Cover Image


Phenotypic Drug Discovery Trends 2015

出版商 HTStec Ltd 商品編碼 264599
出版日期 內容資訊 英文 50 Pages
商品交期: 最快1-2個工作天內
Back to Top
表型藥物研發趨勢:2015年 Phenotypic Drug Discovery Trends 2015
出版日期: 2015年09月21日 內容資訊: 英文 50 Pages


  • 報告摘要
  • 目次
  • 調查方法
  • 調查受訪者的組織&回答
  • 受訪者的企業或組織
  • 受訪者的出身地區
  • 受訪者的主要事業領域
  • 受訪者的工作職位
  • 目前PDD(表型藥物研發)的使用
  • PDD相關的理解、以及標的為基礎的發現差異
  • 受訪者所理解的PDD的最重要特徵
  • 受訪者的定義/表型篩選分析的理解
  • 表型篩選分析定義下的檢測類型
  • 做為標靶/使用表型篩選分析的疾病/治療領域
  • 採用PDD的主要動機
  • 調查結果摘要 (1)
  • 執行的主要課題
  • 表型篩選分析使用上的現在最大限制(障礙)
  • 限製表型篩選分析的採用的潛在障礙
  • 公司內部致力於PDD的職員(FTE)人數
  • 獲得支援的PDD企劃以及計劃數
  • 每年實驗的表型1次篩檢數
  • 表型每1次螢幕的Well數
  • 每進行的表型篩選分析的Well的平均成本
  • 最適合表型篩檢研究的細胞類型
  • 目前用於PDD調查的生物系統
  • 受訪者對表型篩檢的期待
  • 表型1次篩檢的平均成功率
  • 受訪者迄今取得的PDD計畫里程碑
  • 使用表型化驗的最佳地點
  • PPD使用以及偏好的目標分析方法
  • PDD相關協議聲明的層級
  • PDD開始的必要條件
  • 調查結果摘要 (2)
  • PDD的關鍵路徑為何?
  • PDD中應篩檢的化合物系列類型
  • PPD需要新的化合物資料庫嗎?
  • 表型檢測試劑&消耗品的年度預算
  • 表型檢測試劑&消耗品預算的詳細內容
  • 表型檢測試劑&消耗品市場預測
  • 表型檢測試劑&消耗品市場區隔
  • 表型檢測試劑&消耗品市場詳細內容
  • 優先使用或未來在PPD將被大幅使用的檢測技術&儀器類的平台、
  • PDD檢測試劑的主要廠商 (1)
  • PDD檢測試劑的主要廠商 (2)
  • PDD檢測試劑的主要廠商 (3)
  • PDD儀器類平台的主要廠商 (1)
  • PDD儀器類平台的主要廠商 (2)
  • PDD儀器類平台的主要廠商 (3)
  • PDD儀器類平台主要廠商的偏好
  • PDD上的未滿足需求以及促使表型篩選分析調查的必要新工具
  • 調查結果摘要 (3)



Executive Summary

This market report summarizes the results of HTStec's industry-wide global web-based benchmarking survey on phenotypic drug discovery (PDD) carried out in August 2015.

The survey was initiated by HTStec as part of its tracking of this emerging life science marketplace and to update HTStec's previous report on the subject (published March 2013).

The questionnaire was compiled by HTStec and attempts to meet the needs, requirements and interests of vendors hoping to address this space. The main objectives were to understand the latest thinking, current practices and preferences in PDD and future requirements for phenotypic primary screening.

The survey looked at the following aspects of PDD, as practiced today (2015) and in a few cases as predicted for the future (2017): current level of deployment (actual use); what features most highly in the understanding of PDD; definition of a phenotypic screening assay; assay types that are readily amenable to the target agnostic/biological mimetic approach; key diseases/therapeutic area(s) deploying phenotypic screening assays; main motivators for wanting to adopt PDD; key challenges of doing PDD; obstacles which would most limit the adoption of phenotypic screening assays today; number of FTE devoted in house to PPD; the number of primary phenotypic screens and wells per screen; the average cost per well of phenotypic screening assays; cell types most suited for phenotypic screening studies; biological systems currently used for PDD; expectations from phenotypic screening; success of PDD efforts to date; PPD project milestones achieved to date without knowledge of the target; where phenotypic assay approaches are best suited to be used; approaches used in pathway and target deconvolution; level of agreement with some statements about PDD; prerequisites for starting PDD; is there a critical path for PDD; type and size of compound libraries screened in PDD; does PDD require new types of compounds libraries; annual reagent and consumables budget for all work related to phenotypic assays and it breakdown into component parts; assay technologies and instrument platforms currently used in PDD; assay reagent and instrument platform vendors seen as key players in PPD; and any unmet needs in PDD or new tools are required to drive the investigation of phenotypic screening assays.

