Science Pool

Challenges in Biomanufacturing and How Just-Evotec Biologics Plans to Overcome Them

Posted by Evotec on Jan 9, 2024 11:06:01 AM

Watch the 20 minute interview with Jon Gunther, VP Business Development Just-Evotec Biologics, at Biomanufacturing World Summit 2023. For a complete table of content regarding Jon's discussion, please see below.

Table of Contents

0:00 min – 01:50 min
Intro + Discussion on biomanufacturing costs and making biotherapeutics more affordable and accessible to patients worldwide

01:51 min –5:06 min
Emergence of continuous manufacturing of biologics to reduce cost of goods manufacturing (COGM)

5:07 – 7:00 min
Switching from fed-batch to continuous manufacturing, quality requirements and stance of the FDA

7:01 – 08:32 min
Timelines for switching to continuous manufacturing

08:33 –10:42 min
Pharma 4.0 / Using state-of-the-art technology incl. lights-out manufacturing approach

10:43 – 13.42 min 
Highly flexible manufacturing approach with Just-Evotec Biologics’ J.POD cGMP manufacturing facilities in North America and Europe

13.43 – 16:30 min
What should commercial partners observe in terms of cost, quality, scale-up and how this process can be de-risked

16:31 – 17:30 min
J.POD’s flexible and de-risked manufacturing approach when going from late-stage clinical to commercial supply

17:31 – 19:44
Our flexible partnership model incl. options like with our tech partnership with Sandoz for biosimilars development and commercial manufacturing

19:45 – end
Closing comments, get in touch with us!

Watch Now

Tags: Videos & Webinars, Biologics

A Spotlight on Aging Webinar series

Posted by Evotec on Sep 19, 2023 1:43:54 PM

Watch on demand now!

Our 3 part "Spotlight on Aging" webinar series is now available to stream on demand.

In the last fifty years, life expectancy has increased dramatically thanks to advances in science, medicine, and public awareness. The population is living longer, but with it comes the challenge of improving Healthy Life Expectancy.

Join our speakers in our innovative 3-part webinar series where they will openly discuss 3 key topics:

  • Therapeutic approaches for aging and age-related disease
  • Aging and precision medicine
  • Why older adults should not be underrepresented in clinical trials. 

WATCH ON DEMAND


Tags: Videos & Webinars, In vitro Biology, Proteomics, Metabolomics & Biomarkers, Age-Related Diseases, Clinical Development

Deep Proteomics Webinar

Posted by Evotec on Apr 4, 2023 10:10:27 AM

A novel approach for deep proteomic insight across different biofluids:
Human body fluids provide a rich source of information that can be used to predict a patient’s disease state and guide drug development or personalized therapies.

In this joint webinar with Seer we show how the combination of the Proteograph Product Suite and high-end mass spectrometry provides unbiased access to thousands of proteins that have not been detectable by conventional proteomics techniques.

Learn More

Tags: Videos & Webinars, Proteomics, Metabolomics & Biomarkers

Webinar on demand Immuno-Oncology: Harnessing the immune system to fight cancer

Posted by Evotec on Oct 19, 2022 10:39:15 AM

With game changer therapies and unprecedented clinical successs for patients, Immunotherapy has becomes an essential pillar for cancer treatment. During this webinar, Michael Esquerre, our VP, In Vitro Biology, discusses how the team at Evotec are pusing Immuno-Oncology drug discovery, playing with multi-therapeutic modalities. Stream it on demand now!

Watch Now

Tags: Oncology, Videos & Webinars, In vitro Biology

Using RIS to Improve Risk Assessment of CYP Induction

Posted by Evotec on Jul 12, 2022 12:25:10 PM

Watch the webinar to learn more about recent updates in CYP induction!

 


About the Webinar

Cytochrome (CYP) P450 induction is a well-established mechanism for increased prevalence of DDIs. Whilst its study in vitro has been described in regulatory guidance for over 20 years, data interpretation methods and details for study design have evolved and the best approaches for study of small molecules and other therapeutics are still being discussed within CROs, pharma and biotechs.

