Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
Reading , RG2 6UU
The aim of this meeting is to provide a relaxed environment for career young statisticians
where they can present and discuss various statistical topics and interact/network with other statisticians in similar positions to themselves. The PSI conference and similar events can be daunting for some attendees both in terms of who is in the audience and also in being happy that what they present is deemed new and original. For this one day meeting the audience will be peers with similar levels of experience and will include content of interest to career young statisticians. In addition to presentations from fellow statisticians there will be a soft skills workshop on explaining statistics to non‐statisticians and ample opportunity to connect with colleagues across the industry.
CLICK HERE TO VIEW THE FLYER
Registration Costs:
| PSI Members | £25 + VAT |
| Non-Members | £95 + VAT |
The agenda for the meeting can be found below:
| 9.30 -9.55 | Registration |
| 9.55 – 10.00 | Welcome and Introduction |
| 10.00 – 11.00 | One label with different interpretations…Statistical lead, what does it really mean? |
|
| Charlotte Eden and Lucie Tesarova, QuintilesIMS |
| 11.00 – 11.20 | Break |
| 11.20 – 11.50 | Exploring recent developments in the MAMS methodology for designing an adaptive trial |
|
| Julia Abery, University of Reading |
| 11.50 – 12.20 | Seamless Study Designs & Real-time Data Capture Using Electronic Devices |
|
| Rhian Jacob, Roche |
| 12.20 – 13.20 | Lunch |
| 13.20 – 14:20 | Training session: Explaining statistics to non-statisticians |
|
| James Matcham, AstraZeneca / PSI Training Committee |
| 14.20 – 14.40 | Break |
| 14.40 – 15.10 | Introduction to Pharmacokinetics |
|
| Laura Cope, Quanticate |
| 15.10 – 15.40 | AdePro – A new Perspective on Safety Profiles |
|
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG |
| 15.40 – 16.00 | Break |
| 16.00 – 16.30 | Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes |
|
| Nirav Ratia, GSK |
| 16.30 | Close |
One label with different interpretations…Statistical lead, what does it really mean?
| Charlotte Eden and Lucie Tesarova, QuintilesIMS | Exploring the role of the Statistical lead from different perspectives. Focusing on life in a CRO to experiences in Pharma with audience participation to discuss how we work on some key factors throughout the life of a study. |
Exploring recent developments in the MAMS methodology for designing an adaptive trial
| Julia Abery, University of Reading | Multi-arm adaptive trials allow several new drugs to be assessed simultaneously, potentially giving improved efficiency over conventionally designed trials. In such a trial, data accumulating during the study are utilised to inform decisions about how the remainder of the trial should be conducted. Several different methodological approaches have been developed for multi-arm adaptive trials and a number of studies have compared the performance of different subsets of these proposed methods. The comparisons have not, however, considered the so-called MAMS approach, since methodology for the latter did not incorporate strong control of the family-wise error rate (FWER). Recently, the MAMS approach has been extended such that strong control of the FWER can be guaranteed. Furthermore, an automated process has been developed which can produce efficient designs for trials with any number of stages and treatment arms.Since MAMS is relatively easy to understand and implement, we set out to explore these developments and to compare MAMS to other well established methods.We show how MAMS compares favourably with the more established combination method for some scenarios and explore how use of a novel selection rule may offer a further option within MAMS methodology. |
Seamless Study Designs & Real-time Data Capture Using Electronic Devices
| Rhian Jacob, Roche | Developing a new drug in a highly competitive environment necessitates a fast to market approach. This talk looks at the ongoing '944' trial, a multiple cohort seamless phase II/III study. Key study endpoints are captured using electronic devices, providing high volume of data in real-time. This talk describes the opportunities and challenges for a statistician leading a phase II readout within a phase III framework, with discussion on novel data capture methods; is the industry ready to handle device data? |
Training session: Explaining statistics to non-statisticians
| James Matcham, AstraZeneca / PSI Training Committee |
|
Introduction to Pharmacokinetics
| Laura Cope, Quanticate | Pharmacokinetics is the study of the effect of the body on the drug. The pharmacokinetic profile maps the concentration of the drug in the body over time tracking how the drug is absorbed, distributed, metabolised and excreted by individuals. Drug concentration is linked to both efficacy and safety and hence pharmacokinetic studies form the basis of much earlier phase clinical trials. Pharmacokinetic profiles are often described using summary measures such as the area under the curve (AUC) and the maximum concentration (Cmax) but how are these parameters derived? What models are used and what assumptions do they make? This presentation will describe the derivation of pharmacokinetic parameters for both intravenous and extravascular dosing, first looking at a single dose and then extending to multiple dosing schedules. |