The main questionnaire consisted of 24 multi-choice questions and 6 open-ended questions. In addition, there were 6 questions related solely to survey demographics.

The survey collected 57 responses, of these 58% provided comprehensive input.

Responses were geographically split: 44% North America; 32% Europe; 14% Asia (excluding Japan & China); 5% Japan; and 2% China.

Survey respondents were drawn from persons or groups undertaking PDD and phenotypic primary screening. In addition feedback was sought from those interested in PPD and considering future investigation in this area.

Respondents represented 15 University; 13 Large Pharma; 7 Academic Screening Centers; 7 Research Institute; 6 Medium-Small Pharma; 3 Biotech Company; 3 Hospital/Clinic/Medical School; 1 Government Lab; 1 Not-For-Profit Research Center; and 1 Contract Research Organizations.

Most survey respondents had a senior job role or position which was in descending order: 11 principal investigators; 10 professors/assistant professors; 8 senior scientists/researchers; 7 directors; 6 section/ group leaders; 4 department heads; 3 research scientists; 2 others; 2 vice presidents; 2 post-docs; 1 lab manager; and 1 graduate/PhD student.

Respondents represented the followings main activities: 18 with a combination of drug discovery areas; 12 primary screening (HTS); 10 basic research; 5 assay development; 5 applied research; 3 other; 2 hits-to-leads (lead optimization); 1 leads-to-candidate (ADME Tox/preclinical research); and 1 therapeutic areas (target ID/validation).

Survey results were expressed as an average of all survey respondents. In addition, where appropriate the data was reanalysed after sub-division into the following 5 survey groups: 1) Pharma; 2) Biotech; 3) Academic Research; 4) Europe; and 5) North America.

90% of respondents were currently using PDD approaches (to varying extents) today. The remaining 10% were planning future investigation.

Captures bio content (targets presented in a physiological context) was ranked the most important features in understanding PDD.

The assay types used in a TTD application that are most amenable to the target agnostic/biological mimetic approach associated with PDD were assays involving primary cell cultures or co-cultures of primary cells.

The majority of respondents were targeting PDD within the oncology therapeutic area.

Allows for discovery of unexpected biology was ranked the main motivator for wanting to adopt PDD.

Mentalities are still target-orientated was rated as the key challenge (major issue) of doing PDD.

Understanding the biological endpoints needed was rated the main obstacle limiting adoption of phenotypic screening assays.

A median of 3 FTE's were allocated to enable/support in house PDD research (investigation and screening) in 2015.

A median of 3 different phenotypic projects/programs were undertaken in 2015.

A median of 3 phenotypic primary screens each with 10K-25K wells were done per year in 2015.

The median cost of a phenotypic screening assay undertaken in 2015 was $0.75-$1 per well.

Human primary cells were ranked the cell type most suited (relevant) for phenotypic screening studies.

Cell line monocultures were the biological system currently most used to investigate PDD.

Novel MOA which is differentiated from the standard of care and to understand the functional responses were both equally rated as most likely (desired) outcomes for phenotypic screening.

The median success rate for phenotypic primary screening in 2015 was 50%.

SAR observed in phenotypic assay system was the PDD project milestone most achieved to date without knowledge of the target.

Suitability for the identification of novel therapeutically active molecules for drug discovery was ranked the most important use of phenotypic assays.

Signal pathway activity mapping methods were ranked the target deconvolution approach most used for the identification of phenotypic activities today.

Respondent's level of agreement with certain statements about PDD was recorded.

Most respondents think there is a critical path for PDD and suggested some of the steps involved.

Annotated compounds (compounds with known targets/mechanisms) was rated the type of compound collection that should be most screened in PDD.

The median size of compound libraries most evaluated for PDD today (2015) was 10K-50K compounds.

Most respondents don't know enough to comment if PDD requires new types or more diverse compound libraries.