In this webinar our expert, Katie Plant, describes the most recent updates in CYP induction. By reviewing and consolidating literature and recent perspectives from Innovation and Quality Induction Working Group (IQ IWG) alongside the regulatory guidance, this provides a comprehensive overview and outlines the recommended approach to assess CYP induction in vitro. When supported by well-designed in vitro assays and batch qualification using a known set of CYP3A4 inducers, relative induction score (RIS) correlation analysis serves as a useful tool enabling the magnitude of clinical CYP3A4 induction to be predicted and used to support decision-making for investigating potential DDI risk.


About the Speaker

 

Plant,KatieRSZ

Katie Plant

Principal Scientist | Cyprotex Discovery Ltd

Katie Plant is a Principal Scientist in the Drug Metabolism group at Cyprotex, UK, responsible for operational delivery of high-throughput screening assays covering metabolic stability, enzyme inhibition and induction, alongside supporting clients in designing and interpreting DDI studies to support regulatory submission, supporting R&D and bespoke studies and driving continuous improvement projects.

Watch the webinar to learn more!

[hs-form id="f0365c7a-f5d3-411a-a11b-097b618db7a5" show="hide on login" url="https://news.evotecsciencepool.com/hubfs/Sciencepool/Videos%20and%20Webinars/Cyprotex%20webinars%20and%20videos/cyp-induction-webcast-on-demand-july2022.mp4"]

Tags: Videos & Webinars, ADME/DMPK

EVOiR&D: An integrated discovery and development platform to deliver best-in-class biologics at Evotec

Posted by Evotec on Jun 27, 2022 4:36:27 PM

About the Webinar

This is a recorded live presentation given by Thierry Wurch, PhD - Senior VP, Integrated Biologics Discovery at Evotec during the Antibody Engineering and Therapeutics Europe (AE&T) conference in Amsterdam, June 2022.

Content Summary:
  • At Evotec we discover, develop and manufacture novel medicines for hard-to-treat diseases through efficient partnerships with academia, biotechs and pharma
  • For antibody-based modalities, Evotec has developed an integrated discovery platform ranging from target validation, antibody discovery and optimization, in vitro/in vivo pharmacology, PK, and toxicology to select the best clinical candidates
  • We apply both humanized, mouse-derived hybridoma and phage display (from immune and synthetic antibody libraries) coupled to automated HTS antibody screening and AI/ML-based optimization, antibody hits are selected to best fit their intended modality, (e.g. mAbs, ADCs, bispecifics)
  • A particular emphasis is placed on integrating good manufacturing properties for the selected antibody sequence

 


About the Speaker

 

Wurch,ThierrySquare

Thierry Wurch

SVP, Integrated Biologics Discovery | Evotec

Thierry joined Evotec in May 2022 as SVP Integrated Biologics Discovery. He has more than 22 years of expertise in the antibody R&D space primarily in Oncology and immune-oncology. Thierry held positions of growing strategic importance from head of an antibody discovery and engineering department (Pierre Fabre, 2003-2011), head of immunotherapy discovery research activities (Servier, 2011-2017) then moving to BD-oriented activities and heading external innovation for Oncology (Servier, 2017-2020 and Ipsen 2020-2022). Thierry is also Chairman of the antibody sub-committee at NC-IUPHAR, member of the Editorial board of mAbs Journal and Distinguished Advisor of The Antibody Society.

 

[hs-form id="052874a9-75e5-4960-9b82-931f9dd753b7" show="hide on login" url="https://player.vimeo.com/video/719092289"]

Tags: Presentations, Videos & Webinars, Biologics

Translate Your Idea Into Product: AI-Driven Antibody Discovery at Evotec

Posted by Evotec on Apr 21, 2022 12:41:44 PM

Monoclonal antibodies (mAbs) have been a huge success story in the biopharmaceutical industry. They have changed the landscape of biologicals and offered therapies for previously untreatable diseases. Although mAbs have been on the market since the mid 1980s, they have become increasingly sophisticated over the past decades. This also holds true for the technologies enabling the identification, design, preclinical and manufacturing processes of monoclonal antibodies.

