TIME LAPSE BY VITROLIFE: PRIMO VISION. Brett Glazar, M.S. Lab Manager/Senior Embryologist

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TIME LAPSE BY VITROLIFE: PRIMO VISION Brett Glazar, M.S. Lab Manager/Senior Embryologist

DISCLOSURES Employee at Vitrolife MEA Lab Manager R&D team; responsible for U.S. Regulatory Submissions and clinical data management Primo Vision and the microwell dish are not yet FDA approved for clinical use in the U.S. Microwell dish is pending FDA approval Primo Vision is approved (CE) for use in Europe, Canada and Mexico

AGENDA The Primo Vision concept Primo Vision microwell dish Computerized embryo monitoring Scientific evidence Summary

THE PRIMO VISION CONCEPT

TIME-LAPSE EMBRYO MONITORING A continuous monitoring brings more to the morphological assessment

PRIMO VISION A time-lapse system providing safe culture in your incubator

EMBRYO EVALUATION WITHOUT OPENING THE DOORS OF YOUR INCUBATOR

OPTICS COMPLETELY SEPARATED FROM CONTROLLING AND ANALYSIS Culturing environment Controlling unit Capture and Analysis

STATE-OF-THE-ART IMAGE QUALITY Stereo Microscope 3D Familiar Comparable? Primo Vision Microscope Hoffmann contrast optics Wide field of view 1 micron /pixel 5 megapixel CCD chip

MODULAR SYSTEM SIZE IT AFTER YOUR NEEDS Let your time-lapse system grow with you For research For some patients For all

GROUP CULTURE ENVIRONMENT

PRIMO VISION EMBRYO CULTURE DISH Individually monitored embryos in improved group culture system Custom designed and manufactured Sterile, disposable Group culture in microwells 9 or 16-well edition CE 93/42 marked and officially one-cell mouse embryo tested (MEA) Specially adjusted for in vitro culture in Primo Vision System Provides significantly better culture environment than traditional culturing 1,2 1 Ergin E. et al., Turkey, ESHRE 2014 2 Fancsovits P. et al., Hungary, ALPHA 2014)

OPTIMIZED CULTURE Individually monitored embryos in improved group culture system Improved culture Individual Monitoring Embryos developing: In their own microenvironment Under a common microdroplet 9-16 embryos Rim for stable carrying Orientation sign Alphanumeric well identification

COMPUTERIZED EMBRYO MONITORING

COMPUTERIZED EMBRYO MONITORING Offers new possibilities Automated image capturing: 5-10 minutes capture intervals Annotate embryos development manually Compare and rank the embryos by their potential according to latest science Create personalized reports Follow your embryos remotely from your office or computer Share results via video and ipad Create an archive of all your result a perfect base for research

ANNOTATE IMPORTANT TIMINGS In an easy Play and click -way

COMPARING IS EASY Follow your best embryos separately Cleavage times Interphases between cleavages Review events Measurements

REPORTS ARE CREATED AUTOMATICALLY A simple way of archiving

FEEL FLEXIBLE MONITOR AND ANALYZE WHERE YOU ARE

SCIENTIFIC EVIDENCE

TIME-LAPSE MONITORING SIGNIFICANTLY INCREASED PREGNANCY RATES STUDY DESIGN Prospective cohort trial 239 women ( 42 y) undergoing ICSI cycles Patients randomized into TLM group (30%) or Conventional group (70%) 2- or 3-day culture TLM group: Primo Vision dishes Conventional group: Nunc dishes Evaluation and selection for transfer 1-3 embryos transferred per patient TLM group: Without removing the embryos from the incubator t2, t3, t4, t5, t8; cc2, cc3; s2, s3 Conventional group: Morphological evaluation at 44h and 68 h Morphokinetic parameters of early embryo development via timelapse monitoring and their effect on embryo selection and ICSI outcomes: a prospective cohort study (Siristatidis C. et al., Greece; J assist reprod genet)

TIME-LAPSE MONITORING SIGNIFICANTLY INCREASED PREGNANCY RATES OUTCOME OUTCOME IN PATIENTS > 40 Y 80 80 TLM group 70 TLM group 60 40 Conventional group 60 50 40 Conventional group 30 20 20 10 0 Gestational sac (%) Fetal heart beat (%) 0 Gestational sac (%) Fetal heart beat (%) Morphokinetic parameters of early embryo development via timelapse monitoring and their effect on embryo selection and ICSI outcomes: a prospective cohort study (Siristatidis C. et al., Greece; J assist reprod genet)