A median budget of $50K-$100K/lab was allocated for phenotypic assay reagents and consumables in 2015, with the greatest share allocated to assay specific reagents.

A bottom-up model developed around respondent's % use of phenotypic screens and their annual budget for phenotypic assay reagents and consumables estimated the global market to be around $165M in 2015.

The most preferred key vendors of assay reagents used in PDD were Thermo Scientific, Cell Signaling Technology and Promega.

The most preferred key vendors of instrument platforms used in PDD were PerkinElmer, Molecular Devices and Thermo Scientific.

Respondent's feedback on the following open-ended questions were documented: 1) What is understood by PDD, how does it differ from target-based discovery? 2) What defines a phenotypic screening assay? 3) What are the biggest limitations (obstacles) in using phenotypic screening assays today? 4) What are the prerequisites for starting PDD? 5) What assay technologies and instrument platforms are preferentially used for PDD? and, 6) What are the biggest unmet needs in PDD and what new tools are required to drive the investigation of phenotypic screening assays?

The full report provides the data, details of the breakdown of the responses to each question, its segmentation, estimates for the future (2017) and CAGR estimates. It also highlights some interesting differences between the survey groups.

Table of Contents

  • Executive Summary
  • Table of Contents
  • Survey Methodology
  • Organisation & Response Of Survey Participants
  • Respondent's Company Or Organisational Origin
  • Respondent's Geographic Origin
  • Respondent's Main Group Activity
  • Respondent's Job Role
  • Current Use of PDD
  • Understanding Of PDD And How It Differs From Target-Based Discovery
  • Most Important Features In Respondent's Understanding Of PDD
  • Respondents Definition/Understanding Of A Phenotypic Screening Assay
  • Assay Types In Respondent's Opinion That Are Most Amenable To PDD
  • Disease/Therapeutic Areas Targeting/Using Phenotypic Screening Assays
  • Main Motivators For Wanting To Adopt PDD
  • Summary Of Survey Findings (1)
  • Key Challenges Of Doing PDD
  • Biggest Limitations (Obstacles) In Using Phenotypic Screening Assays Today
  • Potential Obstacles Limiting Adoption Of Phenotypic Screening Assays
  • No. Of FTE's Devoted In House To PDD
  • No. Of PDD Projects Or Programs Supported
  • No. Phenotypic Primary Screens Run Per Year
  • No. Of Wells Per Phenotypic Primary Screen
  • Average Cost Per Well Of Phenotypic Screening Assays Undertaken
  • Cell Types Most Suited For Phenotypic Screening Studies
  • Biological Systems Currently Used To Investigate PDD
  • Respondent's Expectations For Phenotypic Screening
  • Average % Success Rate For Phenotypic Primary Screens
  • PDD Project Milestones Respondents Have Achieved To Date
  • Where Phenotypic Assays Are Most Suited To Be Used
  • Target Deconvolution Approaches Used Or Preferred For PDD
  • Level Of Agreement On Statements About PDD
  • What Are The Prerequisites For Starting PDD?
  • Summary Of Survey Findings (2)
  • Is There a Critical Path For PDD?
  • Types Of Compound Collection That Should Be Screened In PDD
  • Size Of Compound Libraries Most Evaluated For PDD
  • Does PDD Require New Compound Libraries?
  • Annual Reagent & Consumables Budget For Phenotypic Assays
  • Breakdown Of Phenotypic Assay Reagent & Consumables Budget
  • Phenotypic Assay Reagents & Consumables Market Estimate
  • Phenotypic Assay Reagents & Consumables Market Segmentation
  • Breakdown Of Phenotypic Assay Reagents & Consumables Market
  • Assay Technologies & Instrument Platforms Preferentially Used Or Expect To Make Greatest Use In The Future For PDD
  • Key Vendors Of PDD Assay Reagents (1)
  • Key Vendors Of PDD Assay Reagents (2)
  • Key Vendors Of PDD Assay Reagents (3)
  • Key Vendors Of PDD Instrument Platforms (1)
  • Key Vendors Of PDD Instrument Platforms (2)
  • Key Vendors Of PDD Instrument Platforms (3)
  • Biggest Unmet Needs In PDD & What New Tools Are Required To Drive The Investigation Of Phenotypic Screening Assays
  • Summary Of Survey Findings (3)
Back to Top