Lilly’s new obesity pill linked to ‘serious’ safety signals, FDA requests more data

BioSpace

The FDA is asking Eli Lilly to submit cardiovascular and liver safety data from an ongoing Phase 3 trial of Foundayo by July.

RegulatoryRead full story

Takeda continues to prune partnerships, cuts ties with mRNA-targeting Veritas In Silico

BioSpace

After divorcing Denali Therapeutics earlier this month, Takeda is now splitting up with Veritas In Silico, pulling back from a partnership that advanced novel small-molecule drugs targeting mRNA.

M&A / DealsRead full story

Parkinson’s charity partners Biognosys on biomarker project

Pharmaphorum

A new R D project will try to develop assays for LRRK2, a biomarker linked to Parkinson’s that has emerged as a major drug target in the disease.

M&A / DealsRead full story

Daiichi exits OTC, with $1.55bn unit sale to Suntory

Pharmaphorum

Daiichi Sankyo has agreed to sell its consumer health unit to food and beverage giant Suntory, following a well-trodden path for big pharma companies.

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BMS makes a Beeline, bringing 5 assets to biotech’s $300M precision immunology debut

BioSpace

Leading Beeline Medicines’ pipeline is afimetoran, which is in Phase 2 development for systemic lupus erythematosus with data expected later this year.

M&A / DealsRead full story

Whitepaper: CDMOs at a Crossroads

BioSpace

In this whitepaper, BioSpace reviews the major trends impacting the CDMO sector and the evolving relationship between sponsors and providers.

ManufacturingRead full story

Scientists issue call to arms over antifungal resistance

Pharmaphorum

Infectious disease experts from around the world are calling for concerted action to combat a “silent surge” in resistance to antifungal drugs.

Policy / PricingRead full story

Amazon launches AI drug discovery platform

Pharmaceutical Technology

Amazon has already collaborated with Memorial Sloan Kettering Cancer Center with its AI drug discovery software.

OtherRead full story

J&J leans on Tremfya, cancer drugs to overcome Stelara losses

BioPharma Dive

A growing multiple myeloma franchise helped the pharmaceutical giant top Wall Street s expectations and surpass $15 billion in first-quarter drug sales.

CommercialRead full story

With nearly a quarter billion in Q1, J&J targets $100B revenue in 2026

BioSpace

With robust sales performance from oncology darling Darzalex and immunology superstar Tremfya, Johnson & Johnson is “off to a fast start in 2026,” CEO Joaquin Duato told investors on Tuesday.

CommercialRead full story

Lilly boosts ADC portfolio with CrossBridge Bio deal

BioPharma Dive

Worth up to $300 million, the buyout is Lilly s latest of an ADC maker and adds technology for making dual-payload therapies.

M&A / DealsRead full story

Lilly investing billions to prepare for overseas oral GLP-1 launches

BioSpace

With many overseas patients preferring orals to injectables, Eli Lilly has filed for approval of orforglipron in more than 40 countries and is building manufacturing capacity to support the obesity dr

ManufacturingRead full story

FDA renews criticism of trial sponsors over transparency

Pharmaphorum

The FDA has launched a drive to get clinical trial sponsors to disclose the results of studies – even if they are negative.

RegulatoryRead full story

Mapping the Vertical Integration of Insurers, PBMs, GPOs, Specialty Pharmacies, and Healthcare Services: DCI’s 2026 Update

Drug Channels

It’s time for Drug Channels Institute’s (DCI) annual update of vertical integration among insurers, PBMs, specialty pharmacies, and healthcare services within U.S.

Market AccessRead full story

Novo Nordisk partners OpenAI on R&D “transformation”

Pharmaphorum

Seeking an R D edge, Novo Nordisk has become the latest big pharma group to forge an alliance with tech giant OpenAI.

M&A / DealsRead full story

Travere Therapeutics gains FDA approval for sparsentan in FSGS

Pharmaceutical Business Review

The approval makes Filspari the first and only FDA-approved medicine to treat FSGS, expanding its use beyond IgA nephropathy (IgAN) into a second rare kidney condition.

RegulatoryRead full story

Travere Therapeutics gains FDA approval for sparsentan in FSGS

Pharmaceutical Technology

Travere Therapeutics has received FDA approval for Filspari to reduce proteinuria in patients aged eight years and over with FSGS without nephrotic syndrome.

RegulatoryRead full story

MSD, Daiichi Sankyo’s ifinatamab deruxtecan receives FDA priority

Pharmaceutical Business Review

The treatment targets adult patients with ES-SCLC who have experienced disease progression on or after platinum-based chemotherapy.

RegulatoryRead full story