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Werewolf Therapeutics to Participate in the BIO International Convention
GlobeNewswire News Room· 2025-06-12 12:00
WATERTOWN, Mass., June 12, 2025 (GLOBE NEWSWIRE) -- Werewolf Therapeutics, Inc. (the “Company” or “Werewolf”) (Nasdaq: HOWL), an innovative biopharmaceutical company pioneering the development of conditionally activated therapeutics engineered to stimulate the body’s immune system for the treatment of cancer and other immune-mediated conditions, today announced Randi Isaacs, M.D., Chief Medical Officer, will participate in a panel discussion at the upcoming BIO International Convention taking place June 16- ...
X @Elon Musk
Elon Musk· 2025-06-12 08:06
RT Mario Nawfal (@MarioNawfal)🇪🇺EUROPE’S RAPE STATS: THE NUMBERS THEY DON’T WANT YOU TO TALK ABOUTNorthern Ireland’s police said foreign nationals were 5.36x more likely to commit stranger rape than locals from 2019–2023.Sweden? 75% of stranger rapes were by non-Europeans - 22x the rate of Europeans.Finland? Migrants from Africa and the Middle East had 10x higher rates, even after controlling for income and education.Norway even had to organize courses for migrants to teach them a simple rule: “To force som ...
Molecular Partners presents positive data from ongoing Phase 1/2a trial of MP0533 in AML at EHA 2025
Globenewswire· 2025-06-11 20:00
Three of eight evaluable patients with R/R AML responded after cycle 1 in ongoing cohort 8, including 1 patient with ongoing response beyond 6 monthsAcceptable safety profile across all cohorts, including in cohort 8 with steeper step-up dosingData support further dose optimization to maximize therapeutic benefit of MP0533, with dosing in cohort 9 now ongoing ZURICH-SCHLIEREN, Switzerland and CONCORD, Mass., June 11, 2025 (GLOBE NEWSWIRE) -- Ad hoc announcement pursuant to Art. 53 LR Molecular Partners AG ( ...
Zymeworks(ZYME) - 2025 FY - Earnings Call Transcript
2025-06-11 19:00
Zymeworks (ZYME) FY 2025 Conference June 11, 2025 02:00 PM ET Speaker0 Good afternoon, everyone. Thanks so much for being here. My name is Laura Khan. I'm a Vice President in our Healthcare Investment Banking Group. And I'm joined today by Ken Galbraith, CEO of ZymWorks. Ken, thanks so much for being here. Let's go ahead and dive right in. It's of course been an exciting year at ZymWorks. A ton of progress with BTC approval in November for Zahira, and significant progress made on continuing to advance the p ...
Silo Pharma Secures Biomarker Patent for Novel PTSD Therapeutic SPC-15 as Clinical Trial Nears
Globenewswire· 2025-06-11 13:00
SARASOTA, FL, June 11, 2025 (GLOBE NEWSWIRE) -- Silo Pharma, Inc. (Nasdaq: SILO) (“Silo” or the “Company”), a developmental stage biopharmaceutical company focused on novel therapeutics and drug delivery systems, today announced that the U.S. Patent and Trademark Office (USPTO) had issued a Notice of Allowance for U.S. Patent Application No. 17/954,858 (titled “Biomarkers for Efficacy of Prophylactic Treatments Against Stress-Induced Affective Disorders”) that Silo licenses from Columbia University. The to ...
Will Merck's Keytruda Continue to Drive Growth Amid Looming LOE?
ZACKS· 2025-06-10 14:50
Core Insights - Merck (MRK) has over six blockbuster drugs, with Keytruda being the primary revenue driver, accounting for approximately 50% of pharmaceutical sales [1][9] - Keytruda's sales are increasing due to its rapid adoption in early-stage non-small cell lung cancer (NSCLC) and continued strong performance in metastatic indications [2] - There are concerns regarding Merck's heavy reliance on Keytruda, especially with the impending loss of exclusivity in 2028, prompting the need for diversification [3] Sales and Growth - Keytruda generated sales of $7.21 billion in Q1 2025, reflecting a 6% year-over-year growth, with an estimated compound annual growth rate (CAGR) of 5.4% over the next three years [7][9] - Merck is exploring innovative strategies to sustain Keytruda's growth, including combinations with LAG3 and CTLA-4 inhibitors, and a partnership with Moderna for a personalized mRNA therapeutic cancer vaccine [5][9] Competitive Landscape - Competitive pressure for Keytruda may increase, particularly with Summit Therapeutics' ivonescimab showing promising results in a phase III study, which could challenge Keytruda's market position [4] Future Strategies - Merck is developing a subcutaneous formulation of Keytruda to potentially extend its patent life, with an FDA decision expected in September [6] - The company is also banking on the recently launched pulmonary arterial hypertension (PAH) drug Winrevair to support revenue after Keytruda's exclusivity ends [7] Valuation and Market Performance - Merck's shares have decreased by 19.6% this year, contrasting with a 0.3% increase in the industry [8] - From a valuation perspective, Merck's price/earnings ratio stands at 8.55, which is lower than the industry average of 15.12 and its own 5-year mean of 12.89 [10]
Ashvattha Therapeutics to Present Phase 2 DME and Wet AMD Data at Clinical Trials at the Summit and MaculArt
GlobeNewswire News Room· 2025-06-10 12:01
Ashvattha will present Phase 2 data on migaldendranib, a subcutaneous therapy for DME and wet AMD, which could offer a more patient-friendly alternative to current injection-based treatments Company is exploring new technology to normalize VEGF expression, potentially enhancing both safety and efficacy of treatments for retinal and other diseases REDWOOD CITY, Calif., June 10, 2025 (GLOBE NEWSWIRE) -- Ashvattha Therapeutics (“Ashvattha”), a clinical-stage company advancing a new class of nanomedicine therap ...
