Eli Lilly and Company (NYSE:LLY) is included among the 12 Best Long Term US Stocks to Buy Now. Eli Lilly (LLY) Gains Support From Daiwa and Goldman Sachs in Back-to-Back Calls On December 16, Daiwa analyst Narumi Nakagiri upgraded Eli Lilly and Company (NYSE:LLY) to Buy from Neutral and set a $1,230 price target on the stock. That move followed a similar call from Goldman Sachs earlier. On December 15, Goldman raised its price target on Eli Lilly to $1,145 from $951 and kept a Buy rating. Momentum aro ...

Core Insights - Viking Therapeutics is focused on developing therapies for metabolic and endocrine disorders, gaining attention in the anti-obesity drug sector with a promising product pipeline [1][6] - The company's dual GLP-1/GIP agonist, VK2735, is in late-stage trials and has attracted interest from major pharmaceutical companies [2][6] - VK2735 has shown impressive efficacy but faces challenges, including a 20% discontinuation rate in phase 2 trials due to adverse events [3][6] Company Pipeline - VK2735 is available in both oral and subcutaneous forms, making it an attractive acquisition target [2] - The oral version of VK2735 has achieved unmatched double-digit weight loss within just 13 weeks, positioning Viking as a potential leader in the oral obesity drug market [4] - Viking is also expanding its pipeline with a promising amylin agonist program [4] Financial Overview - Currently, VKTX is trading at $34.52, reflecting a slight increase of 0.63% [5] - The stock has a market capitalization of approximately $3.9 billion and a strong cash reserve of $714 million [5][6] - Despite the strong cash position, the company faces risks such as potential dilution and high costs associated with advancing its pipeline [5][6]

It has been a very good year for the British pharmaceutical stock GSK plc ( GSK ), which is up by ~46% YTD. This far exceeds the performance of the healthcare sector, as evident from the 13.5% returns on theManika is a macroeconomist with over 20 years of experience in industries including investment management, stock broking, investment banking. She also runs the profile Long Term Tips [LTT], which focuses on the generational opportunity in the green economy. Her investing group, Green Growth Giants, takes ...

SAN DIEGO, Dec. 18, 2025 (GLOBE NEWSWIRE) -- Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX), today announced that that Scott Struthers, Ph.D., Founder and Chief Executive Officer of Crinetics, will present at the 44th Annual J.P. Morgan Healthcare Conference being held in San Francisco, CA on Tuesday, January 13, 2026 at 9:45 a.m. Pacific Time. To access the live audio-only webcast, click here. The archived webcast will also be accessible on the Events & Presentations page in the Investors section of the Cr ...

Core Insights - Galapagos NV announced positive topline results from two Phase 3-enabling studies for GLPG3667, a selective TYK2 inhibitor, showing significant clinical benefits in dermatomyositis but not in systemic lupus erythematosus [1][3][4] Dermatomyositis Study (GALARISSO) - The GALARISSO study met its primary endpoint, demonstrating a statistically significant clinical benefit with a Total Improvement Score (TIS) of 14.26 at Week 24 (p=0.0848) compared to placebo [2][4] - GLPG3667 also showed meaningful improvements on secondary endpoints, including TIS20, TIS40, TIS60, and m-CDASI-A, with a favorable safety profile throughout the 24-week treatment period [2][4] Systemic Lupus Erythematosus Study (GALACELA) - In the GALACELA study, GLPG3667 did not achieve statistical significance for the primary endpoint (SLE responder index SRI-4) at Week 32, despite showing numerical improvements on several secondary endpoints, particularly skin-related outcomes [3][4] - The ongoing GALACELA study is expected to provide final Week 48 data in the second quarter of 2026, which will be crucial for assessing the overall evidence and determining next steps for the SLE program [3][4] Strategic Development - The company plans to evaluate all strategic alternatives, including resuming its partnering process to accelerate GLPG3667's development in dermatomyositis and exploring opportunities in other severe autoimmune diseases [1][4][5] - Gilead has temporarily waived certain rights under their collaboration agreement, allowing Galapagos to pursue external partnership opportunities for GLPG3667 [5] Background on Diseases - Dermatomyositis (DM) is a rare autoimmune disorder characterized by severe muscle weakness and skin manifestations, with a high unmet need for effective treatments [9] - Systemic lupus erythematosus (SLE) is a chronic autoimmune disease affecting multiple organ systems, with current treatments often associated with partial efficacy and significant toxicities [10]

Let's get more now on the story. Pharma and biotech reporter Anukica Kim Constantino. Anukica, what's the story here.Is this pill going to be ready soon. >> Right. So, thanks for having me on today.So, basically the news today is that Lily has trial data showing that its obesity pill could be an effective maintenance treatment for people that want to preserve their weight loss but don't want to keep taking weekly injections like Wgoian Zepbound. So in this trial, they basically followed people that initiall ...

