Ellen Capon (Drug Target Review)

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    Article

    How MMR-deficient colorectal cancers regulate their growth

    2024-07-09T10:00:17

    Understanding how MMR-deficient colorectal cancers drive tumour growth and avoid immune detection could pave the way for personalised cancer medicine.

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    Article

    Changing the paradigm of drug discovery processes with AI

    2024-06-25T10:00:16

    We had the privilege of speaking to Cellarity’s CEO, Fabrice Chouraqui, about how the company is leveraging AI to completely revolutionise the drug discovery process and unlock treatments for a vast array of diseases, even in the absence of known targets.

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    Article

    The evolution of cell therapy to address unmet medical needs

    2024-06-19T10:00:55

    We had the privilege of interviewing Brian Culley, CEO of Lineage Cell Therapeutics. He discusses how Lineage’s pluripotent stem cell platform is extraordinarily advantageous, details two early-stage programmes addressing auditory and vision disorders and reveals how Lineage is choosing to target conditions that will make a real difference.

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    Article

    Tessera Therapeutics: addressing Alpha-1 Antitrypsin Deficiency

    2024-06-18T10:00:30

    As the industry looks beyond CRISPR to safely introduce therapeutic genomic changes anywhere in the body, in vivo gene editing holds immense potential to address diseases with a genetic basis. Boston-based biotech Tessera Therapeutics is pioneering the next generation of genetic medicines with its Gene Writing™ platform. At this year’s ...

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    Article

    New algorithm forms atlas of histomorphological phenotypes

    2024-06-13T15:30:23

    The algorithm can accurately diagnose cases of lung adenocarcinoma, determining structural features that are statistically most significant for assessing disease severity and likelihood of tumour recurrence.

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    Article

    The promise of vectors targeting the LDL receptor

    2024-06-04T10:00:57

    In this Q&A, Pascaline Lécorché, Head of Chemical Biology at Vect-Horus, outlines the potential of RNA interference therapeutics and the challenges of their use in vivo. There are several strategies to overcome these, and why peptide-based vectors targeting the LDL receptor are a promising approach.

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    Article

    Treating immune-mediated diseases with nanoparticles

    2024-06-03T10:00:08

    In this Q&A, we had the privilege of speaking to COUR Pharmaceuticals’ CEO John Puisis. He offers insights into how their innovative immune-modifying nanoparticle platform differs from traditional approaches for treating immune-mediated diseases.

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    Article

    Harnessing natural killer cells to combat age-related diseases

    2024-05-28T10:00:45

    In this Q&A, Celularity’s CEO and founder Dr Robert Hariri details the preclinical research that indicates that placenta-derived unmodified NK cells and genetically modified NK cells can target and selectively eliminate cells expressing stress ligands.

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    Article

    Leveraging ADCs in precision oncology strategy

    2024-05-27T10:00:58

    In this Q&A, senior leaders at Caris Life Sciences discuss how the company is advancing precision medicine by integrating ADCs into patient-specific cancer treatment plans, focusing on novel target discovery through comprehensive molecular profiling and clinico-genomic data.

  • Nina Weisser
    Article

    Improving treatment responses to solid tumours with trispecific TCEs

    2024-05-23T10:00:11

    Following Zymeworks’ presentation at AACR 2024, in this Q&A, Dr Nina Weisser explains how the next generation trispecific T cell engager platform with integrated CD28 costimulation is engineered to tackle solid tumours.

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    Article

    Enhancing gene therapy with Circio

    2024-05-22T10:00:02

    In this Q&A, Erik Wiklund, CEO of Circio, explains the key findings of their circVec circular RNA platform technology, why they chose AAV-based gene therapy for AATD as the lead programme, and their plans for the future to enhance the potency and reduce the cost of current gold-standard gene therapy.

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    Article

    Utilising engineered peptides for immunotherapy

    2024-05-14T10:00:11

    In this Q&A, Dr DaeYong Lee discusses how a new method for building up natural immune response could lead to new immunotherapy drugs with safer toxicity profiles.

  • Luke Piggott Heashot
    Article

    Biomarker identification in the realm of rare diseases

    2024-05-07T10:00:19

    In this Q&A, Debiopharm’s Principal Scientist Dr Luke Piggott defines the critical requirement of biomarkers for identifying rare diseases. He illuminates how AI-enhanced approaches are accelerating the drug discovery process, particularly regarding clinical trial enrolment, and the breakthroughs he hopes to see in the future.

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    Uncovering the genetic and cellular impacts of smoking

    2024-04-25T10:00:46

    Epigenetic data assessing the effects of smoking on DNA methylation could serve as biomarkers of exposure effects.

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    Developing the next generation of antibody drug conjugates

    2024-04-22T10:00:17

    In this Q&A, Léo Marx, Medicinal Chemistry Project Manager at Debiopharm, details how the therapeutic window of ADCs can be impacted, how we can overcome the challenges associated with achieving site-specific bioconjugation, and other essential considerations for optimising ADC performance.

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    Pioneering the advancement of pre-targeted radioimmunotherapies

    2024-04-16T10:00:03

    Although pre-targeting is still in its infancy, it has immense potential to increase state-of-the-art radioligand therapies. In this Q&A, PreTT reveals how their pre-targeted RLTs surpass traditional methods, transforming cancer treatment.

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    Identifying vascular disease associations

    2024-04-11T10:00:52

    In this Q&A, Associate Professor Dr Mete Civelek shares insights from the University of Virginia’s exciting recent study identifying several potential therapeutic targets for accelerating translational research in cardiovascular disease treatment, with a focus on proteins associated with the extracellular matrix (ECM) secretion by smooth muscle cells (SMCs).

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    HIF inhibition: a potential therapeutic approach for cancers

    2024-04-10T10:00:13

    In this Q&A, Curve Therapeutic’s Chief Scientific Officer Professor Ali Tavassoli discusses how dual HIF inhibition could combat solid tumours.

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    How nucleolar stress accelerates aging in mice

    2024-04-09T10:00:26

    Dr Fernández-Capetillo shares his insights from a recent study conducted at the CNIO, elucidating how the expression of (PR)arginine-rich peptides affects ribosomal protein translation and accumulation, and how accelerated aging can be alleviated.

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    Using AI to predict metastatic behaviour of NSCLC

    2024-04-08T10:00:07

    Dr Richard Cote and Dr Ramaswamy Govindan of the Washington University School of Medicine elucidate how AI, particularly deep learning networks, could identify histopathologic features in non-small cell lung cancer, and impact the treatment approach for early-stage patients.

More by Ellen Capon (Drug Target Review)