Vanda Pharmaceuticals Announces First Patient Dosed in a Trial Evaluating VCA-894A in Charcot-Marie-Tooth disease Type 2S
Prnewswire· 2025-06-10 12:00
WASHINGTON, June 10, 2025 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced the first dose in the first-in-human clinical trial to evaluate the safety and tolerability of VCA-894A, an antisense oligonucleotide (ASO) therapeutic, for a patient with a rare variant in the IGHMBP2 gene causing Charcot-Marie-Tooth disease Type 2S (CMT2S). VCA-894A is being developed for a patient who was first diagnosed at the age of 5 with a rare subtype of CMT disease known as CMT2S.1 CMT2S is a ...
OPKO Health’s ModeX Therapeutics Announces Formation of Scientific Advisory Board with Leaders at the Forefront of Immunology and Oncology Drug Development
Globenewswire· 2025-06-09 12:00
Will provide expertise across ModeX’s portfolio of next generation multispecific antibodies for complex diseases involving the immune system, including cancer ModeX’s promising immunology pipeline includes first-in class drugs with two assets in ongoing clinical trials and multiple pre-IND assets to enter clinical trials WESTON, Mass., June 09, 2025 (GLOBE NEWSWIRE) -- ModeX Therapeutics Inc., an OPKO Health company (NASDAQ: OPK), today announced the creation of a Scientific Advisory Board to provide counse ...
Ionis Pharmaceuticals (IONS) Update / Briefing Transcript
2025-06-05 22:30
Summary of Ionis Pharmaceuticals (IONS) Update / Briefing June 05, 2025 Company Overview - **Company**: Ionis Pharmaceuticals (IONS) - **Industry**: Biotechnology, specifically focusing on RNA-targeted therapeutics Core Points and Arguments 1. **Strategic Shift**: The company has transitioned from a partnership-focused model to a fully integrated biotechnology company, aiming to commercialize its own drugs and enhance shareholder value [3][4][5] 2. **Pipeline Development**: Ionis has a robust pipeline with 10 drugs in phase three development, half of which are wholly owned, targeting both rare and prevalent diseases, particularly in neurology and cardiovascular areas [12][13][59] 3. **Recent Approvals**: The company has launched several transformational medicines, including Trigolsa for familial chylomicronemia syndrome and is anticipating further approvals for drugs targeting hereditary angioedema and severe hypertriglyceridemia [7][16][28][40] 4. **Technological Advancements**: Ionis has expanded its platform technology, including new chemistries for antisense drugs and siRNA, to strengthen its competitive position in RNA-based therapeutics [8][9][49] 5. **Commercial Success**: The launch of Trigolsa generated over $6 million in revenue in its first quarter, exceeding expectations, indicating strong market uptake and physician engagement [17][19] 6. **Upcoming Milestones**: The company expects significant data readouts and potential approvals in the near future, including phase three results for olazarsen and zilgarnarsen, which could lead to additional product launches [56][57] Important but Overlooked Content 1. **Patient Needs**: There is a high unmet need for effective treatments in conditions like hereditary angioedema, with surveys indicating that a significant percentage of patients are dissatisfied with current therapies [30][31] 2. **Market Dynamics**: The company is strategically positioned to capture market share in both rare and prevalent disease segments, leveraging its first-mover advantage in several therapeutic areas [28][60] 3. **Regulatory Engagement**: Ionis has maintained a positive relationship with the FDA, with no disruptions reported in the review timeline for upcoming drug approvals [64][65] 4. **Research and Development**: The company is actively advancing multiple drug candidates each year, focusing on cardiology and neurology, with plans to initiate clinical trials for new targets [66][70] Financial Outlook - **Revenue Potential**: Ionis anticipates over $5 billion in potential annual peak product revenue from its wholly owned and partnered pipelines, with significant contributions expected from upcoming launches and approvals [59][61] This summary encapsulates the key developments and strategic direction of Ionis Pharmaceuticals, highlighting its commitment to innovation and market leadership in RNA-targeted therapeutics.