Drug Discovery & Development
VerifiedOnline/Digital
Drug Discovery and Development covers strategies and technologies related to pharmaceutical research and development and drug formulation. We report on innovative drug introductions and promising pipeline candidates from Big Pharma and smaller players, as well as relevant clinical trial trends. WIth the growing interest in artificial intelligence and machine learning in drug discovery and development, we provide insights into the latest AI-driven methodologies, platforms, and tools being harnessed by the industry, showcasing real-world applications and case studies that highlight the tangible benefits and challenges of integrating these technologies. Source
Actions
Media Outlet details
| Scope | International, Trade/B2B |
|---|---|
| Language | English |
| Country | United States of America |
|
Similarweb UVM |
Request pricing |
|
Comscore UVM |
Request pricing |
| Accepts contributed content | Yes |
Recent Articles
Search ArticlesLilly offers up to $3.8 billion for AtaiBeckley in bet on ‘God molecule’ found in toad venom
The Sonoran Desert toad (Incilius alvarius, formerly Bufo alvarius), whose parotoid gland secretions contain high concentrations of 5-MeO-DMT. Image via Wikipedia. Eli Lilly has agreed to acquire AtaiBeckley for $2.8 billion upfront, plus up to $1 billion in contingent value rights, in a deal that could reach $3.8 billion.
Drug Discovery & Development parent company WTWH Media is now Arrowfly
WTWH Media, the parent company of Drug Discovery & Development, announced on July 13 that it has renamed itself Arrowfly. The change applies to the corporate entity. DDD keeps its name, its URL, its newsletter, its editorial staff and its archives. The Cleveland-based company operates more than 40 B2B media brands and more than 45 industry events across three networks, spanning engineering; healthcare and life sciences; and food, retail and hospitality.
CEO of CDMO AustinPx on its exclusive agreement with Thermo Fisher’s Patheon division
A researcher at work in an AustinPx laboratory. (Image courtesy of AustinPx) Thermo Fisher’s Patheon division has signed an exclusive agreement with AustinPx to install the Texas CDMO’s KinetiSol technology at Patheon’s Bend, Oregon, and Cincinnati sites. AustinPx specializes in bioavailability enhancement for orally delivered small molecules, and the placement plugs into Patheon’s Quadrant 2 platform, which applies AI/ML to formulation prediction.
How ConcertAI turned CancerLinQ into a point-of-care oncology intelligence platform
More than a decade ago, the American Society of Clinical Oncology (ASCO) launched CancerLinQ, a platform designed to pool electronic health record data from oncology practices, turning routine patient encounters into a learning system. The platform has since become central to ConcertAI, an oncology-focused AI and real-world data company, which acquired it from ASCO in December 2023. Before the acquisition, CancerLinQ’s most widely used function was automated reporting.
Moderna bets on mRNA’s second act with cancer, autoimmune programs and AI research platform
An overview showing Moderna’s diverse technological focuses map [Image courtesy: Moderna] At its recent annual Science Day, Moderna signalled a strategic expansion beyond its established vaccine and rare disease franchises, unveiling new programs in in vivo CAR-T and solid tumor oncology. The firm also revealed an AI-driven research platform it says will accelerate the pace of drug discovery across its pipeline.
PharmSci 360 2026 heads to New Orleans this October
The American Association of Pharmaceutical Scientists (AAPS) will hold its 2026 PharmSci 360 meeting October 25 to 28 at the Ernest N. Morial Convention Center in New Orleans. The event is the association’s flagship annual gathering, drawing thousands of scientists from across academia, industry, and government. AAPS, which counts roughly 7,000 members, positions PharmSci 360 as a meeting that pairs the scale of a large scientific conference with the focus of a smaller specialist forum.
A GLP-1 bone study shows why matching matters in real-world evidence
A clinician sees a pattern in their own patients. They run the numbers to check it, and the numbers seem to confirm what they already suspected. But that confirmation might not be real. “Often a clinician at the point of care will come to us with a hunch — ‘I’ve seen a bunch of these patients, I think this might be going on’ — and when you run the unmatched analysis, without statistical balancing, it can appear to confirm that hunch.
Calderasib’s real innovation: designed for combination, not raw potency
Merck didn’t design calderasib to be the most potent KRAS G12C inhibitor on its own. It was designed to be the most combinable inhibitor. The KRAS gene encodes a protein that signals for cell growth. It cycles between active and inactive states, signaling when cells should divide. Although it is one of the most commonly mutated genes across human cancers, it was considered undruggable for decades due to its smooth surface.
Insuring the trip: an underwriter on what it will take for approved psilocybin can become a real business
More than five decades after the Controlled Substances Act that President Richard Nixon signed in 1970 placed psilocybin in Schedule I, the same tier as heroin and reserved for drugs the federal government deemed to have no accepted medical use, the compound is on the verge of becoming the first classic psychedelic to win FDA approval. Formal approval may not arrive within the 12-month window Secretary Robert F.
How most-favored-nation pricing is reshaping generic drug economics, according to Dr. Reddy’s finance director
In the U.S. market, generics play a significant role in reducing overall drug spending. The FDA, for instance, estimated that the generics it approved in 2022 alone saved $18.9 billion in their first year on the market. Those savings come out of margins that keep thinning, because generic retail prices are in sustained deflation, as Brookings documented in March 2026 testimony to the Senate Aging Committee.