While the traditional hybridoma technology is still broadly used for the creation of mAbs, novel technologies such as immune antibody libraries or fully humanoid antibody libraries have emerged in recent years. Moreover, researchers can today leverage a range of powerful approaches to optimize the mAb creation process, e.g., high-throughput screening, state-of-the-art sequencing, AI / machine learning or analytics. This, in turn, speeds up the development cycle, allows for precise selection of the desired mAb properties and ultimately reduces failures of monoclonal antibodies at advanced development stages.

But how to choose from the vast range of technologies for antibody development? This challenge was discussed at Evotec´s recent Innovation Week in a session titled "Translate your idea into a product: AI -driven antibody discovery at Evotec".

The session covered Evotec´s capabilities for supporting all activities across the R&D continuum, i.e.

  • Discovery and optimization of novel antibodies for specific disease targets,
  • Evaluation of lead antibodies for disease efficacy and safety and
  • Process development and manufacturing.

"In many cases, it is not the question of using either one or another technology," says Barbara Bachler-Konetzki, Group Leader In Vitro Pharmacology at Evotec. "Depending on the desired properties of the monoclonal antibody, combining several technologies will do the trick. Therefore, it is important to have access to a comprehensive repertoire of leading-edge, synergistic technologies."

For state-of-the-art monoclonal antibody development, Evotec has established a unique one-stop-shop from target identification to IND. This includes a broad technology platform as well as unparalleled expertise in drug development and even manufacturing, including latest advances in artificial intelligence and machine learning such as generative adversarial networks (GAN) to create synthetic realistic outcomes by machine learning (J.HAL).


The resulting integrated biologics platform is called J.DESIGN and integrates molecular, process and manufacturing design.


The example of Evotec´s internal SARS-CoV-2 campaign shows how its proprietary J.HAL technology can be used to identify antibodies effectively blocking the SARS-CoV-2 infection pathway by binding to SARS spike protein, effectively neutralizing the infectivity across several SARS-CoV-2 strains. The subsequent in silico sequence analysis informs about mAb properties and engineering opportunities to reach the desired properties re immunogenicity, stability etc. Further steps, e.g., sequence and stability optimization, improve manufacturability and yields or pharmacokinetics (PK).


For mAb development, Evotec pursues a translational approach, i.e., leveraging its extensive expertise in various therapeutic areas to facilitate the setup of disease-relevant biological assays. Among others, this allows for PK/PD characterization of biologics early in the R&D process as well as the prediction of downstream in vivo efficacy and demonstration of target engagement. Moreover, Evotec’s pre-clinical department offers the full range of in vitro and in vivo GLP and non-GLP pre-clinical evaluation studies to assess the safety profile of the drug candidate. In addition, Evotec has established several sophisticated manufacturing facilities worldwide to reduce the risk of downstream attrition and delay.


This unparalleled infrastructure and translational expertise put Evotec in a unique position to conduct leading-edge, integrated monoclonal antibody development programs all the way from target identification to manufacturing.

FULL REPLAY

Tags: Blog, Videos & Webinars, Biologics

Prepared for Viruses and More....

Posted by Evotec on Apr 14, 2022 5:41:39 PM

About this Webinar

In this short recording, Dr Pia Thommes, VP Anti-Infectives and Virology Therapeutic Leader discusses:

  • Current challenges in Infectious Diseases drug discovery
  • Human SARS-CoV-2 and other emerging viruses
  • Industry relevant in vivo models
  • The wider reaching consequences of the COVID pandemic

More about Dr Pia Thommes.

