Base to Base Biotech

Jim Cornall

The Base to Base Biotech podcast is a weekly look at what's happening in the world of biotech, with interviews with biotech leaders around the world. Whether it's a new drug, cutting-edge technology, product launches, new technology, major finding announcement or clinical trial results, Base to Base Biotech keeps you informed. The podcast is hosted by former biotech editor and broadcaster, the award-winning media veteran Jim Cornall. Base to Base is an Ayr Coastal Media Ltd production.

  1. Base to Base biotech podcast 50: Drugs for kidney transplants, glycans, and drug delivery

    1D AGO

    Base to Base biotech podcast 50: Drugs for kidney transplants, glycans, and drug delivery

    As this week’s podcast comes hot on the heels of International Women’s Day and World Kidney Day, which was yesterday, we’ve been able to squeeze them both in. The conversations this week are with Hansa Biopharma CEO Renée Aguiar-Lucander, about imlifidase for kidney transplant patients; Kyron.bio CEO Emilia McLaughlin, about glycosylation; and hydrogel-based drug delivery solutions company AmacaThera’s CEO, Mike Cooke. Times: 03:56 Kyron.bio 19:14 AmacaThera 43:01 Hansa Biopharma Hansa Biopharma Hansa Biopharma AB is set for a busy year. In December, the Food and Drug Administration (FDA) has notified the company that the previously accepted Biologics License Application (BLA) for imlifidase has been assigned a Prescription Drug User Fee Act (PDUFA) action date of December 19, 2026. Imlifidase is conditionally approved in the EU, Norway, Liechtenstein, Iceland and the UK under the tradename IDEFIRIX for the desensitisation treatment of highly sensitised adult kidney transplant patients with a positive crossmatch against an available deceased donor. IDEFIRIX is also approved in Australia and Switzerland. The company also has HNSA-5487, a next-generation IgG-cleaving molecule being developed for Guillain-Barré Syndrome (GBS). Kyron.bio French biotech company Kyron.bio and pharma company Servier recently announced a partnership to advance precision glycosylation in antibody therapeutics. The partnership underlines the two companies’ vision to unlock the potential of glycans in next-generation biologics design to deliver safer and more effective therapeutics for patients Kyron.bio’s glycobiology platform aims at enhancing the efficacy, safety, and scalability of next-generation antibody therapeutics across multiple disease areas. To date, engineering of glycans have been under-exploited, due to technical challenges, limiting the use of glycan engineering in drug design. AmacaThera AmacaThera is a developer of next-generation hydrogel-based drug delivery solutions. Using a blend of known polymers, AmacaThera’s clinically validated hydrogel platform is transforming drug delivery by enabling the precise, tunable, and sustained release of a range of therapeutics, from small molecules to biologics. Transforming from liquid to gel at body temperature, AmacaThera’s hydrogel enables drugs to be delivered to and stay where they are needed and released over days or weeks, depending on the specific needs of each therapeutic application. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    1h 12m
  2. Base to Base biotech podcast 49: Gene therapy for kidney disease, and using AI to transform diagnostics

    MAR 6

    Base to Base biotech podcast 49: Gene therapy for kidney disease, and using AI to transform diagnostics

    This week, we’re chatting with Haseeb Ahmad, CEO of Purespring Therapeutics, about gene therapies in kidney disease, and with Pahini Pandya, Panakeia CEO, about colorectal cancer biomarkers, the potential of AI in clinical decision-making and how AI can transform workflows in diagnostics. Times: 03:34 Purespring 24:11 Panakeia Technologies Purespring Therapeutics Purespring is a precision nephrology company pioneering first-in-class, targeted genetic therapies designed to preserve kidney function. The company is focused on transforming the treatment of kidney disease—an area of enormous unmet need, with more than 840m people worldwide living with chronic kidney disease. Purespring’s lead programme, PS-002, for IgA nephropathy (IgAN) is set to enter the clinic this quarter. It marks the first podocyte-targeted gene therapy to reach clinical development and offers a highly differentiated approach compared with other emerging treatments, including those from Vertex and Otsuka. Panakeia Technologies Panakeia Technologies recently published a real-world clinical validation showing that AI can determine critical colorectal cancer biomarkers in minutes, in a test across 1,243 patients and 3,576 images in NHS hospitals. While not yet used directly in patient care, the study demonstrates the potential for AI to support clinical decision-making, reduce lab bottlenecks, and help clinicians act faster — a topic highly relevant to the goals of the UK government's cancer plan and the ongoing discussion around innovation in healthcare. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    52 min
  3. Base to Base biotech podcast 48: GPCRs and beating neurodegenerative diseases

