UCB and Cradle partner on AI protein design for antibody discovery
UCB will use Cradle's AI-driven protein engineering platform in selected discovery projects, from hit generation to preclinical readiness, with no financial terms disclosed.
Deals, pipeline readouts and company news from across biotech and pharma.
UCB will use Cradle's AI-driven protein engineering platform in selected discovery projects, from hit generation to preclinical readiness, with no financial terms disclosed.
The US life-sciences supplier reported third-quarter revenue of $45.9 million, with TriLink mRNA products up 28%, and raised its full-year revenue and Adjusted EBITDA outlook.
Clinical Diagnostics growth offset a decline in Life Science, while a fair-value change on the Sartorius holding drove GAAP net income of $458.6 million; full-year guidance is unchanged.
The EVO ICL maker reports lower year-on-year net sales for the quarter ended 2 October 2026 and flags label expansions and upcoming presbyopia trials.
The packaging group reported 7% higher quarterly sales of $6.13bn but lowered its adjusted EPS guidance, citing the timing of cost pass-through.
The tobacco leaf and ingredients supplier reported net income of $12.6m, with delayed customer commitments cutting tobacco volumes by about 23%.
The animal health and nutrition company reports an 11% rise in net income to $29.5m, with its guidance still assuming no virginiamycin sales in Brazil.
OPKO Health agreed to sell its remaining BioReference diagnostic operations to Labcorp and reported third-quarter 2026 continuing-operations revenue of $65.4 million.
The US drug distributor also extended its CVS Health partnership to 2032, agreed to buy about 49% of Option Care Health and closed its Precision Medicine Group deal.
The heart-valve maker cites TAVR and TMTT growth, several recent FDA and European approvals, and CMS's final updated TAVR coverage determination.
The company posted a $190.1M third-quarter net loss and says it will file for aficamten in non-obstructive HCM in the US this quarter and in the EU in early 2027.
The bioelectronic medicine company narrowed its quarterly loss to $1.3 million and has asked the FDA to clear Quell for chronic chemotherapy-induced peripheral neuropathy.
The computational drug discovery company reported a $37.7m quarterly net loss and noted FDA Priority Review for Takeda's zasocitinib NDA in plaque psoriasis.
The US biotech posted $45.0m in third-quarter revenue, while FDA approved a label update for its ROS1+ lung cancer drug four months ahead of schedule.
Acadia Pharmaceuticals reported Q3 2026 revenue of $342 million and said DAYBUE (trofinetide) for Rett syndrome has launched in Germany after European Commission approval in August.
The US plasma company reported 31% year-on-year ASCENIV sales growth and kept its full-year revenue guidance, while the FDA responded positively to its pre-IND package for a pneumococcal candidate.
The aesthetics company posted an adjusted EBITDA profit despite a GAAP operating loss, and expects FDA approval of Evolysse Sculpt by the end of the year.
The precision oncology company says Phase 3 breast cancer enrollment should finish in mid-2027, with updated vascular anomaly data due at ASH on 14 December.
Arcutis raised its full-year sales outlook to $535–545 million, and the FDA has set a February 2027 action date for Zoryve cream in infants with atopic dermatitis.
The clinical-stage immune disease biotech says the share consolidation, aimed at regaining Nasdaq bid-price compliance, will cut shares outstanding from about 33.3 million to about 1.11 million.
The company kept its 2026 WAKIX revenue guidance at $1.00B-$1.04B and reported favourable 14-day Phase 1 multiple-ascending-dose data for its orexin-2 agonist BP-205.
Neuronetics narrowed its third-quarter net loss to $1.6M, holding full-year revenue guidance while an FDA 510(k) for an accelerated NeuroStar protocol is under review.
The royalty investor reported third-quarter Portfolio Receipts of $890m, lifted its full-year outlook and bought royalties on two newly commercial dermatology and rare-disease products for $100m each.
The US maker of the NeuroStar TMS system cites revenue and patient figures in an investor presentation that also flags going-concern and credit facility risks.
The preclinical contract research group reported Q3 revenue of $982.7 million, down 2.2% as reported after divestitures, and raised its full-year revenue and non-GAAP earnings outlook.
The wholesaler's full-year sales rose 5.0%, helped by the OneOncology acquisition, while it guides fiscal 2027 adjusted diluted EPS to $19.40-$19.75.
The US healthcare group lifted full-year profit and cash-flow forecasts, citing stronger performance in its insurance and pharmacy divisions, and flagged expanded GLP-1 weight management offerings.
The orthopaedic device maker reported hip and technology-segment growth, a drop in knees, and raised its 2026 organic growth and adjusted earnings guidance.
The US medical supplies group reported third-quarter net income of $318 million, helped by tariff refunds, and lifted its full-year organic sales growth guidance while holding its EBITDA outlook.
Geron reported a 5% quarterly rise in Rytelo sales and a small profit, lowered its 2026 operating expense guidance and discontinued its Phase 3 IMpactMF myelofibrosis trial.
Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.