Pia Thommes border

Pia gained her PhD in Molecular Genetics and followed this with a postdoctoral in biochemistry, focusing on DNA replication and cell cycle. She has 12 years experience in drug discovery of antivirals at GW/GSK, 4 years work in oncology on DNA Damage Response at KuDOS/ AZ. In 2012 Pia took on a role as Scientific Operations Director at Euprotec, a specialist CRO for infectious disease, this was incorporated into the Evotec family in 2014. Currently Pia is working as VP of Anti-infectives in Alderley Park and also Therapeutic Area Lead for Virology.

Hope you enjoy the webinar

Watch the Recording Now

Tags: Videos & Webinars, In vivo Pharmacology, Anti-Infectives

AAV Gene Therapy: Closing the Translational Gap

Posted by Evotec on Mar 31, 2022 10:26:55 AM

About the Webinar

This exciting collaboration between Evotec and Professor Dirk Grimm from the University of Heidelberg will review the current challenges facing the field of gene therapy.

The webinar includes:

  • A short introduction to AAV gene therapy
  • Recent clinical findings
  • Lessons we have already learned regarding improving AAV-based gene therapies
  • Strategies for next generation canidates
  • Efficacy and safety evaluation in preclinical models and their translatability into humans

 


About the Speakers

 

WernerHöllriegl

Werner Höllriegl

VP, Head of In Vivo Gene Therapy | Evotec

Werner Höllriegl is heading In Vivo Gene Therapy at Evotec GT in Orth an der Donau, Austria. He received his degree in Veterinary Medicine from the University of Veterinary Medicine Vienna, Austria. After spending a couple of years as Assistant Professor at the Department of Anesthesiology, he moved into industrial research spending more than 15 years in different Pharma Companies (Baxter, AstraZeneca, Novartis Institutes for BioMedical Research, Baxalta, Shire, Takeda) in Research and Nonclinical Development, focussing on biologics and in vivo gene therapy.

HanspeterRottensteiner_evotec

Hanspeter Rottensteiner

VP, Head of In Vitro Gene Therapy | Evotec

Hanspeter Rottensteiner is heading In Vitro Gene Therapy at Evotec GT in Austria. Biochemist by training, Hanspeter has more than 10 years in academia, and 15 years of experience in Pharma (Baxter, Takeda) in senior positions. He brings significant expertise in drug development of biologics and gene therapies, with a strong focus on rare diseases. He received his degree in Biochemistry from the University of Vienna, Austria.

 

Rudiger

Rüdiger Fritsch

Principle Scientist, Metabolic Disease | Evotec

Rüdiger Fritsch is heading a transcriptomics team at Evotec. He has recieved his PhD from the Max Planck Institute for Biophysical Chemistry. With over 15 years of experience as a biologist, Rüdiger has a strong expertise in omics.

 

Dirk Grimm

Dirk Grimm

Professor of Viral Vector Technologies Medical Faculty and the Department of Infectious Diseases/Virology | Heidelberg University

Dirk Grimm is heading the "Virus-host interactions" research group within the Department of Infectious Diseases/Virology. He has over 25 years of experience in AAV capsid and genome engineering as well as  in human gene therapy. Dirk has trained under AAV experts Jürgen Kleinschmidt (German Cancer Research Center Heidelberg) and Mark Kay (Stanford University School of Medicine). 

Watch the webinar to learn more!

[hs-form id="6827abd7-94a5-4df5-8beb-3d1da436ad90" show="hide on login" url="https://news.evotecsciencepool.com/hubfs/Webinars/AAV%20GENE%20THERAPY_2022/AAV%20Gene%20Therapy%20Webinar%20WoD.mp4"]

Tags: Videos & Webinars, ADME/DMPK, Modelling and Simulation

RNA-Based Medicine: Expanding the Druggable Target Space to RNA

Posted by Evotec on Mar 29, 2022 1:10:45 PM

While the public has taken note of RNA-based medicine only with the advent of mRNA-based Corona virus vaccines, biopharmaceutical research and development has been working on mRNA-based medicine for almost two decades. Evotec also expanded the druggable target space to RNA and in the last years added considerable know-how in RNA-based medicine.

