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Optimal design and analysis of clinical trials

9. November 2017 @ 14:00 - 18:00

November 9, 2017 at 14:00 – 16:00
Benzon Auditorium,
University of Copenhagen
Universitetsparken 2, 2100 København Ø

Careful planning of the clinical trial design is pertinent in obtaining the best estimation of the dose-response or exposure-response relationships. Thus, issues in trial conduct such as design, dose-selection, sample size allocations and analyses should be thoughtfully addressed during trial design in order to get the best precision of parameter estimates. The current meeting will give an overview on optimal design opportunities and challenges and present two examples of estimation of exposure-response relationships in clinical trials and the impact of different trial designs.

Program:

14:00 – 14:05
Welcome
Trine Meldgaard Lund, University of Copenhagen, Denmark

14:05 – 14:30
Estimation of the exposure-response relationship in phase 2 clinical trials for drug combinations
Theodoros Papathanasiou, University of Copenhagen and Novo Nordisk, Denmark

14:30 – 14:55
Estimation of the exposure-response relationship in clinical trials of haemophilia: a comparison of trial designs
Malte Selch Larsen, University of Copenhagen and Novo Nordisk, Denmark

14:55 – 15:15
Coffee, fruit and cake

15.15 – 16.00
Optimal design: opportunities and challenges
Andrew Hooker, Uppsala University, Sweden

Details

Date:
9. November 2017
Time:
14:00 - 18:00
Event Category:

Organizer

Danish Pharmaceutical Society

Venue

Københavns Universitet
Nørregade 10
København K, 1165 Danmark
+ Google Map

Details

Date:
9. November 2017
Time:
14:00 - 18:00
Event Category:

Organizer

Danish Pharmaceutical Society

Venue

Københavns Universitet
Nørregade 10
København K, 1165 Danmark
+ Google Map