Skip to content
Precision for Medicine
Press Release

FDA Veteran Paz Vellanki, MD, joins Precision to become one of 3 ex-FDA oncology leaders supporting clients

false
Blog

Clinical Biostatistics

100% sourced from leading minds on the front lines of research

Latest Posts

  • Read: Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies

    Clinical Trials

    Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1774960559659, hs_published_at=1787681149919, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1775839468505, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, position=Director, Biostatistics, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Kurt Preugschat avatar

      Kurt Preugschat

    Discover
  • Read: Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM) Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

    Clinical Trials

    Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1774960559659, hs_published_at=1787681149919, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1775839468505, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, position=Director, Biostatistics, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Kurt Preugschat avatar

      Kurt Preugschat

    Discover
  • Read: Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM) Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

    Clinical Trials

    Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1774960559659, hs_published_at=1787681149919, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1775839468505, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, position=Director, Biostatistics, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Kurt Preugschat avatar

      Kurt Preugschat

    Discover
  • Read: Administering Event-Driven Clinical Trials: A Biostatistical Analysis Administering Event-Driven Clinical Trials: A Biostatistical Analysis

    Clinical Trials

    Administering Event-Driven Clinical Trials: A Biostatistical Analysis

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1774960559659, hs_published_at=1787681149919, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1775839468505, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, position=Director, Biostatistics, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Kurt Preugschat avatar

      Kurt Preugschat

    Discover
  • Read: Inside a CRO: The Impact of a Biostatistician in Clinical Research Analyzing the Impact of a Biostatistician

    Clinical Trials

    Inside a CRO: The Impact of a Biostatistician in Clinical Research

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778868, hs_child_table_id=0, hs_updated_at=1715694281220, hs_published_at=1787681149919, description=Paul Pappas is a Senior Director of Biostatistics, bringing more than 20 years of experience to the team. His experience includes phase I-IV clinical trials as well as observational prospective cohort and registry studies. His therapeutic experience encompasses Autoimmune diseases, Cardiology, CNS, Infectious diseases, medical devices, Oncology, Rare diseases, and Vaccines. Paul has also co-authored over 30 manuscripts published in peer-reviewed medical journals., avatar=Image{width=626,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Paul-Pappas.png',altText='Paul-Pappas',fileId=167378452645}, linkedin=https://www.linkedin.com/in/paul-pappas-86176ab, hs_name=, hs_path=, lastname=Pappas, hs_initial_published_at=1775839468505, hs_created_at=1709645745099, hs_is_edited=false, hs_deleted_at=0, name=Paul, job=, slug=paul-pappas, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Paul Pappas avatar

      Paul Pappas

    Discover
  • Read: Best Practices for Biostatisticians: Preparing for Interim Analysis in Clinical Trials biostatisticians

    Clinical Trials

    Best Practices for Biostatisticians: Preparing for Interim Analysis in Clinical Trials

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778868, hs_child_table_id=0, hs_updated_at=1715694281220, hs_published_at=1787681149919, description=Paul Pappas is a Senior Director of Biostatistics, bringing more than 20 years of experience to the team. His experience includes phase I-IV clinical trials as well as observational prospective cohort and registry studies. His therapeutic experience encompasses Autoimmune diseases, Cardiology, CNS, Infectious diseases, medical devices, Oncology, Rare diseases, and Vaccines. Paul has also co-authored over 30 manuscripts published in peer-reviewed medical journals., avatar=Image{width=626,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Paul-Pappas.png',altText='Paul-Pappas',fileId=167378452645}, linkedin=https://www.linkedin.com/in/paul-pappas-86176ab, hs_name=, hs_path=, lastname=Pappas, hs_initial_published_at=1775839468505, hs_created_at=1709645745099, hs_is_edited=false, hs_deleted_at=0, name=Paul, job=, slug=paul-pappas, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Paul Pappas avatar

      Paul Pappas

    Discover
  • Read: Phase III Case Study: Adapting in the Face of Adversity Phase III Case Study

    Clinical Trials

    Phase III Case Study: Adapting in the Face of Adversity

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778845, hs_child_table_id=0, hs_updated_at=1754641622943, hs_published_at=1787681149919, description=Brian Beus is a Principal Biostatistician with more than 25 years experience supporting the statistical analysis of data through all phases of clinical trials across many therapeutic areas. He has extensive experience in leading teams and working with sponsors through study design, protocol development, adaptive design, statistical analysis plans, statistical analysis, clinical study reports, regulatory submissions, and regulatory responses., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/brian-beus.png',altText='brian-beus',fileId=194097831688}, linkedin=https://www.linkedin.com/in/brian-beus-66033333, hs_name=, hs_path=, lastname=Beus, hs_initial_published_at=1775839468505, hs_created_at=1709645745076, hs_is_edited=false, hs_deleted_at=0, name=Brian, job=, slug=brian-beus, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Brian Beus avatar

      Brian Beus

    Discover
  • Read: Pros and Cons: Innovative Study Designs vs. Traditional FIH Study Designs vs. Traditional FIH

    Clinical Trials

    Pros and Cons: Innovative Study Designs vs. Traditional FIH

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778854, hs_child_table_id=0, hs_updated_at=1715695005945, hs_published_at=1787681149919, description=Rosa Canals López has 15 years of experience in managing Phase I-IV clinical trials, including >7 years of Clinical Management experience. Her focus is on Phase I studies and CAR-T, with additional experience in oncology, hematology, pediatrics, infectious diseases, cardiology, and nephrology., avatar=Image{width=533,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Rosa-Canals.png',altText='Rosa-Canals',fileId=167374630834}, linkedin=https://www.linkedin.com/in/rosa-maria-canals-l%C3%B3pez-74902194, hs_name=, hs_path=, lastname=Canals López, hs_initial_published_at=1775839468505, hs_created_at=1709645745085, hs_is_edited=false, hs_deleted_at=0, name=Rosa, job=, slug=rosa-canals-lópez, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Rosa Canals López avatar

      Rosa Canals López

    Discover
  • Read: Overview: Innovative Study Designs vs. Traditional FIH Innovative Study Designs vs. Traditional FIH

    Clinical Trials

    Overview: Innovative Study Designs vs. Traditional FIH

    |
      has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778854, hs_child_table_id=0, hs_updated_at=1715695005945, hs_published_at=1787681149919, description=Rosa Canals López has 15 years of experience in managing Phase I-IV clinical trials, including >7 years of Clinical Management experience. Her focus is on Phase I studies and CAR-T, with additional experience in oncology, hematology, pediatrics, infectious diseases, cardiology, and nephrology., avatar=Image{width=533,height=710,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Rosa-Canals.png',altText='Rosa-Canals',fileId=167374630834}, linkedin=https://www.linkedin.com/in/rosa-maria-canals-l%C3%B3pez-74902194, hs_name=, hs_path=, lastname=Canals López, hs_initial_published_at=1775839468505, hs_created_at=1709645745085, hs_is_edited=false, hs_deleted_at=0, name=Rosa, job=, slug=rosa-canals-lópez, email=, hs_updated_by_user_id=65712240}, second={}, third={}})
    • Rosa Canals López avatar

      Rosa Canals López

    Discover
Loading...
You've reach the end