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Clinical Trials
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Agenus to Highlight Emerging Survival Plateaus with Botensilimab/Balstilimab in Oral Presentation of Study in Refractory Patients Across Five Tumor Types at ESMO 2025

LEXINGTON, Mass.--(BUSINESS WIRE)--Agenus Inc. (Nasdaq: AGEN), a leader in immuno-oncology, today announced that four abstracts highlighting clinical progress across its botensilimab and balstilimab immunotherapy programs have been accepted for presentation at the European Society for Medical Oncology (ESMO) Congress 2025, taking place in Berlin, Germany from October 17-21. The highlight is an oral presentation that will feature emerging survival plateaus from a study of botensilimab plus balst...
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Bayer Provides Regulatory Update on Elinzanetant for the Treatment of Moderate to Severe Hot Flashes Due to Menopause

WHIPPANY, N.J.--(BUSINESS WIRE)--Bayer Provides Regulatory Update on Elinzanetant for the Treatment of Moderate to Severe Hot Flashes Due to Menopause...
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Leveragen and Propeller Bio Announce Strategic Collaboration to Advance Antibody and Protein Therapeutics

BOSTON & SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Leveragen, a Boston-based biotechnology company pioneering next-generation in vivo antibody discovery platforms, announced today a strategic collaboration with Propeller Bio, a newly launched biotechnology company focused on antibody and protein-based therapeutics. As part of the partnership, Propeller Bio will support the continued development of Leveragen’s antibody discovery platforms through a strategic investment. In turn, Propeller wi...
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Venova Technologies Awarded $2.23M SBIR Phase II Grant From NIH For Novel Contraceptive Device

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Venova Technologies, Inc., a women-led startup developing a novel long-acting, hormone-free and copper-free female birth control device, has been awarded a $2.23M Small Business Innovation Research (SBIR) Phase II Grant from the National Institutes of Health (NIH). The SBIR program is a highly competitive, awards-based program designed to stimulate technological innovations developed by U.S. small businesses on a path to commercialization. This Phase II award...
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KalVista Pharmaceuticals Receives Positive CHMP Opinion for Sebetralstat for the Treatment of Hereditary Angioedema Attacks

CAMBRIDGE, Mass. & SALISBURY, England--(BUSINESS WIRE)--KalVista Pharmaceuticals, Inc. (Nasdaq: KALV) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending marketing authorization for sebetralstat, a novel oral plasma kallikrein inhibitor, for symptomatic treatment of acute attacks of hereditary angioedema (HAE) in adults and adolescents aged 12 years and older. The European Commission (E...
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TRYNGOLZA® (olezarsen) recommended for approval in the EU by CHMP for familial chylomicronemia syndrome (FCS)

CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) and Sobi® today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has adopted a positive opinion of TRYNGOLZA® (olezarsen) as an adjunct to diet in adult patients for the treatment of genetically confirmed familial chylomicronemia syndrome (FCS). The positive opinion is now referred to the European Commission (EC) for an approval decision, which is expected by Q4...
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Riassunto: Incyte presenterà i dati iniziali per il suo anticorpo bispecifico diretto contro TGFβR2×PD-1 (INCA33890) e il suo inibitore selettivo della mutazione KRAS G12D (INCB161734) al Congresso 2025 della European Society of Medical Oncology (ESMO)

WILMINGTON, Del.--(BUSINESS WIRE)--Incyte (Nasdaq:INCY) oggi ha annunciato che la Società presenterà i dati principali del suo portafoglio di farmaci oncologici al prossimo Congresso 2025 della European Society of Medical Oncology (ESMO), che si terrà a Berlino dal 17 al 21 ottobre prossimo. Il testo originale del presente annuncio, redatto nella lingua di partenza, è la versione ufficiale che fa fede. Le traduzioni sono offerte unicamente per comodità del lettore e devono rinviare al testo in...
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ImmunityBio Reports 60% Increase in Revenue in Q2 2025, with Year-to-Date Sales of $43 Million and 246% Unit Growth Since J-Code with Regulatory Updates

CULVER CITY, Calif.--(BUSINESS WIRE)--ImmunityBio, Inc. (NASDAQ: IBRX), a leading immunotherapy company, today announced preliminary financial results for the fiscal quarter ended June 30, 2025, and clinical progress across its pipeline. Key Highlights Q2 2025 Revenue Growth with Continued Strong Sales Momentum: $26.4 million, up 60% from Q1 2025, with year-to-date sales of ~$43 million. ANKTIVA® Unit Growth Since J-Code: 246% unit sales volume growth in 1H 2025 compared to 2H 2024. Cash Positi...
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Incyte présentera les premières données relatives à son anticorps bispécifique ciblant TGFβR2×PD-1 (INCA33890) et à son inhibiteur sélectif de KRAS muté en G12D (INCB161734) lors du congrès 2025 de la Société européenne d’oncologie médicale (ESMO)

WILMINGTON, Delaware.--(BUSINESS WIRE)--Incyte (Nasdaq : INCY) a annoncé aujourd’hui que la société présentera les données clés de son portefeuille de produits oncologiques lors du prochain congrès de la Société européenne d’oncologie médicale (ESMO) 2025, qui se tiendra du 17 au 21 octobre à Berlin. « Nous sommes impatients de présenter les dernières découvertes de notre portefeuille de produits oncologiques lors du congrès de cette année, notamment les premières données sur notre anticorps bi...
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Samenvatting: Incyte presenteert eerste gegevens over zijn TGFβR2×PD-1-gerichte bispecifieke antilichaam (INCA33890) en zijn selectieve G12D-gemuteerde KRAS (INCB161734)-remmer tijdens het congres van de European Society of Medical Oncology (ESMO) in 2025

WILMINGTON, Del.--(BUSINESS WIRE)--Incyte (Nasdaq:INCY) kondigde vandaag aan dat het bedrijf belangrijke gegevens van zijn oncologieportfolio zal presenteren op het komende European Society of Medical Oncology (ESMO) Congres 2025, dat van 17-21 oktober in Berlijn wordt gehouden. Deze bekendmaking is officieel geldend in de originele brontaal. Vertalingen zijn slechts als leeshulp bedoeld en moeten worden vergeleken met de tekst in de brontaal, die als enige rechtsgeldig is....