Drug Delivery for Clinical Trials

Course aim

To provide an understanding of the procedures required for discovering and designing, developing and testing novel drugs, and the use of novel drugs in clinical trials.

Course content

Overview the procedures and processes involved in drug design and development for clinical trials; disease states and the need for treatments; history of drug discovery; identification of drug targets through disease research (including pathophysiology and molecular pathways of damage); developing compounds to act on a target; current targets and therapies in development; regulated manufacturing of compounds; high-throughput screening; pre-clinical studies; research ethics (animal and human); moving from pre-clinical to clinical trials and approvals required; study flaws and level of evidence; importance of study design; and clinical trial management.

Textbook(s)

Nil

Prerequisite(s)

Corequisite(s)

Nil

Teaching method

Note: These components may or may not be scheduled in every study period. Please refer to the timetable for further details.

Assessment

Portfolio, Presentation, Quiz

Fees

EFTSL*: 0.125
Commonwealth Supported program (Band 2)
To determine the fee for this course as part of a Commonwealth Supported program, go to:
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Fee-paying program for domestic and international students
International students and students undertaking this course as part of a postgraduate fee paying program must refer to the relevant program home page to determine the cost for undertaking this course.

Non-award enrolment
Non-award tuition fees are set by the university. To determine the cost of this course, go to:
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Not all courses are available on all of the above bases, and students must check to ensure that they are permitted to enrol in a particular course.

* Equivalent Full Time Study Load. Please note: all EFTSL values are published and calculated at ten decimal places. Values are displayed to three decimal places for ease of interpretation.