    FEB 27

    Base to Base biotech podcast 48: GPCRs and beating neurodegenerative diseases

    The conversations on this week’s podcast are with CEO of Merz Therapeutics, Stefan König, about a variety of neurodegenerative conditions and a botulinum neurotoxin, and with CEO of Kainova Therapeutics, Sean MacDonald, about – among other things – G-protein coupled receptors, or GPCRs. Times: 03:21 Merz Therapeutics 30:34 Kainova Therapeutics Kainova Therapeutics Kainova Therapeutics is a clinical-stage biopharmaceutical company headquartered in Montreal, Canada. The company develops drug candidates targeting GPCRs, with programmes focused on immuno-oncology and inflammatory diseases. The company’s pipeline includes antibody and small-molecule programmes directed at GPCR targets. These include a CCR8-targeting antibody programme being evaluated in oncology, as well as PAR2 and EP4 antagonist programmes with potential applications in inflammatory conditions. Its development activities span preclinical and early clinical stages. Kainova was previously known as Domain Therapeutics. Merz Therapeutics Merz Therapeutics is a pharmaceutical company headquartered in Frankfurt, Germany. It operates as the therapeutics arm of the Merz Group and focuses on the development and commercialisation of medicines for neurological and neuro-related conditions. The company’s portfolio includes treatments used in areas such as movement disorders, spasticity and other neurological conditions. Merz Therapeutics also engages in focused acquisitions and partnerships to broaden its portfolio and reach more patients globally. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    53 min
  4. Base to Base biotech podcast 47: Accurate prostate cancer diagnosis and ocular gene therapy

    FEB 20

    Base to Base biotech podcast 47: Accurate prostate cancer diagnosis and ocular gene therapy

    The conversations on this week’s podcast focus on a rapid and accurate prostate cancer diagnostic test, with Valley Diagnostics’ CEO Dave Taylor; and on gene therapy for retinal disease, with Lance Baldo, CEO of Beacon Therapeutics. Times: 03:12 Beacon Therapeutics 27:38 Valley Diagnostics Valley Diagnostics Valley Diagnostics is a Welsh company developing next‑generation lateral flow diagnostic tests designed for early detection of human and animal diseases. Their approach uses patented biomarkers to make faster and more accurate screening possible in GP surgeries, point‑of‑care settings, and at home. Their current pipeline includes tests for prostate cancer, lung cancer, and bovine tuberculosis. The company is working with academic and clinical partners across Wales and England to validate its biomarkers through large‑scale studies. One example is the OSCAR clinical study, which is screening thousands of urine samples to support development of a rapid prostate cancer test. In recent weeks, Valley Diagnostics signed several licensing agreements with Aberystwyth University, securing exclusive global rights to biomarker IP across four major disease areas. These agreements are intended to support commercialisation of their point‑of‑care tests and move them toward market readiness. Beacon Therapeutics Beacon Therapeutics is an ocular gene therapy company focused on inherited retinal diseases, including X‑linked retinitis pigmentosa (XLRP). Earlier this month, the company announced it had raised over $75m in an oversubscribed Series C financing led by Life Sciences at Goldman Sachs Alternatives and with participation from the Retinal Degeneration Fund (RD Fund), the venture arm of Foundation Fighting Blindness. The new funds will be used to complete the development of lead programme, laru-zova, a potential best-in-class gene therapy currently being investigated for the treatment of patients with XLRP, and progress commercialisation plans. The funds will also be used to help support the development of Beacon’s pipeline candidates for geographic atrophy, as well as an inherited cone rod dystrophy, and another undisclosed asset. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    1h 1m
  5. Base to Base biotech podcast 46: Endometriosis and closing care gaps

