| 01 | From the Editor |
| 02 | The Big Picture — AMR: We Have a Pipeline, But Is It Enough? |
| 03 | Drug & Therapeutics Watch — New Medicines Worth Knowing |
| 04 | Clinical Trial Radar |
| 05 | Funding Radar — Opportunities Open Now |
| 06 | Africa Opportunity Desk |
| 07 | ECR, Scholar & Postdoc Opportunity Board |
| 08 | Conference Radar |
| 09 | Molecule of the Issue — Daraxonrasib |
| 10 | From Bench to Bedside |
| 11 | Tools Every Health Researcher Should Know |
| 12 | AeternuVita Corner |
Plus: Opportunity of the Month, and a note from the editor on what's next.
Medicine is entering one of its most consequential periods. Artificial intelligence is changing how therapeutic targets are identified. New chemical and biological modalities are challenging diseases once considered difficult or impossible to treat. Precision medicine is becoming increasingly practical. Clinical trials are testing new approaches to cancer, infectious diseases, neurological disorders and rare diseases. At the same time, antimicrobial resistance continues to threaten some of the foundations on which modern medicine depends.
Yet another challenge exists: information is fragmented. A researcher may need one platform to discover funding, another to follow clinical trials, another to track newly approved medicines, and several more to identify conferences, fellowships, training programmes and potential collaborators.
Whether you are a student taking your first steps into research, an early-career researcher establishing independence, a clinician, an established investigator, or simply someone interested in how science is transforming health, we want AeternuVita Insights to become one of the places you look first.
Welcome to our maiden issue.
From Editor's Desk
Scientific discovery is accelerating, but access to useful scientific information remains remarkably uneven. Every week, funding calls open and close. New medicines receive regulatory approval. Clinical trials report results. Researchers publish potentially transformative discoveries. Conferences create opportunities for collaboration. Fellowships capable of changing scientific careers appear across different continents.
The challenge is increasingly not the absence of information. It is finding the right information at the right time — and understanding why it matters.
AeternuVita Insights begins with that challenge. Our vision is to create a trusted meeting point between discovery, medicine and opportunity. We will follow important developments from molecules at the laboratory bench through preclinical development, clinical trials and ultimately patient care. Alongside the science, we will identify funding, fellowships, conferences, training and collaborative opportunities that can help researchers move their ideas and careers forward.
Particular attention will be given to opportunities accessible to researchers in Africa and other low- and middle-income settings, without losing our global perspective. This publication will evolve with its community. But its guiding philosophy will remain unchanged: science should ultimately improve life.
Antimicrobial resistance is not simply a microbiology problem. It threatens surgery, cancer chemotherapy, transplantation, neonatal care, and virtually every area of medicine that depends on reliable control of bacterial infection.
WHO's antibacterial pipeline analysis provides an uncomfortable picture: of the antibacterial products in clinical development, only a minority target WHO bacterial priority pathogens, and fewer still satisfy WHO's own criteria for genuine innovation. The preclinical landscape is larger — but the large majority of that early-stage work is concentrated in high-income countries.
The problem therefore extends beyond discovering another antibacterial molecule. The field needs genuinely differentiated mechanisms, activity against priority resistant pathogens, successful translation through clinical development, sustainable commercial models, and equitable access to resulting medicines.
New mechanisms of action — compounds capable of attacking bacterial vulnerabilities not exploited by existing antibiotic classes.
Resistance-breaking combinations — strategies that restore activity to existing drugs or inhibit resistance mechanisms.
Pathogen-specific therapeutics — precision approaches that may reduce unnecessary microbiome disruption.
Non-traditional antibacterials — phages, antibodies, peptides, antivirulence agents, and microbiome-based interventions.
Translation, not activity alone — a compound with an excellent MIC is the beginning of a drug-development story, not its conclusion.
The next breakthrough in AMR may not simply be a stronger antibiotic. It may emerge from a completely different way of thinking about how pathogens can be selectively targeted, disarmed, or made vulnerable.
The US FDA had listed 36 novel drug approvals for 2026 by 28 August. Among the most recent are several scientifically interesting examples.