RNA is used by cells in multiple ways: mRNA is conveying genetic information from DNA to the ribosomes which also are made from RNA (ribosomal RNA), where another RNA species (tRNA) is transporting amino acids to the ribosomal apparatus so that a protein can be synthesized. In addition to mRNA, there are also shorter RNA molecules being used in the cell for the regulation of genes and entire genetic cascades.

This provides for plenty of potential interventions: antisense (ASO) and short interfering RNA (siRNA) can up or down regulate an RNA target, e.g., to block the translation of an unwanted or diseased protein or to suppress or stimulate the expression of genes. RNA can be targeted with (complementary) RNA, but it is also possible to alter or block the translation, re-locate or initiate RNA, degradation, etc. by small molecules interfering with the three-dimensional structure of RNAs or protein-RNA-complexes.

During our recent Innovation Week, Evotec experts Steffen Grimm, Group Leader, Hit ID & Biophysics, and Hilary Brooks, Senior Research Scientist, In Vitro Pharmacology, hosted a session called "The early bird catches the helix: Expanding the druggable target space to RNA".

In the session, they discussed how to:

  • Expand the potential for drugs targeting RNA to offer alternative solutions for diseases with otherwise undrugged targets
  • Target RNA providing highly specific solutions for protein removal, alternative splicing or pathway regulation via noncoding RNA
  • Use the small molecule RNA targeting platform to contribute to new opportunities for target identification and validation

RNA as Therapeutics
Using RNA as therapeutics is not trivial. Nucleic acids introduced from outside may trigger adverse reactions by the innate immune system. A lot of knowledge is necessary to ensure delivery, avoid degradation and inflammation and to fine-tune the stability and function of the molecules. RNA may also have off-target effects. To ensure efficacy and safety, monitoring these early on needs to be incorporated into the developmental workflow. High quality synthetic RNA is costly to make, therefore a scaleable process and the relevant analytics must be established early in the process to accompany both the discovery and development stages of research with quality test material; Eventually producing GMP grade RNA at a commercial scale (several hundred grams) for human administration.

Evotec already has integrated all capabilities under one roof, allowing for the complete preclinical data set, reduced transition times and efficient communication to the regulators. For antisense oligonucleotide therapy, efficient hit sequences that knock down target expression can be selected in a matter of weeks. Toxicity profiling is a priority to establishing final leads and, subsequently, project-specific dose, duration and delivery will be established using optimized backbone chemistry. Using its in-silico capabilities as well as iPSCs, animal models, transcriptomics, etc. Evotec is able to predict toxicity and efficacy, and de-risk unwanted immune stimulation as well as off-target effects. For manufacturing, Evotec is discovery-capable and already building medium-scale capacity (up to 50g) which will be ready by 2023.

For inhibiting the translational machinery, Evotec has established an RNA small molecule targeting platform and established in various case studies, molecules binding to RNA, and demonstrating a significant effect in vitro without affecting cell viability. Evotec’s capabilities also allow the creation of a representation of the 3-dimensional structure of the target complex and its interaction with the compounds.

Evotec’s experienced team of scientists with proven drug discovery and development expertise already have a track record of driving RNA targeting projects forward. Its integrated medicinal and computational chemistry capabilities, combined with bioinformatics, structural biology, pharmacology, and drug safety expertise allows for the identification and characterization of RNA target species and their modulation by different modalities. Partner projects can be driven all the way from target identification to IND and beyond. Evotec therefore is a low-risk outsourcing partner and a company continually investing in its platform to the benefit of the customer.

LEARN MORE

Tags: Oncology, Blog, Videos & Webinars, Hit & Target ID/Validation, In vitro Biology, IND Enabling Studies/Preclinical Development, In vivo Pharmacology