Drug Discovery and Development
HanchorBio announces US FDA clearance of IND application for HCB303, a next-generation trispecific immunotherapy
Lundbeck presents phase 1b data for Lu AF28996 in advanced Parkinson’s disease, as phase 2 trial begins
Beactica Therapeutics selects BEA-28 as a preclinical candidate and first-in-class TEAD degrader for biomarker-selected cancers
Carbogen Amcis announces successful first FDA pre-approval inspection at its Vionnaz site
Thermo Fisher Scientific showcases new solutions and expanded capabilities to accelerate drug development at CPHI Milan 2026
Novai publishes study supporting use of DARC imaging technology to identify patients at risk of central vision loss from macular atrophy
nPhase.AI becomes the industry’s first AI-native enterprise platform for end-to-end clinical data management
Yourgene Health Insight DPYD assay achieves IVDR accreditation
Takeda Receives US FDA approval of Mimrylo (rusfertide), marking a potential shift in the treatment paradigm for polycythaemia vera
uniQure announces submission of biologics license application for ifezuntirgene inilparvovec (AMT-130) in Huntington’s Disease
FDA approves Imaavy (nipocalimab-aahu) as first-ever treatment for warm autoimmune haemolytic anaemia (wAIHA), representing a landmark advancement for patients
GSK to advance mRNA seasonal flu vaccine candidate to phase 3 following positive phase 2 data
FDA approves Gilead’s Bixlenvo, a new once-daily single tablet option for virologically suppressed adults with HIV, including those on complex regimens
European Commission approves Jascayd, bringing well-tolerated, novel oral treatment for IPF and PPF to the EU
AstraZeneca completes global license agreement for oral EGFR inhibitor Zegfrovy for lung cancer
Enhertu plus pertuzumab approved in the EU as first new regimen in more than a decade for the 1st-line treatment of patients with HER2-positive...
Abbott receives FDA authorisation for world’s first dual glucose-ketone sensing technology for people with diabetes
Kali Therapeutics Receives US FDA Clearance for KT501 Investigational New Drug Application
Lubrizol targets drug delivery challenges at CPHI Milan
FairJourney Bio delivers antibody engineering for novel tumour-conditional IL-12 therapeutic approach that unlocks the potential of localised cytokine activation
Clinical Trials Insights
Anixa Biosciences announces first case of stable disease for three months in ovarian cancer CAR-T clinical trial
Vial doses first patient with asthma in phase 1b study of Vial’s IL-13 x TSLP, a bispecific antibody designed for twice-yearly dosing
Lundbeck presents phase 1b data for Lu AF28996 in advanced Parkinson’s disease, as phase 2 trial begins
AbbVie and Genmab announce epcoritamab in combination with R-CHOP demonstrates significant improvement in progression-free survival versus R-CHOP in patients with newly diagnosed diffuse large...
New partnership expands UK trial access for potential world-first vaccine against killer infection
VIDEOS
Pharma in Healthcare
Abbott receives FDA approval for new CardioMEMS HF system capabilities that help patients engage in the care of their heart condition
American Regent issues voluntary nationwide recall of three lots of epinephrine injection, due to the presence of particulate matter and lack of assurance of...
Roche expands cyclospora testing portfolio to support US public health response
Sanofi’s MenQuadfi approved in the EU for use in infants from age six weeks against invasive meningococcal disease
Nipro Corporation receives FDA 510(k) clearance for Elisio-HX, introducing HDs to the United States
Technology and Automation
Abbott receives FDA approval for new CardioMEMS HF system capabilities that help patients engage in the care of their heart condition
Hovione to commission world’s first ConsiGma CDC flex, bringing next-generation continuous tableting to the US
Brainomix and Endeavor present positive results from quantitative image analysis of phase2a idiopathic pulmonary fibrosis (IPF) trial
Bio-Rad launches PTC Harmony 96 and PTC Harmony Deepwell thermal cyclers
PCI Pharma Services announces US$1 billion expansion of US sterile fill-finish and drug-device delivery combination capabilities
Drug delivery and supply chain
Dr Oregonin completes US FDA registration for Oltis Dental-X, unveiling oral-care innovation rooted in trans-Pacific alder research
Esteve CDMO expands US capacity with additional $17.5 million investment in Morton Grove
Hovione to commission world’s first ConsiGma CDC flex, bringing next-generation continuous tableting to the US
West to highlight industry leadership in packaging and containment at CPHI worldwide
Yourgene Health Insight DPYD assay achieves IVDR accreditation
Conferences and events
Thermo Fisher Scientific showcases new solutions and expanded capabilities to accelerate drug development at CPHI Milan 2026
CPHI Milan 2026: The Must-Attend Event for Pharma Professionals
World Health Expo (WHX) in Dubai 2027
2026 PharmSci 360 launches two innovator-curated tracks, developed by leading scientific experts
LSX Investival Showcase London
Finance, mergers and appointments
Consano Bio raises more than US $15 million in oversubscribed financing to advance C-1101 in chronic painful lumbosacral radiculopathy (chronic sciatica)
CellCarta establishes strategic partnership with Waters to advance companion diagnostics development
Ontario contributes $1.7 million investment to advance life sciences innovation at Piramal Pharma’s Aurora facility
Evotec announces Chief Scientific Officer transition
Alcami strengthens commercial operations with appointment of Will Isom as Vice President of laboratory services sales
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Thryv Therapeutics has entered into an exclusive, worldwide, royalty-bearing patent and know-how license agreement with the Spanish National Research Council (Consejo Superior de Investigaciones Científicas, the Autonomous University of Madrid (Universidad Autónoma de Madrid) and Fundación de la Universidad Autónoma de Madrid).
The agreement became effective on 1 July 2026.
Thryv holds rights across all fields of use and in all territories, with the right to sublicense.
Thryv’s existing clinical SGK1 inhibitor candidates were built through independent medicinal chemistry on a single in-licensed scaffold, supported by a library of more than 500 synthesised analogues and a granted selection patent estate.
The CSIC/UAM series is a distinct chemotype arising from an entirely separate discovery programme, a genuinely new starting point rather than an extension of the existing series. Adding a second independent series gives Thryv the ability to match chemistry to indication, continuing to optimize its current molecules for cardiac and cardiometabolic diseases while developing compounds designed from the outset to reach the brain.
The licenced invention was developed by research groups with complementary expertise directly relevant to that ambition: the medicinal chemistry group led by Dr Ana Martínez and Dr Carmen Gil and the cardiovascular group led by Dr Eduardo Oliver Pérez at CSIC’s Centro de Investigaciones Biológicas Margarita Salas, together with the neurobiology group led by Dr Isabel Lastres-Becker at UAM’s Institute for Biomedical Research and the vascular pharmacology group led by Dr Ana Briones Alonso at UAM’s Department of Pharmacology.
Activated SGK1 sits at the intersection of several pathways central to neurodegeneration. Published work has implicated the kinase in tau phosphorylation, in the handling of misfolded and aggregating proteins, in neuroinflammatory signalling, and in FOXO- and NRF2-dependent cellular stress responses. This disease biology is directly relevant to Parkinson’s disease, Alzheimer’s disease and related tauopathies.