AdePro – A new Perspective on Safety Profiles
| Nicole Mentenich, Christoph Tasto and Bastian Becker, Bayer AG | The database in a clinical trial contains vast information on adverse events, involving hundreds of different adverse event terms with varying severity grades and different start and end dates. Despite this plethora of information, insight into the adverse events in a clinical study is usually limited to simple summary tables of absolute and relative numbers of adverse event occurrences. AdEPro – an innovation of Bayer’s Biostatistics Innovation Center – is an unparalleled approach to audio-visualize the safety profile of both the individual patient and of the entire study cohort, which enables every study team member to experience the study and emphasize with the patients. The AdEPro app depicts the temporal progress of all adverse events in every study subject and enables the user to give profound answers to complex questions surrounding adverse events such as the frequency, duration and correlation of adverse events of interest. |
Marginal and conditional structural mean models for optimising Dynamic Treatment Regimes
| Nirav Ratia, GSK | Marginal structural models (MSMs) are casual models of dynamic treatment regimes (also known as treatment strategies or policies) designed to adjust for time-dependent confounding. These models are designed to adjust for exposures or treatment that vary over time, and standard approaches for adjustment of confounding can be biased when there exist time-dependent confounding. Dynamic treatment regimes (DTRs) provide the basis for statistical analysis in personalised medicine. A DTR is a decision rule that guides the treatment choices over the course of the therapy. The sequence of treatments a patient receives depends on the patient’s health status, response to prior treatment and other patient characteristics. |
An introductory course giving an overview of the pharmaceutical industry and the drug development process as a whole, aimed at those with 1-3 years' experience. It comprises of six 2-day sessions covering a range of topics including Research and Development, Toxicology, Data Management and the Role of a CRO, Clinical Trials, Reimbursement, and Marketing.
Our monthly webinar explores examples of innovative data visualisations relevant to our day to day work. Each month a new dataset is provided from a clinical trial or other relevant example, and participants are invited to submit a graphic that communicates interesting and relevant characteristics of the data.
Who is this event intended for? Statisticians with an interest understanding dose-finding in oncology. What is the benefit of attending? Learn about the state of oncology dose finding, particularly in light of current FDA guidance.
The book club’s usual focus is to read and discuss professional development books. In this short format event you can more easily develop you career without the commitment of reading the whole book - simply listen to the 1-hour long podcast before joining the interactive session on 21 May.
This webinar is organised by the RWD SIG and the Historical Data SIG. We will review recent methods, applications, and tools of integrating subject-level-data from clinical trial with external data using Bayesian methods and/or causal inference methods.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
This will be a 45 minute webinar which will explain the topic presented in the published paper, ‘Applying the Estimand Framework to Clinical Pharmacology Trials with a Case Study in Bioequivalance’. There will be 15 minutes for a panel Q&A with some of the authors following the presentation.
This will be a 45 minute webinar which will explain the topic presented in the published paper, ‘Applying the Estimand Framework to Clinical Pharmacology Trials with a Case Study in Bioequivalance’. There will be 15 minutes for a panel Q&A with some of the authors following the presentation.
This course is aimed at biostatisticians with no or some pediatric drug development experience who are interested to further their understanding. We will give you an introduction to the pediatric drug development landscape. This will include identifying the key regulations and processes governing pediatric development, a discussion on the needs and challenges when conducting pediatric research and a focus on the ways to overcome these challenges from a statistical perspective.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
The Institute of Cancer Research are seeking to appoint a Research Group Leader to join The CRUK Clinical Trials and Statistics Unit at the ICR.
This is an exciting, new opportunity for an experienced Statistician looking to take the next step in their career. Offered as a remote or hybrid position aligned with our site in Harrogate, North Yorkshire.
The BioMarin internship programme will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, whilst gaining an insight into the pharmaceutical/biotech industry.
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