R. (2024). A phase I dose-escalation study of an all-in-one 5-fluorouracil and leucovorin co-formulation administered after failure of standard treatment. In Journal of Clinical Oncology Vol. 42 (pp. 1 page). IL, Chicago: LIPPINCOTT WILLIAMS & WILKINS. DOI |
Courses I teach
- PHAR 2024 Clinical Trials for Drug Development (2024)