Let's get more now on the story. Pharma and biotech reporter Anukica Kim Constantino. Anukica, what's the story here.Is this pill going to be ready soon. >> Right. So, thanks for having me on today.So, basically the news today is that Lily has trial data showing that its obesity pill could be an effective maintenance treatment for people that want to preserve their weight loss but don't want to keep taking weekly injections like Wgoian Zepbound. So in this trial, they basically followed people that initiall ...

Core Viewpoint - Zhejiang Hai Zheng Pharmaceutical Co., Ltd. has received a new veterinary drug registration certificate for its product, Methylprednisolone Tablets (for dogs), which is classified as a Category V new veterinary drug, indicating compliance with relevant regulations and enhancing the company's strategic positioning in the veterinary medicine sector [1][4]. Group 1: New Veterinary Drug Information - The new veterinary drug is named Methylprednisolone Tablets (for dogs) and has been approved as a Category V new veterinary drug [1]. - The registration certificate number for the new veterinary drug is (2025) New Veterinary Drug Certificate No. 129 [1]. - The drug is developed by Zhejiang Hai Zheng Animal Health Products Co., Ltd. in collaboration with seven other companies [1]. Group 2: Drug Application and Use - Methylprednisolone Tablets (for dogs) are intended for the treatment of canine inflammatory and allergic diseases, and can be part of treatment regimens for conditions such as allergic or non-specific dermatitis, musculoskeletal diseases, and inflammation of the eyes/ears [1]. - The drug is effective for various inflammatory/allergic diseases that can be treated with glucocorticoids, including immune-mediated diseases [1]. Group 3: Market Position and Future Outlook - The approval of Methylprednisolone Tablets (for dogs) is expected to enhance the company's market competitiveness in the veterinary drug sector [4]. - The product is now ready for production and market launch, pending the acquisition of the veterinary product approval number, although it is noted that it will not have a significant short-term impact on the company's performance [4].

This article is published by Terry Chrisomalis, who runs the Biotech Analysis Central pharmaceutical service on Seeking Alpha Marketplace. If you like what you read here and would like to subscribe to, I'm currently offering a two-week free trial period for subscribers to take advantage of. My service offers a deep-dive analysis of many pharmaceutical companies. The Biotech Analysis Central SA marketplace is $49 per month, but for those who sign up for the yearly plan will be able to take advantage of a 33. ...

Core Viewpoint - Athira Pharma Inc. is making significant strides in its development pipeline by acquiring rights to lasofoxifene, a drug in a Phase 3 trial for metastatic breast cancer, which is expected to enhance its market position and growth potential [1][2]. Group 1: Acquisition Details - Athira has secured an exclusive global license (excluding Asia and certain Middle Eastern countries) from Sermonix Pharmaceuticals for the development and commercialization of lasofoxifene [2]. - As part of the agreement, Athira will issue a pre-funded warrant to purchase approximately 5.5 million shares at an exercise price of $0.001 per share, along with potential payments of up to $100 million based on commercialization or annual net sales milestones [3]. Group 2: Financing and Development Plans - The company announced a $90 million upfront financing through private placement of common stock and warrants, which could provide an additional $146 million if the warrants are exercised, aimed at supporting the development of lasofoxifene through key clinical and regulatory milestones [4]. - The net proceeds from the financing will be utilized for the development of lasofoxifene for treatment-resistant metastatic breast cancer, other clinical assets, and general corporate purposes [5]. Group 3: Market Performance - Following the announcement, Athira Pharma's stock surged by 74.49% to $7.22, reaching a new 52-week high, indicating strong market confidence in the company's future prospects [5].