CLEAVAGE PATTERN PREDICTS DEVELOPMENTAL POTENTIAL OF DAY 3 HUMAN EMBRYOS PRODUCED BY IVF 1 Retrospective analysis for model building 345 embryos were studied for abnormalities in division behaviour Two categories formed, based on the impact of abnormal division behaviours on daughter cells (whether they take part in blastocyst formation or not) CATEGORY 1 abnormal division behaviours with low impact on blastocyst formation: Distorted cytoplasmic movement Uneven blastomeres Big fragment CATEGORY 2 abnormal division behaviours with high impact on blastocyst formation: Developmental arrest Direct cleavage Disordered division Fragmentation Yang S.T. et al., China; Reprod Biomed Online, 2015

CLEAVAGE PATTERNS OF THE FIRST THREE CLEAVAGE CYCLES CAN PREDICT THE DEVELOPMENTAL POTENTIAL OF EMBRYOS ON D3 2 Prospective observational study Implantation rate Based on the retrospective study results a hierarchical classification model was developed Embryos were classified into Grade A F, based on the type of abnormal division: Belongs to Category 1 or 2? Occurs in 1st, 2nd or 3rd cleavage cycle? Correlation of embryo grade and implantation was studied in 144 KID embryos of 70 women Significant decrease in the implantation rate of embryos of lower grades 70% 60% 50% 40% 30% 20% 10% 0% Grade A Grade B Grade C Grade D (Grade E and F embryos were not transferred) Yang S.T. et al., China; Reprod Biomed Online, 2015

STUDIES SUPPORTING GROUP CULTURE

COMPARISON OF CULTURE IN GROUP IN A MICROWELL GROUP CULTURE DISH OR INDIVIDUALLY IN DROPLETS Results from an intermediate analysis Prospective randomized study Comparison of group culture vs individual culture 3-day culture Group culture in Primo dish 211 transferred embryos Individual culture 209 transferred embryos Fancsovits P. et al., Hungary, Alpha 2014

GROUP CULTURE IN PRIMO DISH ALLOWS SIGNIFICANTLY BETTER CULTURE CONDITIONS FOR THE EMBRYOS Higher proportion of embryos available for cryopreservation (p=0.002) Higher clinical pregnancy rate 54.5% vs. 45.9% (p=0.06) 6 5 Microwell group culture 60.00% 50.00% Microwell group culture (N=211) 4 3 Individual culture 40.00% 30.00% Individual culture (N=209) 2 20.00% 1 10.00% 0 Number of embryos cryopreserved 0.00% Clinical pregnancy % Fancsovits P. et al., Hungary, Alpha 2014

COMPARISON OF SINGLE EMBRYO CULTURE OF GROUP CULTURE USING A MICRO-WELL GROUP CULTURE DISH Prospective randomized study 5-day culture group culture (85 embryos) vs individual culture (85 embryos) in the same dish Group culture in the Primo dish higher expanded blastocyst rate (p=0.0025) higher proportion of A grade ICM and TE (p<0.0001, p=0.0007) higher rate of embryo utilisation (p=0.017) Ergin E. et al., P 117 Randomized controlled comparison of single embryo culture versus group culture using a micro-well group culture dish in humans, ESHRE 2014

GROUP CULTURE IN PRIMO DISH ALLOWS SIGNIFICANTLY BETTER CULTURE CONDITIONS FOR THE EMBRYOS 60% 50% 40% 30% p=0.0025 p=0.017 Group culture in microwell dish Individual culture 20% 10% 0% Blastocyst development % Embryo utilisation % Ergin E. et al., P 117 Randomized controlled comparison of single embryo culture versus group culture using a micro-well group culture dish in humans, ESHRE 2014

SUMMARY

SUMMARY Good for the embryo Stable conditions Reduced handling Controlled environment Good for the embryologist Catch abnormal cleavages Improved selection and deselection Easy to use system Good for the clinic Modular, flexible system Improved workflow QC tool Archiving tool Service tool Attila, born in May, 2010 World s first time-lapse baby assessed with Primo Vision V2