    FEB 13

    Base to Base biotech podcast 46: Endometriosis and closing care gaps

    The conversations on this week’s podcast are with Vibhor Gupta, director and founder of Pangaea Data, and endogene.bio CEO María Teresa Pérez Zaballos. Times: 03:09 Pangaea Data 23:43 endogene.bio Endogene.bio endogene.bio is a precision medicine company based in France developing a non-invasive diagnostic for endometriosis. The company’s aim is to apply precision medicine to female health. The company was formed in 2022 by Maria Teresa Perez Zaballos and Cristina Fernandez Molina. Its innovations include a non-invasive diagnostic approach that uses menstrual blood rather than traditional blood draws or invasive surgery. By focusing on the uterine environment directly, the company aims to replace the current "gold standard" of laparoscopic surgery with a high-signal "liquid biopsy" that can be collected at home. The company recently published a preprint, “Beyond one-size-fits-all: single-cell transcriptomic signatures predict drug efficacy and reveal responder subgroups in endometriosis.” The company’s most recent scientific output, it was published in January 2026, and shows how the company uses single-cell transcriptomic signatures to map the molecular heterogeneity of the disease. The research has identified distinct "responder subgroups," suggesting that endometriosis is not a single condition but a collection of cellular programmes that dictate how a patient will react to specific therapies. This primary data positions endogene.bio’s platform as both a diagnostic tool and a predictive framework for patient stratification in clinical trials, aiming to move the field toward personalized treatment selection. Pangaea Data Pangaea Data provides a clinical-grade AI platform, PALLUX, designed to identify untreated, misdiagnosed, and under-treated patients by extracting intelligence from unstructured records. The platform emulates clinical reasoning to scan doctors’ notes and pathology reports, identifying care gaps across conditions such as oncology, rare diseases, and chronic kidney disease. It operates behind the healthcare organisation's firewall to ensure data privacy while integrating directly into existing EHR workflows and ambient listening tools. The platform's "Privacy by Design" architecture allows it to scale across multiple disease areas without the need for manual data labelling. By mapping clinical features and disease trajectories, PALLUX provides clinicians with a single dashboard to access actionable insights. The methodology is currently deployed across 13 countries, helping pharmaceutical companies and healthcare providers discover up to five times more patients who would otherwise be missed by conventional search methods. In December 2025, the London-headquartered company announced a multi-year strategic collaboration with AstraZeneca to advance precision healthcare through multimodal AI. The collaboration focuses on co-developing an enterprise-grade platform that fuses clinical, imaging, and genomic data to improve real-time treatment recommendations and speed up clinical trial recruitment. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    48 min
  6. Base to Base biotech podcast 45: Chronic pain, urology, Affibody molecules and radioligand therapy

    FEB 6

    Base to Base biotech podcast 45: Chronic pain, urology, Affibody molecules and radioligand therapy

