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Displaying Results 1426-1450 of 2013 "'MG'"

Dec 11, 2025, 08:00 ET HanchorBio Announces Oral Presentation of HCB101 at the ESMO Immuno-Oncology Congress 2025

cytopenia-sparing safety across 12 cohorts up to 36 mg/kg QWNo bleeding events or immune-related toxicities, with the majority of treatment-related adverse events being Grade 1-2Linear PK (T1/2 ~3 days) with receptor occupancy (RO) >99% at ≥8 mg/kgDurable antitumor activity,

More news about: HanchorBio Inc.


Dec 11, 2025, 07:07 ET Odyssey Functional Energy Expands Across Major U.S. Airports Nationwide with CIBO Express Deal

ingredients and no added sugar. With bold, craveable flavors, Odyssey provides clean, functional energy without the crash, available in both 222mg and 85mg caffeine formats to power whatever the day demands. Odyssey products are Non-GMO, Vegan, Gluten-Free, Kosher, and made with real fruit juice.Odyssey

More news about: Odyssey Functional Energy


Dec 11, 2025, 07:00 ET Biohaven Presents Clinical Safety and Efficacy Data for BHV-1510, a Next-Generation Trop2 Antibody Drug Conjugate in Combination with Cemiplimab at the 2025 European Society for Medical Oncology (ESMO) Immuno-Oncology Congress

stomatitis (Grade 3) at the 2.75 mg/kg Q3W dose. As of the clinical cutoff date, a total of 31 participants were treated with the combination of BHV-1510 and cemiplimab, with BHV-1510 doses ranging from 2-2.75 mg/kg Q3W and 1.25-1.5 mg/kg D1D8Q3W. Cemiplimab was given at 350 mg Q3W.Across all doses

More news about: Biohaven Ltd.


Dec 11, 2025, 06:45 ET Lilly's triple agonist, retatrutide, delivered weight loss of up to an average of 71.2 lbs along with substantial relief from osteoarthritis pain in first successful Phase 3 trial

randomized to retatrutide initiated treatment with 2 mg once weekly and increased the dose in a step-wise approach every four weeks until reaching the target dose of 9 mg (via steps at 2 mg, 4 mg and 6 mg) or 12 mg (via steps at 2 mg, 4 mg, 6 mg and 9 mg).The initial TRIUMPH Phase 3 global registrational

More news about: Eli Lilly and Company


Dec 10, 2025, 12:53 ET Detox Gallery Presents "I Grieve Different" -- A Month-Long Art Exhibition Exploring Grief, Healing, and Collective Humanity

THC/CBD-infused beverages provided by Ayrloom & TBD.Community & Wellness Programming: The month includes soundbath meditation sessions with MG Jarrett, a yoga and end-of-year journaling workshop, and a vision-boarding session for 2026 led by Artgurl, a women-powered creative organization specializing

More news about: DETOX GALLERY


Dec 10, 2025, 09:30 ET Lawmakers and Advocates Call on Pennsylvania to become the next state to enact water quality management reforms to prevent spread of Legionella and Legionnaires' Disease

include:Public Water System Requirements:Maintain minimum detectable disinfectant levels (0.5 mg/L for chlorine; 1.0 mg/L for chloramine).Develop a distribution system maintenance plan to mitigate the risk of Legionella bacteria.Records

More news about: Prevent Legionnaires'


Dec 10, 2025, 09:00 ET NEW RESEARCH SHOWS RO HELPS PATIENTS ACHIEVE WEIGHT LOSS AND SAFETY OUTCOMES CONSISTENT WITH CLINICAL TRIALS

median baseline body mass index (BMI) of 32.3 kg/m² (IQR 30.2-35.5) and baseline median weight of 94.3 kg. At 68 weeks, 52.1% of patients were on a 2.4 mg dose of semaglutide.ResultsAmong 655 participants (445 women and 210 men), the average body weight reduction was 16.6% (SD 7.5;

More news about: Ro


Dec 10, 2025, 07:00 ET Consumers report feeling lighter, more motivated, mindful, and happier with Montoloeder's Metabolaid® weight-control formulation

The US-based consumer study drew the opinions of 112 adult participants who took a 500mg daily dose of the botanical supplement for a period of eight weeks. They also completed a self-assessment questionnaire at the end of each week to document

More news about: Monteloeder, S.L.


