Presentation is loading. Please wait.

Presentation is loading. Please wait.

In Vitro Safety Profiling During Lead Optimisation

Similar presentations

Presentation on theme: "In Vitro Safety Profiling During Lead Optimisation"— Presentation transcript:

1 In Vitro Safety Profiling During Lead Optimisation
Murray Brown Manager, Data Interpretation and Business Process Screening and Compound Profiling

2 Drug Discovery Process
Target Selection Candidate Selection IND filing NDA filing Basic Research Lead Discovery Preclinical Development Clinical Development FDA Filing 3 1 6 1.5 Years Once a candidate is selected the pharmacological properties of the molecule are fixed High Throughput Screening approaches apply within Lead Discovery to: Reduce the cycle time from target selection to candidate selection Increase the number of candidates per program Increase the quality of candidates selected

3 Strategies to Improve the Quality of Lead and Candidate Generation
Robust screening infrastructure Automation quality control Statistical methods for hit selection Quality “drug-like” compound libraries Low molecular weight and cLogP New Screening Paradigms Fragment Screening Encoded Library technology Relevant assay biology Native cellular systems Biophysical Screening Pharmacology of lead series Ability to assess on-target and off-target activity

4 Causes of Attrition – Safety & Efficacy
Reasons For NME Termination By Stage Industry Portrait KMR Terminology Early Dev: Preclin up to Ph III Start Late Dev: Start Ph III to Launch KMR Group R&D General Metrics Study Final Report July 1, 2010

5 Addressing the Challenge of Drug Safety in Early Discovery
Vision To increase candidate quality and probability of clinical success through the identification and mitigation of safety hazards in chemical series prior to candidate selection Strategy Using high throughput techniques, implement panels of assays for use in early discovery that identify likely safety liability in hits, leads and candidates

6 Attrition Reduction Activities in GSK
Strategic Intent Implement assays during H2C to identify and manage compound series likely to cause toxicity in preclinical or clinical studies Assays configured during with capacity to screen 1200 hits, leads and candidates/year eXP Cardiotoxicity Hepatotoxicity Genotoxicity A bi-weekly panel of 50 molecular target assays with known clinical liability A panel of Ion Channel assays enabled by high throughput electrophysiology GreenScreen assay licensed to identify Genotoxicants Cell Health assay detects 70% of known hepatotoxicants

7 eXP (enhanced cross screen panel)
Neuronal: a1b3g2 GABA SERT DAT NET M1 MAO-B μopioid κopioid Dopamine 1 Dopamine 2 Histamine 1 NK1 Cardiac/vascular: KCNQ1/minK L-type Ca VR4 M2 Adenosine 2a β2 adrenergic α1b adrenergic α2a adrenergic Nav1.5 Kv1.5 5-HT1B 5-HT2A 5-HT2C COX2 V1a Hepatic: OATP1B1 PXR Gastro-intestinal: 5-HT3 PDE4B GSK3b PI3k Neuromuscular: a1bgd nAChR Immunological: LCK Cannabinoid 2 11 point dose response curve Functional/activity assays

8 Interpharma Safety Profiling
Knowledge-Sharing - Secondary Pharmacology Screening AstraZeneca Joanne Bowes GlaxoSmithKline Andrew Brown Arun Sridhar Outcomes: Poster at SPS meeting: Rational design of an in vitro safety profiling panel to reduce undesired secondary pharmacology of drug candidates. Steven Whitebread, Joanne Bowes, Andrew Brown, Jacques Hamon, Wolfgang G. Jarolimek, Gareth Waldron and Arun Sridhar Journal of Pharmacological and Toxicological Methods; 64(1), July-August 2011, Page e18. Manuscript - in preparation 2009-present What Targets? What Technologies? What Process? Shared Case Studies Pfizer Gareth Waldron Novartis Steven Whitebread Jacques Hamon Pharmaxis Wolfgang Jarolimek

