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CELH Deadline: Rosen Law Firm Urges Celsius Holdings, Inc. (NASDAQ: CELH) Stockholders to Contact the Firm for Information About Their Rights

NEW YORK--(BUSINESS WIRE)--Rosen Law Firm, a global investor rights law firm, reminds investors about a class action on behalf of purchasers of securities of Celsius Holdings, Inc. (NASDAQ: CELH) between February 21, 2025 and June 3, 2026. Celsius describes itself as a company that “develops, processes, manufactures, markets, sells, and distributes products including energy drinks.”For more information, submit a form, email attorney Phillip Kim, or give us a call at 866-767-3653.The Allegations:...
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BeOne Medicines在ESMO 2026上公布針對難治性肝癌和肺癌的具說服力數據

加州聖卡洛斯--(BUSINESS WIRE)--(美國商業資訊)-- 全球性腫瘤公司BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235)今日在10月23日至27日於馬德里舉行的2026年歐洲腫瘤內科學會(ESMO)大會上,公布了其重點實質腫瘤疾病領域多款差異化試驗中藥物的最新數據。報告涵蓋胃腸道腫瘤、肺癌和乳癌,體現了BeOne實質腫瘤業務不斷強化的發展動力。 BeOne實質腫瘤醫療長Mark Lanasa, M.D.博士表示: 「在本次ESMO大會上,我們展示了將合適的治療方式與疾病生物學特徵相匹配的策略如何轉化為有意義的臨床進展。我們的GPC3 x 4-1BB雙特異性抗體在重度經治肝細胞癌(HCC)病患中繼續表現出良好的耐受性,並在更長隨訪期下展現出持久活性;同時,具有腦滲透能力的PRMT5抑制劑和標靶作用於CEA之ADC的首次臨床數據,進一步擴大了我們在非小細胞肺癌領域的創新布局。結合我們在乳癌領域展開的CDK4抑制劑全球第三期KANDELA-302研究,這些進展代表BeOne實質腫瘤研發產品線正從有前景的科學...
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Ivonescimab Plus Chemotherapy Demonstrates Overall Survival Superiority Compared to Durvalumab Plus Chemotherapy in First-Line Treatment of Patients with Advanced Biliary Tract Cancer in HARMONi-GI1 Study Conducted by Akeso in China

MIAMI--(BUSINESS WIRE)--Summit Therapeutics Inc. (Nasdaq: SMMT) today noted that its partner Akeso Inc. announced positive results from the Phase III HARMONi-GI1 study evaluating the novel, potential first-in-class investigational bispecific antibody ivonescimab plus chemotherapy compared with durvalumab plus chemotherapy as a first-line treatment for patients with advanced biliary tract cancer (BTC). These data are featured in today’s Presidential Symposium II at the European Society for Medic...
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Sonesitatug vedotin reduced the risk of death by 42% in 2nd and later-line CLDN18.2-positive advanced gastric/GEJ cancers in CLARITY-Gastric01

WILMINGTON, Del.--(BUSINESS WIRE)--Positive results from the CLARITY-Gastric01 global Phase III trial showed AstraZeneca’s sonesitatug vedotin (Sone-Ve) demonstrated a statistically significant and highly clinically meaningful improvement in overall survival (OS) in 2nd- and later-line Claudin 18.2-positive advanced gastric cancers versus investigator’s choice of therapy. The trial included patients with locally advanced or metastatic gastric cancer, gastroesophageal junction (GEJ) cancer, or e...
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Genentech’s Divarasib Demonstrated Best-in-Class Efficacy, Advancing the Standard of Care in Previously Treated KRAS G12C-mutated Lung Cancer

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Divarasib demonstrated best-in-class efficacy in Phase III trial, advancing the standard of care in previously treated KRAS G12C-mutated lung cancer...
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TAGRISSO® (osimertinib) plus savolitinib reduced the risk of disease progression or death by 45% and the risk of death by 32% in MET-driven EGFR-mutated lung cancer after progression on TAGRISSO