Dec 10, 2025, 00:47 ET Kapture CX Reports Sustained Profitability, 80% YoY Growth; Eyes 2.5× Expansion Over Next 12 Months

profitable foundation, robust growth trajectory, and differentiated vertical-first full-stack AI strategy backed by marquee clients like BigBasket, Tata 1mg, Aditya Birla Capital, Coca-Cola, Reliance, and many more. Kapture CX is set to redefine enterprise employee-experience automation for both India and

More news about: Kapture CX


Dec 09, 2025, 16:00 ET Cirius Therapeutics to Highlight Cardiometabolic Benefits of CIR-0602K at Global Cardiovascular Clinical Trialists (CVCT) Forum 2025

InflammationReduced high-sensitivity C-reactive protein (hsCRP) in participants with hsCRP above 3 mg/L at baseline by approximately 40%; person with hsCRP >3 mg/L are at high risk for future cardiovascular events. Lipid Profile and other

More news about: Cirius Therapeutics


Dec 09, 2025, 11:38 ET El Grupo Menarini presenta datos de la combinación de fase 2 de Elacestrant (ORSERDU®) en cáncer de mama

Elacestrant 345 mg QD + Everolimus 7,5 mg QD (n=50) Elacestrant 345 mg QD

More news about: Menarini Industrie Farmaceutiche Riunite


Dec 09, 2025, 09:49 ET 메나리니 그룹, 2025 샌안토니오 유방암 심포지엄에서 엘라세스트란트(ORSERDU)®의 ER+, HER2- 전이성 유방암(mBC) 환자 대상 2상 병용 요법 데이터 발표

엘라세스트란트 345mg 1일 1회+ 에버로리무스 7.5mg 1일 1회(n=50)엘라세스트란트 345mg 1일 1회

More news about: Menarini Industrie Farmaceutiche Riunite


Dec 09, 2025, 09:00 ET Clinical Trial Shows Pycnogenol® Significantly Relieves Lipedema Symptoms and Improves Quality of Life in Women

Pycnogenol® in managing the condition. Participants were monitored over a 60-day period, with half receiving Pycnogenol® (50 mg, three times daily) and half receiving a placebo.Researchers evaluated quality of life, body composition and symptom severity at the start,

More news about: Horphag Research (USA) Inc.


Dec 09, 2025, 07:44 ET Unprecedented results from the Phase 3 MajesTEC-3 study support TECVAYLI® plus DARZALEX FASPRO® as a potential standard of care as early as second line for patients with relapsed/refractory multiple myeloma

at Week 2 or subsequent infusions. In EQUULEUS, patients receiving combination treatment (n=97) were administered the first 16 mg/kg dose at Week 1 split over two days, ie, 8 mg/kg on Day 1 and Day 2, respectively. The incidence of any grade infusion-related reactions was 42%, with 36% of patients experiencing

More news about: Johnson & Johnson


Dec 09, 2025, 07:30 ET Novel Agent Ianalumab Added to Standard Therapy Extends Time to Treatment Failure in Patients with Previously Treated Immune Thrombocytopenia

weeks. In addition, patients were randomly assigned to receive four once-monthly infusions of a lower dose of ianalumab (3 mg per kilogram of body weight), a higher dose ianalumab (9 mg per kilogram), or a placebo.  The study's primary endpoint was time to treatment failure, defined as elapsed time

More news about: American Society of Hematology


Dec 09, 2025, 07:30 ET Lilly's Jaypirca (pirtobrutinib) significantly improved progression-free survival, reducing the risk of progression or death by 80%, versus chemoimmunotherapy in patients with treatment-naïve CLL/SLL

lymphoma (MCL) and chronic lymphocytic leukemia (CLL).2,3 Jaypirca is a U.S. FDA-approved oral prescription medicine, 100 mg or 50 mg tablets taken as a once-daily 200 mg dose with or without food until disease progression or unacceptable toxicity.About Chronic Lymphocytic Leukemia/Small

More news about: Eli Lilly and Company


Dec 09, 2025, 05:00 ET Dizal Showcases its Strong Hematology Pipeline with New Data from Golidocitinib and Birelentinib at ASH 2025

Golidocitinib 75mg daily with CHOP, followed by 150mg maintenance after CHOP, showed an ORR of 94.1% and a CR rate of 64.7%. By the data cutoff date, 85% of patients remained on treatment.Golidocitinib 150mg daily with CHOP, followed by 150mg maintenance after CHOP, showed an

More news about: Dizal Pharmaceutical


Dec 08, 2025, 19:00 ET Innovent Announces PECONDLE® (Picankibart Injection) Phase 3 Study (CLEAR-2) Meets Endpoints, Delivering Superior Long-Term Management Solution for Moderate-to-Severe Psoriasis

maintained in both 100 mg and 200 mg maintenance groups, whereas the corresponding withdrawal groups exhibited median efficacy durability of 20.4 weeks and 24.6 weeks (32.4 weeks and 36.6 weeks post-last dose of picankibart), respectively. Maintenance treatment with picankibart 100 mg and 200 mg significantly

More news about: Innovent Biologics


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