9 (IonWorks® and PatchXpress®)
High Throughput Electrophysiology Assays to predict Functional Cardiotoxicity Cardiac Ion Channels CNS (GABAA) (Barracuda) hERG NaV1.5 CaV1.2 KV1.5 KCNQ1 (IonWorks® and PatchXpress®) See posters by Metul Patel et al on hERG IonWorks® population patch clamp and Joanna Taylor et al on stem cell derived Cardiomyocytes

10 Genetic Toxicology: The GreenScreen Assay
Genotoxic agents either react directly with DNA or disrupt the cellular apparatus which regulate the fidelity of the genome Regulations require a minimum of 3 GLP tests: a test for gene mutation in bacteria (for example, the Ames test), a test for chromosomal aberrations in vitro or the MLA an in vivo test for chromosomal damage in rodent haematopoietic cells. The GADD45a gene is upregulated in response to DNA damage in the GreenScreen assay (Gentronix) Reporter transfected into Human p53 competent lymphoblastoid cells

11 Genetic Toxicology: GreenScreen Assay
15% of pre-candidates are terminated due to Genotoxicity GSK has licensed the GreenScreen HC genotoxicity assay for profiling of hits, leads and candidates 31 of 34 known genotoxic agents induced GADD45a reporter 41 of 41 non-genotoxic agents did not induce the GADD45a reporter Early stage (HitID and SoC) identification of GreenScreen HC actives enable LO chemistry to focus on molecules without this liability BlueScreen HC has now been implemented to allow higher throughput See poster by Kate Simpson et al on BlueScreen assay validation

12 Cell Health Assay to Detect Hepatotoxicants
Drug-Induced Liver Injury (DILI) is a recurrent problem in pharmaceutical development Idiosyncratic hepatotoxicity is one of the leading causes of drug withdrawals, non-approvals and warnings (Kaplovitz 2005) Can we identify hepatotoxicants prior to candidate selection and reduce attrition due to pre-clinical or clinical hepatotoxicity? 96well assay using HepG2 (Human liver carcinoma) cells

13 GSK Cell Health Assay Description
Measures cytotoxic effect of compounds in human liver-derived HepG2 cells in 384-well format 3 parameter automated imaging assay Using fluorescent staining, the key parameters measured in this assay are : - Nuclear Condensation Hoechst 33342 Cell permeable DNA binding dye Mitochondrial membrane potential TMRM Accumulates in healthy Mitochondria but leaks out when mitochondrial membrane potential is discharged Membrane permeability TOTO-3 Cell membrane impermeable nuclear stain Impaired mitochondrial function is an early indicator of cell injury whereas loss of membrane integrity and changes in nuclear morphology are indicators of acute or late stage cytotoxicity. Quantification is carried out using the InCell

14 Mitochondrial Potential Membrane Permeability
Example images Mitochondrial Potential Membrane Permeability Nuclei Negative Control Postive Control

15 Typical dose response curves

16 Correlation between Cell Health readouts
Compounds usually show very similar IC50s in all 3 readouts, but there are exceptions where toxicity is specific to a single readout

17 Cell Health Assay to Detect Hepatotoxicants
The Cell Health assay for profiling of hits, leads and candidates Negative compounds /28 Human and rat hepatotoxicants 29/30 Cytotoxicants 4/4 Idiosyncratic human hepatotoxicants 3/18 Early stage elimination of Cell Health actives enable LO chemistry to focus on molecules without this liability Concentration Compound A failed due to liver toxicity. No reported hepatotoxicity for Compounds B and C. A B C 150 125 100 75 50 25 -25 -50 5E-7 1E-6 5E-6 1E-5 5E-5 0... 0.0... 5E-7 1E-6 5E-6 1E-5 5E-5 0... 0.0... 5E-7 1E-6 5E-6 1E-5 5E-5 0... 0....

