A Model‐Based Approach to Predict Longitudinal HbA1c, Using Early Phase Glucose Data From Type 2 Diabetes Mellitus Patients After Anti‐Diabetic Treatment. (22nd April 2013)
- Record Type:
- Journal Article
- Title:
- A Model‐Based Approach to Predict Longitudinal HbA1c, Using Early Phase Glucose Data From Type 2 Diabetes Mellitus Patients After Anti‐Diabetic Treatment. (22nd April 2013)
- Main Title:
- A Model‐Based Approach to Predict Longitudinal HbA1c, Using Early Phase Glucose Data From Type 2 Diabetes Mellitus Patients After Anti‐Diabetic Treatment
- Authors:
- Kjellsson, Maria C.
Cosson, Valérie F.
Mazer, Norman A.
Frey, Nicolas
Karlsson, Mats O. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="jcph86-sec-0001" sec-type="section"> <p>Predicting late phase outcomes from early‐phase findings can help inform decisions in drug development. If the measurements in early‐phase differ from those in late phase, forecasting is more challenging. In this paper, we present a model‐based approach for predicting glycosylated hemoglobin (HbA1c) in late phase using glucose and insulin concentrations from an early‐phase study, investigating an anti‐diabetic treatment. Two previously published models were used; an integrated glucose and insulin (IGI) model for meal tolerance tests and an integrated glucose‐red blood cell‐HbA1c (IGRH) model predicting the formation of HbA1c from the average glucose concentration (C<sub>g, av</sub>). Output from the IGI model was used as input to the IGRH model. Parameters of the IGI model and drug effects were estimated using data from a phase1 study in 59 diabetic patients receiving various doses of a glucokinase activator. C<sub>g, av</sub> values were simulated according to a Phase 2 study design and used in the IGRH model for predictions of HbA1c. The performance of the model‐based approach was assessed by comparing the predicted to the actual outcome of the Phase 2 study. We have shown that this approach well predicts the longitudinal HbA1c response in a 12‐week study using only information from a 1‐week study where glucose and insulin concentrations were measured.</p><abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="jcph86-sec-0001" sec-type="section"> <p>Predicting late phase outcomes from early‐phase findings can help inform decisions in drug development. If the measurements in early‐phase differ from those in late phase, forecasting is more challenging. In this paper, we present a model‐based approach for predicting glycosylated hemoglobin (HbA1c) in late phase using glucose and insulin concentrations from an early‐phase study, investigating an anti‐diabetic treatment. Two previously published models were used; an integrated glucose and insulin (IGI) model for meal tolerance tests and an integrated glucose‐red blood cell‐HbA1c (IGRH) model predicting the formation of HbA1c from the average glucose concentration (C<sub>g, av</sub>). Output from the IGI model was used as input to the IGRH model. Parameters of the IGI model and drug effects were estimated using data from a phase1 study in 59 diabetic patients receiving various doses of a glucokinase activator. C<sub>g, av</sub> values were simulated according to a Phase 2 study design and used in the IGRH model for predictions of HbA1c. The performance of the model‐based approach was assessed by comparing the predicted to the actual outcome of the Phase 2 study. We have shown that this approach well predicts the longitudinal HbA1c response in a 12‐week study using only information from a 1‐week study where glucose and insulin concentrations were measured.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of clinical pharmacology. Volume 53:Number 6(2013:Jun.)
- Journal:
- Journal of clinical pharmacology
- Issue:
- Volume 53:Number 6(2013:Jun.)
- Issue Display:
- Volume 53, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 53
- Issue:
- 6
- Issue Sort Value:
- 2013-0053-0006-0000
- Page Start:
- 589
- Page End:
- 600
- Publication Date:
- 2013-04-22
- Subjects:
- Pharmacology -- Periodicals
Pharmacology -- Periodicals
Pharmacology, Clinical -- Periodicals
615.1 - Journal URLs:
- http://jcp.sagepub.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4604 ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0091-2700;screen=info;ECOIP ↗ - DOI:
- 10.1002/jcph.86 ↗
- Languages:
- English
- ISSNs:
- 0091-2700
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4958.680000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3317.xml