Drug Discovery

Course content

The following topics will be covered in lectures during the course:

  • Target classes: receptors, channels, transporters and enzymes
  • Target identification and evaluation
  • Target validation using genetic technologies
  • Drug discovery aspects related to drug development aspects
  • Drug design aspects related to biopharmaceuticals and small molecules
  • Translational aspects ranging from a molecular target to whole animals
  • Case stories

 

Target prioritization, potential pitfalls and literature search will be covered in workshops.

Education

Master's Programme in Industrial Drug Development - compulsory

 

See homepage for course dates

Compulsory for Master of Industrial Drug Development (MIND) students, elective for other part-time master's students at the Faculty of Health and Medical Sciences (subject to study board approval) and open for freelance students who meet the admission criteria.

The course is intended for drug discovery and development professionals, who would like to advance their knowledge in modern technologies and approaches used in target identification/​validation, drug discovery and lead optimisation.

Learning outcome

The overall objective of the course is to provide the student with a general comprehension of the elements involved in modern drug discovery. The course will therefore cover a mix of general topics, as well as specific example cases.

The majority of drug discovery programs are directed towards design of either biopharmaceuticals or small molecules acting selectively at specific targets. As an initial step, the target involved in a given disease has to be identified and validated. Subsequently, ligands designed and optimized to act selectively at the target are identified. During this lead optimization process a number of considerations, such as ADME, toxicology and production, have to be taken into consideration. Finally, the lead candidates have to show efficacy in relevant animal disease models before the final candidate can enter pre-clinical studies. In the this course, we will focus on the target identification and validation as well as drug discovery and lead optimization processes.

Upon completion of the course, participants are expected to be able to:

Knowledge

  • Demonstrate comprehension of target identification and validation methods and processes
  • Demonstrate insight into lead optimization methods and processes


Skills

  • Ability to select important parameters for lead optimization and lead candidate progression
  • Orally present a subject in the drug discovery area (however, this is not part of the assessment)


Competencies

  • Conduct a valid scientific literature study in the area of drug discovery
  • Write a scientifically-based report on drug discovery aspects using scientific literature

The course is organized as an intensive 5-day course and will comprise approximately 15 lectures, 3 afternoon workshops, an afternoon with student presentations and a symposium.
Note: The exam will require students to set aside time after the course dates.

Recommended reading for the lectures:

“Drug Discovery and Development” by Humphrey P. Rang and Duncan Richards (Elsevier, 3rd Ed, 2022, ISBN 978-0-7020-7804-0)

The below chapters are ‘need to know’ before the lectures as they form the basis of the course, including lectures and workshops:

Section 1: Introduction and background:

Chapter 2: The nature of disease and the purpose of therapy

Chapter 3: Therapeutic modalities

Section 2: Drug Discovery:

Chapter 4: Target selection

Chapter 5: From drug target to drug discovery

The following chapters are ‘nice to know’ before the lectures. They will increase your basic knowledge of the subject and thus increase your outcome of the lecture:

Section 2: Drug Discovery:

Chapters 6 to 13

Workshops

All workshop notes and materials are ‘need to know’.

Examination

The examination report will be based on a literature search performed by the participants and there is therefore no common syllabus for the course. Selected reviews may be provided by the organizers prior to the course as an introduction to the examination topic.

Applicants must meet the following criteria:
• A bachelor's degree, a professional bachelor’s degree, a diploma degree, a master’s degree or equivalent within chemistry, biochemistry, pharmacy, medicine, biomedicine, human biology, molecular biology, veterinary sciences, health sciences, nursing, engineering or equivalent.
• At least two years of relevant work experience related to development of medicines
• Proficiency in English

Oral
Peer feedback (Students give each other feedback)
ECTS
3 ECTS
Type of assessment
Written assignment
Type of assessment details
The individual written assignment is based on an example case. The assignment must be based on original peer-reviewed scientific articles found by literature search performed by the participants and there is therefore no common syllabus for the course. The participants will be introduced to literature searches during the course and the examination assignment is typically based on 20-40 articles.
Marking scale
7-point grading scale
Censorship form
External censorship
Exam period

Deadline for submission of written report to be announced on the MIND homepage.

Re-exam

The exam form for the reexam is the same as the ordinary exam. See dates in the exam schedule on the MIND homepage.

Criteria for exam assessment

To achieve the grade 12 the student should be able to:

Knowledge:

  • Demonstrate comprehension of target identification and validation methods and processes
  • Demonstrate insight into lead optimization methods and processes

 

Skills

  • Apply basic computational methods in the area of bioinformatics and literature serach
  • Ability to select important parameters for lead optimization and lead candidate progression

 

Competencies

  • Conduct a valid scientific literature study in the area of drug discovery
  • Write a scientifically based report on drug discovery aspects using scientific literature

Part time Master and Diploma courses

  • Category
  • Hours
  • Lectures
  • 24
  • Preparation
  • 18
  • Theory exercises
  • 18
  • Exam
  • 22
  • English
  • 82

Kursusinformation

Language
English
Course number
SMIMM1131U
ECTS
3 ECTS
Programme level
Part Time Master
Duration
5 days. Note: The exam will require students to set aside time after the course dates.
Placement
Spring
Price

Fees are published on the programme's homepage at  https://mind.ku.dk/tuition/ Fee includes course materials and lunch/coffee. Prices may be subject to change.

Textbooks must be purchased by the participants.

Schedulegroup
See course calendar
Capacity
25 participants
Studyboard
Study Board for the Professionel Master´s Degree Programmes at The Faculty og Health and Medical Science
Contracting department
  • Department of Drug Design and Pharmacology
Contracting faculty
  • Faculty of Health and Medical Sciences
Course Coordinator
  • Stephan Pless   (13-7d7e6f7a726b78387a766f7d7d4a7d7f786e38757f386e75)
Teacher

Lecturers will be leading experts from both industry and academia (the names below are a list of previous lecturers on this course). Note that lecturers will be selected based on course composition, attendee numbers and availability.

Philipp Jaeger, Boehringer Ingelheim
Lotte Bjerre Knudsen, Novo Nordisk
Cord Brakebusch, BRIC/University of Copenhagen
David Hackos, Genentech
Sebastian Meyer, Numab
Benny Bang-Andersen, Lundbeck A/S
Torben Hansen, University of Copenhagen
Kristian Strømgaard, University of Copenhagen
Morten Grunnet, Lundbeck A/S
Petrine Wellendorph, Ceremedy
Thomas Høeg-Jensen, Novo Nordisk

Saved on the 24-04-2024

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