18 Frequency of toxicity in Cell Health for marketed drugs and failed clinical candidates
Inactive in Cell Health Failed Candidates twice as likely to be active in Cell Health than marketed drugs Significant proportion of marketed drugs show toxicity in Cell Health Active in Cell Health Drugs Failed Development Candidates

19 Toxic compounds? Toxic dose
Phillippus Aureolus Theophrastus Bombastus von Hohenheim ( ) Paracelsus Alle Ding' sind Gift, und nichts ohn' Gift; allein die Dosis macht, daß ein Ding kein Gift ist. "All things are poison and nothing is without poison, only the dose permits something not to be poisonous."

20 Cell Health cytotoxicity vs normal and toxic exposure levels
Therapeutic or ‘normal’ blood concn Toxic blood concn 100 uM Exposure level 1 uM 10 nM 100 uM Cell Health pIC50 10 uM Therapeutic and toxic blood concentrations of more than 800 drugs and other xenobiotics M. Schulz, A. Schmoldt Pharmazie 58(7)

21 What drives cytotoxicity? i) Physchem properties - clogP

22 What drives cytotoxicity? ii) Physchem properties – rotatable bonds

23 What drives cytotoxicity? iii) chemical series
Cell Health cytotoxicity by chemical cluster clogP distribution for each cluster clogP vs Cell Health pIC50 Cell Health pIC50

24 Cell Health Cytotoxicity is SAR-able in lead optimisation
Physicochemical properties can be manipulated to reduce likelihood of Cell Health cytotoxicity ↓clogP, ↓# aromatic rings, ↓heavy atom count (or ↑ >50!), ↑ heteroatoms, ↓ rotatable bonds Cell Health cytotoxicity is a feature of chemical series beyond their physicochemical properties (toxicophores) Early screening in Cell Health assay at HitID allows selection of series with lower likelihood of cytotoxicity

25 Cell Health Assay Related to Promiscuity in eXP
Green = Inactive in Cell Health Red = Active in Cell Health

26 In vitro cross screening profile of selected drugs
Low promiscuity, mechanism based toxicity detected by eXP, non-toxic in Cell Health Non-promiscuous, highly tolerable, non-toxic in Cell health a2C a1B b2 Moderately promiscuous and highly tolerable, non-toxic in Cell health Highly promiscuous, low tolerability, toxic in Cell Health CB2 Ag Assay

27 Attrition Reduction Toolkit: An annotated one-stop-shop for all attrition reduction assays at GSK

28 Attrition Reduction Toolkit: An annotated one-stop-shop for all attrition reduction assays at GSK
Compound Structure


30 Profile similarity in eXP

31 Conclusions We have implemented a panel of assays in early discovery to assess toxicity hazards in hit and lead series Assays are annotated according to likely clinical effect Each assay is not decision making in isolation Data enables comparative decisions between chemical series Activity in multiple assays needs to be considered Assays can be used to drive SAR Cell Health assay in HepG2 cells concords well with physicochemical properties shown to be important in clinical attrition and clinical in vivo tolerability Exposure levels are key for toxicology (as well as efficacy) expected dose is important factor to be included in interpretation of early Safety Profiling data

32 Acknowledgements Steve Rees (formerly Screening and Compound Profiling) Andrew Brown (Screening & Compound Profiling) Dave Morris (Screening & Compound Profiling) Wolfgang Jarolimek (formerly Screening and Compound Profiling) Joanna Taylor (Screening & Compound Profiling) Kate Simpson (Screening & Compound Profiling) Metul Patel (Screening & Compound Profiling) Rob Jepras (Screening & Compound Profiling) Rob Eagle (Screening & Compound Profiling) Darren Green (Computational & Structural Chemistry) Cerys Lovatt (Safety Assessment) Julie Holder (Safety Assessment/Stem Cells) Nick McMahon (Safety Assessment) Paul Hastwell (Safety Assessment) Patrick Wier (Safety Assessment) Steve Clarke (DMPK) Bob Hertzberg (Screening & Compound Profiling) Many other GSK scientists responsible for generating the assays and data

Download ppt "In Vitro Safety Profiling During Lead Optimisation"

Similar presentations

Ads by Google