Its approval is especially notable because oncogenic RAS biology has historically represented one of drug discovery's most difficult target spaces. In the pivotal RASolute 302 trial, median overall survival was 13.2 months with daraxonrasib versus 6.7 months with standard chemotherapy.
A first-in-class hepcidin mimetic — the first approved PV therapy to work by directly regulating iron availability rather than suppressing red blood cell production downstream.
Adds another important therapeutic development for immune-mediated disease.
Used in combination therapy for previously treated patients.
A particularly interesting development in mechanism-based treatment of sleep disorders.
Also worth watching: in June 2026, the FDA approved tebipenem pivoxil (Utebzi) — described by the agency as the first oral carbapenem therapy for complicated urinary tract infections, an important development from an antimicrobial-drug perspective.
One purpose of this section will be to follow medicines before they reach pharmacies.
A major recent example comes from lung cancer. A late-stage study of osimertinib plus savolitinib in previously untreated EGFR-mutated advanced non-small-cell lung cancer with MET overexpression reported improved progression-free survival compared with osimertinib alone.
The broader lesson extends beyond this particular combination: combination precision therapy is becoming increasingly important. Tumours evolve. Signalling networks compensate. Resistance emerges. Future oncology will increasingly require researchers to understand not only which molecular target drives a cancer, but also which escape pathways become important when that target is inhibited.
Phase I — Is the intervention sufficiently safe, and what dose should advance?
Phase II — Is there an early signal of therapeutic activity?
Phase III — Does the intervention outperform or add meaningful value to current care?
Regulatory milestone — Has the evidence become strong enough to change treatment?
Supports bold and creative research capable of generating major shifts in understanding related to human life, health and wellbeing.
A major opportunity for researchers transitioning toward research independence.
For researchers developing their independent research identity and programme.
Supports academic researchers translating laboratory discoveries into novel adult-cancer therapeutics using antibody or small-molecule approaches. Researchers at universities and research institutes worldwide may apply, subject to scheme requirements.
Includes opportunities for international researchers, including postdoctoral and established research pathways.
Supports development and validation of clinical outcomes and biomarkers relevant to ALS clinical trials.
Focused on integrating imaging and multimodal data with AI for precision medicine, including academic–industrial partnerships. Foreign organizations and/or foreign components may be eligible depending on the specific call.
Supports early-career researchers (2–7 years post-PhD) to establish an independent research team in the EU or an associated country. Up to €1.5 million over 5 years. Open since 22 July 2026.
UK Medical Research Council curiosity-driven research funding reopened in April 2026 under a reformed process. Applications are assessed on a rolling basis, with funding decisions made twice yearly, in June and December.
The Gates Foundation runs Grand Challenges as a continuously rotating set of open requests for proposals across global health priorities, including a recurring track on innovations for eliminating neglected tropical diseases. Individual RFPs open and close throughout the year with their own deadlines.
A $15 million NIAID cooperative agreement to design, implement, and manage clinical research addressing key clinical questions in bacterial and fungal AMR. Foreign components may be eligible.
NIAID cooperative agreement (UM1, clinical trial required) supporting a clinical trials network for infectious disease. Foreign components may apply.
The world's largest prize for mental health science. Overall winner receives US$1 million; three finalists receive US$250,000 each. Open to research teams and small/medium organisations worldwide championing new interventions for anxiety, depression, or psychosis.
Supports research on how evidence-based health interventions are adopted and scaled in real-world settings. Two mechanisms available (R03 and R21); foreign organisations and components may apply.
The Africa Research Excellence Fund and UKRI Medical Research Council programme is designed to strengthen the capacity of emerging African researchers to compete for major global-health funding. The programme targets researchers who are citizens of African countries, employed by recognised African universities or research institutions, and at the early stages of leading research teams.
The 2026 programme demonstrates the scale of Africa–Europe investment now entering infectious-disease and health-system research. Its competitive calls include programmes addressing TB drug development, lower respiratory tract infections, HIV co-infections and co-morbidities, climate and health, ethics/regulation/pharmacovigilance, and digital innovation and AI in African healthcare. For researchers building African clinical and translational collaborations, EDCTP should remain permanently on the funding radar.