    This week, we chat with Affibody CEO David Bejker, and Martin Gleave, founder and chief medical officer at Sustained Therapeutics. Times: 03:47 Affibody 23:28 Sustained Therapeutics Sustained Therapeutics A spin-out from the University of British Columbia in Canada, Sustained Therapeutics utilises a proprietary polymer gel technology to develop locally injected, long-acting medications. The platform is designed to release active pharmaceutical ingredients in a controlled manner over several weeks, aiming to replace traditional oral delivery or frequent injections. While the primary focus is on managing acute and chronic pain without the use of opioids, the company is also exploring applications for the technology in inflammatory diseases and urology. The core of the company’s pipeline involves a non-addictive, sustained-release formulation that targets the site of pain directly. By providing localized treatment, the technology seeks to minimize systemic side effects and reduce the patient's reliance on addictive substances. Beyond pain management, the firm is adapting its delivery system for oncological use, specifically targeting upper tract urothelial carcinoma, where localized, prolonged drug exposure is clinically advantageous. In January 2026, the company reported positive data from its phase II clinical trial for a long-acting non-opioid medication designed for chronic pain. The results indicated that the sustained-release mechanism effectively extended pain relief while maintaining a favourable safety profile. These findings support the continued expansion of their clinical program into other chronic pain indications, including pelvic and scrotal pain, which are slated for further study throughout the year. Affibody Affibody, a Swedish clinical-stage biopharmaceutical firm, is developing a new class of small proteins known as Affibody molecules. These engineered proteins are significantly smaller than traditional monoclonal antibodies—roughly one-tenth the size—which allows for better tissue penetration and flexible formatting for multi-specific treatments. The company’s research spans two main pillars: immunology and radiopharmaceuticals, leveraging its library of more than 10bn unique protein sequences to identify highly specific binders for various disease targets. Recent activity has centred on a significant financial and clinical milestone. In late January 2026, the company launched a $29m rights issue, fully guaranteed by its lead shareholder, to fund its expanding radiopharmaceutical pipeline. This capital injection follows successful early-stage data for its RLT candidate, ABY-271; a Trial Review Committee recently recommended advancing the candidate to the second part of a phase I study in HER2-positive metastatic breast cancer after initial patient cohorts showed promising safety and biodistribution. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    45 min
  7. Base to Base biotech podcast 44: Treating breast cancer and how a CDMO and immun0-oncology company collaborate

    JAN 30

    Base to Base biotech podcast 44: Treating breast cancer and how a CDMO and immun0-oncology company collaborate

    This week, we chat with Pan Cancer T CEO Dr. Rachel Abbott, about – among other things – triple-negative breast cancer. We also have a conversation with Erik Manting, CEO of immunotherapy company Mendus, and Janet Hoogstraate, CEO of the CDMO helping them, North X Biologics. Times: 03:56 Pan Cancer T 20:23 Mendus/NorthX Biologics Mendus Mendus is a Swedish–Dutch immuno-oncology company developing cell-based therapies aimed at stopping cancers from coming back rather than treating only the initial tumour. Its lead product, vididencel, is an off‑the‑shelf dendritic cell vaccine being developed as a post‑remission therapy for patients with acute myeloid leukaemia (AML), and more recently chronic myeloid leukaemia, who remain at high risk of relapse after standard treatment. Mendus’ pipeline explores how active immunotherapies could extend treatment‑free survival in different myeloid malignancies. In 2025, Mendus refined its strategy for vididencel on the back of positive data from a phase 2a trial in high‑risk AML, where long‑term follow‑up has shown durable remissions and an encouraging safety profile. Vididencel is also being studied in a phase 2b trial in combination with oral azacitidine, aimed at broadening its use beyond patients with measurable residual disease. NorthX Biologics North X Biologics is a contract development and manufacturing organisation (CDMO) and national innovation hub for complex biologics in Sweden. The company provides GMP‑grade development and manufacturing services for plasmid DNA, recombinant proteins, viral vectors, and cell & gene therapies from its facilities in Matfors and on the Karolinska University Hospital campus in Stockholm. Its goal is to give emerging biotechs and academic groups access to infrastructure and regulatory expertise that would be hard to build alone. NorthX has expanded into cell therapy manufacturing, adding capabilities for multiple cell types, including pluripotent stem cells. The organisation aims to strengthen Sweden’s role as a European centre for advanced therapy medicinal products (ATMPs). NorthX has collaborated with Mendus since 2023. In late 2025, they announced successful GMP manufacturing certification for vididencel at NorthX’s facilities, which supports Mendus’ upcoming late‑stage clinical trials and eventual commercial supply. Pan Cancer T Pan Cancer T brings a different angle to cancer immunotherapy, focusing on engineered T cell receptor (TCR‑T) therapies for hard‑to‑treat solid tumours. Based in Rotterdam and spun out from Erasmus MC in 2020, the company is building a pipeline around tumour‑specific antigens that are consistently and strongly expressed across multiple cancers. Its lead programme, PCT1:CO‑STIM, is being developed for women with triple‑negative breast cancer, an aggressive form of the disease with limited treatment options and poor survival once it has spread. By focusing on shared antigens across different tumour types, Pan Cancer T aims to develop treatments that could, in time, be applied beyond breast cancer to other solid tumours including melanoma and cancers of the skin, colorectum, stomach, oesophagus, ovary and uterus. In December 2025, the company announced €10m financing to move PCT1:CO‑STIM into its first‑in‑human clinical trial in the Netherlands. To get in touch with guest suggestions, or to advertise on the podcast, contactjim@deeptechdigest.com

