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BioWorld - Wednesday, February 18, 2026
Home » Newsletters » BioWorld

BioWorld

Aug. 4, 2025

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T cells attacking cancer cells

Lepu out-licenses T-cell engagers to newco Excalipoint for $857M

Lepu Biopharma Co. Ltd. has out-licensed two preclinical T-cell engagers to Shanghai-based newco Excalipoint in a deal worth $857.5 million plus equity interest. Under the deal terms, Excalipoint gains an exclusive global license to CTM-012 and CTM-013, developed by Lepu’s Topabody T-cell engager platform. In exchange, Lepu will receive $10 million up front and up to $847.5 million in development and commercial-based milestones, plus tiered royalties on sales. Read More
Blue dollar sign on white background

Workload reductions figure into FDA’s FY2026 user fees

While inflation in the U.S. is hovering below 3%, increases in some FDA user fees for fiscal 2026 are tripling that rate. PDUFA fees for branded prescription drugs and biological products will see a 9% hike come Oct. 1, and the increase in MDUFA fees will more than double the inflation rate with a 7% hike across the board. Read More
Woman holding back in pain

Sham response variability mars Spine’s phase III pain trial

Spine Biopharma Inc. cited an “inconsistent sham control response” among some of the sites in its phase III study testing SB-01 as an intradiscal treatment for patients with chronic low back pain associated with degenerative disc disease. The study, dubbed MODEL, fell short of statistical significance on pain intensity and pain-related function, despite showing numerical and clinically meaningful improvements. Read More

Not much of a wait for the other ACIP shoe drop

The other shoe dropped on the U.S. CDC’s Advisory Committee for Immunization Practices (ACIP) when at least nine liaison organizations were informed by email late July 31 that they would no longer be involved in ACIP’s process of reviewing scientific evidence and informing vaccine recommendations. Read More
Illustration of brain and brain waves, concept of focal seizure

Quitter jitters? Dropouts mar Praxis FOS vormatrigine phase II

Praxis Precision Medicines Inc. is making a change to its upcoming registrational, 400-patient Power2 study – adding a dose arm plus a depression/mood endpoint – based on encouraging phase II data from the Radiant study with vormatrigine in focal onset seizure (FOS) patients over an eight-week period. Specifically, Power2 will test 20 mg, 30 mg, and 40 mg of the drug against placebo for 12 weeks. Read More

NME Digest: Q2 2025

A quarterly dynamic table featuring new molecular entities (NMEs) revealed for the first time in current literature, at congresses and in company communications during the quarter. NMEs include compounds chosen for further pharmacological evaluation or as clinical candidates; new leads whose structural optimization could provide new therapeutic agents; new additions to the structural diversity of known mechanistic classes of drugs; and new pharmacological tools for investigating drug targets. Read More

ICYMI: Week in review, July 28-Aug. 1, 2025

A quick look back at top stories. Read More

Biggest gainers and losers for July 28-Aug. 1, 2025

The top 10 biopharma stock gainers and losers for the week. Read More

Appointments and advancements for Aug. 4, 2025

New hires and promotions in the biopharma industry, including: Biomarin, Certara. Read More

Other news to note for Aug. 4, 2025

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Altasciences, Arrowhead, Biontech, Endo, Mallinckrodt, Moderna, Nosis, Pfizer, Sanofi, Visirna, Voxcell, Yolo. Read More

In the clinic for Aug. 4, 2025

Clinical updates, including trial initiations, enrollment status and data readouts and publications: 4D Molecular, Allogene, Enegenesis, Spine. Read More

Financings for Aug. 4, 2025

Biopharmas raising money in public or private financings, including: Hemostemix, I-Mab, Kazia, Larimar, Medicinova, Oculis, Silexion, Xbrane. Read More

Regulatory actions for Aug. 4, 2025

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Artelo, Lenz, Novartis, Novo Nordisk, Poltreg, Regeneron. Read More

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