A research capacity-building initiative supporting PhD, postdoctoral, and early-career researchers working on leishmaniasis (a neglected tropical disease) across Africa. Supports development of independent research leaders in epidemiology, diagnostics, and treatment strategy for this disease area.
Development of affordable multiplex assays for micronutrient status, infection, and inflammation. LMIC participation is encouraged.
Basic or translational research; international applicants eligible.
Support for independently organised scientific meetings and training events; international eligibility applies subject to membership requirements.
For eligible early-career researchers in neurological research.
Supports development and validation of biomarkers with clinical relevance to Alzheimer's disease and related dementias.
Career and scientific mentorship in clinical microbiology and infectious diseases, with pathways relevant to scientists in low- and lower-middle-income countries.
The Drug Discovery and Development Centre at the University of Cape Town — Africa's first fully integrated drug discovery centre — runs recurring postdoctoral fellowships in medicinal chemistry across malaria, TB, and AMR research. The most recent round closed 28 February 2026; new rounds are posted periodically, so this is worth checking regularly rather than a one-time deadline.
Theme: "From Crisis to Resilience: Innovating for Health." More than 4,000 on-site participants, 400+ speakers, and 75+ sessions expected across global health, health systems, innovation, security, and policy.
One of the particularly relevant meetings for drug-discovery scientists, spanning emerging targets, molecular biology, preclinical discovery, and early clinical development. Regular registration deadline: 30 September 2026.
Theme: "Innovating Together for Resilient Global Health." A flagship event for infectious-disease research and Africa–Europe global-health collaboration.
Annual summit connecting global cancer-care researchers, clinicians, and institutions to advance oncology capacity-building worldwide.
Hosted by the U.S. National Cancer Institute. Free virtual access makes this one of the more accessible major cancer-research conferences for researchers without international travel funding.
When a Historically Difficult Target Becomes Drugable
RAS mutations are among the most important oncogenic alterations in human cancer, but the structural and biochemical properties of RAS proteins historically made direct pharmacological inhibition exceptionally challenging.
That landscape is changing. The August 2026 FDA approval of daraxonrasib for metastatic pancreatic adenocarcinoma provides an excellent case study in an important principle of modern drug discovery:
Advances in structural biology, medicinal chemistry, molecular pharmacology, and precision oncology can progressively transform difficult biological targets into therapeutic opportunities. That principle extends far beyond cancer.
Researchers understandably celebrate when a newly synthesized compound produces impressive biological activity. But the distance between an active compound and an approved medicine is enormous.
And even then the story continues through pharmacovigilance, implementation, access, and real-world evidence.
Biological activity is evidence of potential. Translation determines whether that potential becomes medicine.
One of the most important resources for tracking registered clinical studies, interventions, sponsors, recruitment status, and study outcomes.
A valuable resource for understanding global health research activity, including therapeutic pipelines and R&D gaps.
Still foundational for biomedical literature discovery.
Useful for searching clinical-trial registration information across participating registries internationally.
Future issues will introduce specialist resources for drug discovery, structural biology, computational chemistry, genomics, funding intelligence, and scientific writing.
AeternuVita is being built around a simple conviction: science should not end with discovery — it should reach humanity.
Our scientific interests sit at the intersection of chemistry, biology, and medicine, with a long-term focus on therapeutic discovery and translation for some of humanity's most difficult health challenges.
But AeternuVita is also about people. We believe scientific impact requires researchers to have access not only to laboratories, but also to knowledge, mentorship, collaboration, and opportunity. AeternuVita Insights is one step toward building that ecosystem — starting from an active research programme today, growing deliberately from there.
For ambitious researchers asking fundamental questions capable of changing our understanding of human health and life.
Don't simply ask: Am I eligible?
Also ask: Is my research question important enough? Is my hypothesis compelling? And have I explained why solving this problem changes the field?
Tell AeternuVita Insights — we want this publication to grow into a community-powered resource for science and health.