    47 min
  8. Base to Base biotech podcast 43: Natural killer cell therapy and attacking tumours

    JAN 23

    Base to Base biotech podcast 43: Natural killer cell therapy and attacking tumours

    This week, we have a conversation with Lisa Guerrettaz, executive director, Pharmacology and Translational Science at Artiva Biotherapeutics; and Avacta Therapeutics’ CEO Christina Coughlin. Times: 04:12 Artiva Biotherapeutics 21:30 Avacta Therapeutics Artiva Biotherapeutics Artiva Biotherapeutics is a clinical‑stage cell therapy company developing off‑the‑shelf (allogeneic) natural killer (NK) cell therapies for autoimmune diseases and cancer. Headquartered in San Diego and founded in 2019, the company was created as a spin‑out from GC Cell (formerly GC Lab Cell) in South Korea, alongside a strategic partnership granting Artiva exclusive rights (outside Asia, Australia and New Zealand) to GC Cell’s NK manufacturing technology and associated programmes.​ Artiva’s lead programme is AlloNK, a non‑genetically modified, cryopreserved NK cell therapy designed to enhance antibody‑dependent cellular cytotoxicity (ADCC) when paired with monoclonal antibodies. The company positions this approach to achieve deep B‑cell depletion in outpatient settings without the complexity and cost associated with bespoke autologous cell therapies.​ In terms of clinical activity, AlloNK is being evaluated across three ongoing trials in B‑cell‑driven autoimmune diseases, including company‑sponsored and investigator‑initiated basket studies covering indications such as rheumatoid arthritis, systemic lupus erythematosus, lupus nephritis and Sjögren’s disease. Artiva has treated more than 100 patients with AlloNK across oncology and autoimmune disease and is planning FDA interactions in the first half of 2026 aimed at enabling a pivotal trial pathway in rheumatoid arthritis. Avacta Therapeutics Avacta is a life sciences company best known for its Affimer platform—engineered binding proteins positioned as an alternative to antibodies for use in diagnostics, reagents and therapeutics. ​ The company’s activities span both life science reagents/diagnostics and oncology therapeutics, with the latter centred on its pre|CISION technology, which is designed to activate drugs selectively in the tumour microenvironment. ​ In therapeutics, Avacta’s most advanced programme is faridoxorubicin (AVA6000), which uses a fibroblast activation protein (FAP)‑targeted mechanism intended to release an active form of doxorubicin preferentially at tumour sites. The programme has moved into phase 1b expansion cohorts to assess efficacy in more homogeneous patient populations and help guide expectations for later‑stage studies.​ Earlier this month, the company announced U.S. Food and Drug Administration (FDA) clearance of the Investigational New Drug (IND) application for its FAP-Exd programme, the first pre|CISION peptide drug conjugate based on the highly potent topoisomerase I inhibitor, exatecan. To get in touch with guest suggestions, or to sponsor or advertise on the podcast, please email jim@deeptechdigest.com

    50 min

About

The Base to Base Biotech podcast is a weekly look at what's happening in the world of biotech, with interviews with biotech leaders around the world. Whether it's a new drug, cutting-edge technology, product launches, new technology, major finding announcement or clinical trial results, Base to Base Biotech keeps you informed. The podcast is hosted by former biotech editor and broadcaster, the award-winning media veteran Jim Cornall. Base to Base is an Ayr Coastal Media Ltd production.

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