WILMINGTON, Del.--(BUSINESS WIRE)--Positive results from the SAFFRON Phase III trial showed TAGRISSO® (osimertinib) plus savolitinib demonstrated a statistically significant and clinically meaningful improvement in both progression-free survival (PFS) and overall survival (OS) versus doublet platinum-based chemotherapy in patients with epidermal growth factor receptor-mutated (EGFRm) non-small cell lung cancer (NSCLC). Patients in the trial had tumors with high levels of MET overexpression or a...
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HIMS Deadline: Rosen Law Firm Urges Hims & Hers Health, Inc. (NYSE: HIMS) Stockholders to Contact the Firm for Information About Their Rights

NEW YORK--(BUSINESS WIRE)--Rosen Law Firm, a global investor rights law firm, reminds investors about a class action on behalf of purchasers of securities of Hims & Hers Health, Inc. (NYSE: HIMS) between August 4, 2025 and July 29, 2026. Hims describes itself as a company that “operates a health and wellness platform that connects consumers to licensed healthcare professionals.”For more information, submit a form, email attorney Phillip Kim, or give us a call at 866-767-3653.The Allegations:...
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Agenus Reports 72% of Patients with Locally Advanced dMMR Colon Cancer Had No Cancer Remaining at Surgery Following Six Weeks of BOT+BAL in Phase 2 NEOASIS Study at ESMO 2026

LEXINGTON, Mass.--(BUSINESS WIRE)--Agenus Inc. (Nasdaq: AGEN), a leader in immuno-oncology innovation, today announced early Phase 2 results from the mismatch repair-deficient (dMMR) colon cancer cohort of NEOASIS, an investigator-initiated pan-tumor study sponsored by the Netherlands Cancer Institute (NKI). NEOASIS is evaluating botensilimab (BOT), Agenus’ multifunctional, Fc-enhanced anti-CTLA-4 antibody, in combination with balstilimab (BAL), Agenus’ anti-PD-1 antibody, given before surgery...
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Genmab Announces Updated Follow-Up Analyses from Phase 2 Study of Petosemtamab Demonstrate Meaningful Objective Response Rates in Patients with Metastatic Colorectal Cancer

COPENHAGEN, Denmark--(BUSINESS WIRE)--Genmab A/S (Nasdaq: GMAB) today announced updated follow-up analyses from a Phase 2 trial evaluating petosemtamab, an investigational IgG1-bispecific antibody targeting the epidermal growth factor receptor (EGFR) and leucine-rich repeat containing G-protein-coupled receptor 5 (LGR5), in combination with FOLFOX or FOLFIRI in patients with metastatic colorectal cancer (mCRC). At a median follow-up of 5.9 months in the first-line (1L) setting and 7.1 months in...
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BeOne、「ESMO 2026」で難治性肝がん・肺がんに関する説得力のあるデータを発表

カリフォルニア州サンカルロス--(BUSINESS WIRE)--(ビジネスワイヤ) -- BeOne Medicines Ltd.(Nasdaq:ONC、HKEX:06160、SSE:688235)は、グローバルなオンコロジー企業であり、重点を置く固形腫瘍領域で開発する複数の差別化された治験薬について、「欧州臨床腫瘍学会(ESMO)2026年大会」(10月23~27日、マドリード)で新たなデータを発表しました。発表は消化器がん、肺がん、乳がんに及び、BeOneの固形腫瘍事業が勢いを増していることを示しています。 BeOneの固形腫瘍部門最高医学責任者であるマーク・ラナサ医学博士・哲学博士は、次のように述べています。 「ESMOでは、疾患の生物学的特性に応じて適切なモダリティーを選択するという当社の戦略が、意義ある臨床的進展につながっていることを示しています。当社のGPC3×4-1BB二重特異性抗体は、前治療歴の多い肝細胞がん(HCC)患者において、より長期の追跡でも引き続き良好な忍容性を示し、持続的な活性が認められています。また、当社の脳透過性PRMT5阻害薬とCEA標的ADCの初...