ACoP15 Posters
ACoP15
Posters
SxP reviewed the ACoP program and abstracts to select content of interest for SxP
Link to the ACoP15 program and abstracts
Monday Nov 11
- (M-004)
- MBMA Bridging Models as A Tool for Exploration of Clinical Endpoints in Unstudied Indications [MBMA]
- (M-027)
- Model-based meta-analysis of safety for monomethyl auristatin E-conjugated antibody drug conjugates in cancer patients [MBMA]
- (M-036)
- Pharmacometric-Pharmacoeconomic Modeling and Simulation in Atopic Dermatitis: Informing Early Drug Development Decisions for a Hypothetical New Therapeutic [Early development decision making]
- (M-051)
- The impact of misspecified covariate models on inclusion and omission bias when using FREM and FFEM [Statistical methodology]
- (M-061)
- A clinical trial simulator tool for a randomized delayed start trial in Parkinson’s disease [Tools]
- (M-091)
- Fully Bayesian Covariate Selection in Population Pharmacokinetics and Pharmacodynamics Models Using Regularized Horseshoe Priors [Bayesian statistics]
- (M-099)
- Advancing Drug Development in Relapsed and Refractory Multiple Myeloma (RRMM): Assessing the Safety and Efficacy Landscape Utilizing Model-Based Meta-Analysis [MBMA]
- (M-108)
- How should we leverage prior adult knowledge for pediatric PK analysis? - A case study comparing Pooled and Bayesian population PK approaches [Bayesian statistics]
- (M-135)
- A Bayesian disease progression model for Major Depressive Disorder [Bayesian statistics]
Tuesday Nov 12
- (T-016)
- Bridging the Gap: A Comprehensive Checklist for Hybrid Pharmacometrics-Machine Learning Model Building to Support Oncology Clinical Development [AI/ML]
- (T-024)
- A Bayesian Approach to Item Response Theory Modeling for Exposure-Response Relationships in Stan [Bayesian Statistics]
- (T-042)
- Use of Model-informed Drug Development and Natural History Data to Inform the Development of Iluzanebart in ALSP: A Neurological Rare Disease [MIDD]
- (T-056)
- A modified Bayesian information criterion (mBIC) with multiple testing correction for population pharmacokinetic model building [Statistical methodology]
- (T-057)
- Hybrid Population PK-Machine Learning Model Approach to Predict Infliximab Concentrations in Pediatric Patients with Crohn’s Disease [AI/ML]
- (T-075)
- Enhancing Parameter Estimation Process for Pharmacokinetic-Pharmacodynamic Models with Meta-heuristic Optimization Approaches [Statistical methodology]
- (T-078)
- A Bayesian Semi-Mechanistic Dose-Finding Design for Phase I Drug Combination Trials in Oncology [Bayesian statistics]
- (T-091)
- Fast Stepwise Selection Methods for Efficient Covariate Model Development in Population Data Analysis [Statistical methodology]
- (T-135)
- Potential Bias Evaluation of Conventional Exposure-Response Analysis Methods: A Small Molecule Cancer Drug Example [Statistical methodology]
Wednesdsay Nov 13
- (W-003)
- Leveraging Machine Learning and Real-World Data: Time-to-Event Analysis of COVID-19 Patients Using Electronic Health Records [AI/ML, RWD/RWE]
- (W-008)
- The reference corrected VPC (rcVPC) - An informative model diagnostic for assessing underlying exposure-response relationships [Tools]
- (W-032)
- Longitudinal Joint Modeling of Modified Mayo Score and Dropout in Patients with Moderate to Severely Active Ulcerative Colitis [Statistical Methodology]
- (W-045)
- Clinical Trial Simulation to Assess Sample Size and Power For Detecting Differences in Pharmacokinetic Exposure Metrics [Statistical Methodology]
- (W-055)
- Confounding Impact of Event-Driven Exposure Phenomenon on Summary Exposure Metrics in Time-to-Event Exposure Response Analyses [Statistical Methodology]
- (W-069)
- Exploring Appropriate Prior Distributions for Covariance Matrix Estimation in Bayesian Population Pharmacokinetic Analysis [Bayesian statistics]
- (W-084)
- Exploring the feasibility of using AI to identify patient characteristics predictive of histological endpoints in metabolic dysfunction associated steatohepatitis (MASH) [AI/ML]
- (W-099)
- Constructing a virtual control arm and evaluating operating characteristics using TGI metrics to support go/no-go decisions for single-arm Phase Ib/II combination studies [Virtual control arm]
- (W-114)
- Consideration of Study design aspects in the creation of virtual populations for organ impairment studies: One size may not fit all [Virtual control arm]
- (W-133)
- Losing the Forest: Causal Shapley Additive Explanations for Interpretation of Population-Pharmacokinetic models [Statistical Methodology]
- (W-141)
- Disease progression modeling of myositis from real-world data [RWD/RWE]