SwePub
Tyck till om SwePub Sök här!
Sök i LIBRIS databas

  Utökad sökning

onr:"swepub:oai:DiVA.org:uu-133104"
 

Sökning: onr:"swepub:oai:DiVA.org:uu-133104" > Benefits of Pharmac...

Benefits of Pharmacometric Model-Based Design and Analysis of Clinical Trials

Karlsson, Kristin E, 1975- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Farmakometri
Jonsson, E Niclas (preses)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Karlsson, Mats O (preses)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
visa fler...
Grahnén, Anders (preses)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Smith, Michael K (opponent)
Pfizer Global Research and Development, Sandwich, UK
visa färre...
 (creator_code:org_t)
Uppsala : Acta Universitatis Upsaliensis, 2010
Engelska 71 s.
Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Pharmacy, 1651-6192 ; 133
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • Quantitative pharmacokinetic-pharmacodynamic and disease progression models are the core of the science of pharmacometrics which has been identified as one of the strategies that can make drug development more effective. To adequately develop and utilize these models one needs to carefully consider the nature of the data, choice of appropriate estimation methods, model evaluation strategies, and, most importantly, the intended use of the model. The general aim of this thesis was to investigate how the use of pharmacometric models can improve the design and analysis of clinical trials within drug development. The development of pharmacometric models for clinical assessment scales in stroke and graded severity events, in this thesis, show the benefit of describing data as close to its true nature as possible, as it increases the predictive abilities and allows for mechanistic interpretations of the models. Performance of three estimation methods implemented in the mixed-effects modeling software NONMEM; 1) Laplace, 2) SAEM, and 3) Importance sampling, applied when modeling repeated time-to-event data, was investigated. The two latter methods are to be preferred if less than approximately half of the individuals experience events. In addition, predictive performance of two validation procedures, internal and external validation, was explored, with internal validation being preferred in most cases. Model-based analysis was compared to conventional methods by the use of clinical trial simulations and the power to detect a drug effect was improved with a pharmacometric design and analysis. Throughout this thesis several examples have shown the possibility of significantly reducing sample sizes in clinical trials with a pharmacometric model-based analysis. This approach will reduce time and costs spent in the development of new drug therapies, but foremost reduce the number of healthy volunteers and patients exposed to experimental drugs.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

model-based analysis
pharmacometrics
modeling
disease progression
NONMEM
SAEM
Importance sampling
repeated time-to-event
RTTCE
RCEpT
NIH stroke scale
Barthel index
internal validation
external validation
study power
study design
PHARMACY
FARMACI
Pharmacokinetics and Drug Therapy
Farmakokinetik och läkemedelsterapi

Publikations- och innehållstyp

vet (ämneskategori)
dok (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy