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ADC Therapeutics Announces Updated Data from LOTIS-7 Clinical Trial Presented at the European Hematology Association 2025 Congress
Prnewswire· 2025-06-12 10:30
Core Insights - ADC Therapeutics announced promising results from the LOTIS-7 Phase 1b trial, showing a 93.3% overall response rate (ORR) and an 86.7% complete response (CR) rate in patients with relapsed or refractory diffuse large B-cell lymphoma (r/r DLBCL) treated with ZYNLONTA® and glofitamab [1][3][4] Efficacy Data - Among 30 efficacy evaluable patients, 28 achieved an overall response, with 26 achieving complete responses [3] - 25 out of 26 patients who achieved CR remained in CR at the data cut-off [1][3] - Median time to CR was 80 days for the 120 µg/kg dose and 42 days for the 150 µg/kg dose [3] - 12 patients converted from stable disease or partial response to CR over time [3] - Of 6 patients previously treated with CAR-T, 5 achieved CR [3] Safety Profile - The combination treatment was generally well tolerated, with no dose-limiting toxicities (DLTs) reported [3] - Among 41 safety evaluable patients, the most common grade 3 or higher treatment-emergent adverse events (TEAEs) included neutropenia (24.4%), anemia (9.8%), and increased liver enzymes [3] - Cytokine release syndrome (CRS) was observed in 23.8% of patients at the 150 µg/kg dose, all Grade 1, while 55% experienced CRS at the 120 µg/kg dose [3] Study Expansion - The company is expanding enrollment for the LOTIS-7 trial to 100 patients at the 150 µg/kg dose of ZYNLONTA [1][4] - The updated data will be presented at the European Hematology Association 2025 Congress and the 18th International Conference on Malignant Lymphoma [4] About ZYNLONTA - ZYNLONTA is a CD19-directed antibody drug conjugate (ADC) approved for treating adult patients with r/r large B-cell lymphoma after two or more lines of systemic therapy [9][13] - The drug works by binding to CD19-expressing cells and delivering a potent payload that leads to tumor cell death [8]
Compound Your Retirement With These 5 Monthly Dividend REITs
Seeking Alpha· 2025-06-11 11:00
Group 1 - The article discusses insights gained from a meeting with Bill Ackman regarding Howard Hughes Holdings [1] - The company offers a comprehensive research platform called iREIT®, which includes data on various investment vehicles such as REITs, mREITs, Preferreds, BDCs, MLPs, ETFs, Builders, and Asset Managers [1] - iREIT® Tracker provides data on over 250 tickers, including quality scores, buy targets, and trim targets [1] Group 2 - A new Ratings Tracker named iREIT Buy Zone has been introduced to assist members in screening for value [2] - The company is offering a 2-week free trial for its services, which includes access to the Ratings Tracker [4] - The offer also includes a free book as part of the promotional package [4]
Agree Realty: Add The King Of Retail REITs To Your Portfolio
Seeking Alpha· 2025-06-10 20:33
David A. Johnson is founder and principal of Endurance Capital Management, a New Jersey Limited Liability Company. As an investor entrepreneur, David invests in stocks, bonds, options, ETFs, REITs, real estate, closed end funds and alternative investment funds such as hedge funds and private credit. With over 30 years’ experience in investing, David holds a Master of Science (MS) Degree in Finance, with a concentration in Investment Analysis, from Boston University, a Certificate in Financial Planning, and ...
Agree Realty: Crown Jewel Of My REIT Portfolio On Hold
Seeking Alpha· 2025-06-10 10:17
Core Insights - Agree Realty (NYSE: ADC) is gaining relevance in the industry due to its consistent delivery of strong results and dividends [1] Group 1: Company Performance - ADC has successfully attracted investors by providing reliable financial performance, including dividends [1] - The company is positioned as a solid option for dividend investing, which is viewed as an accessible path to financial freedom [1] Group 2: Analyst Background - The analyst has extensive experience in M&A and business valuation, having evaluated numerous businesses and participated in various transactions [1] - The focus of the analyst's work spans multiple sectors, including tech, real estate, software, finance, and consumer staples, which are also reflected in their investment portfolio [1]
Defence Therapeutics Receives USPTO Allowance for Patent Application Covering Next-Gen ADC Technology
Newsfile· 2025-06-09 07:15
Core Insights - Defence Therapeutics Inc. has received a Notice of Allowance from the USPTO for its U.S. patent application covering next-generation antibody-drug conjugate (ADC) technology, which includes broad composition-of-matter claims for therapeutically active ADCs [1][2] - The allowed patent application (no. 18/351,291) will potentially grant the company market exclusivity for its proprietary second-generation Accum®-based ADCs until 2043 [2][4] - The company has an established patent portfolio for its Accum® technology, with granted patents in the U.S., Japan, Australia, and Israel, and pending applications in Canada and Europe [3][4] Company Overview - Defence Therapeutics is a clinical-stage biotechnology company focused on developing next-generation ADC products using its proprietary Accum® technology, which enhances the precision delivery of ADCs to target cells [5] - The Accum® technology aims to increase the efficacy and potency of cancer treatments [5]
3 Top Real Estate Dividend Stocks to Buy for Super Easy Passive Income in June
The Motley Fool· 2025-06-04 01:12
Core Viewpoint - Investing in real estate, particularly through Real Estate Investment Trusts (REITs), offers a straightforward way to generate passive income with minimal effort [2][16] Group 1: Agree Realty - Agree Realty focuses on acquiring and developing high-quality retail properties leased to financially strong retailers, with 68.3% of its rent coming from tenants with investment-grade credit [4][6] - The company has a monthly dividend yield of over 4% and has grown its payout at a 5.5% compound annual rate over the past decade [5][6] - Agree Realty maintains a low dividend payout ratio of 72% of its adjusted funds from operations, allowing for cash retention for further investments [6] Group 2: Prologis - Prologis is one of the largest REITs globally, specializing in logistics properties leased under long-term contracts, providing steady rental income [8][10] - The company benefits from strong demand for warehouse space, allowing for new leases at higher market rates, which is expected to drive net operating income growth [9][11] - Prologis has delivered a 13% compound annual dividend growth over the past five years, outperforming the S&P 500 and the REIT sector average [11] Group 3: Mid-America Apartment Communities - Mid-America Apartment Communities is a major apartment landlord in the U.S., owning over 104,000 apartment homes, primarily in the Sun Belt region [12][14] - The REIT has a history of 125 consecutive quarterly dividends, demonstrating a strong record of dividend stability and growth [13] - The company is investing $657.3 million into properties currently in the lease-up phase and plans to spend another $851.5 million on additional development projects [14][15] Group 4: Investment Opportunities - Top REITs like Agree Realty, Prologis, and Mid-America Apartment Communities possess high-quality real estate portfolios and strong financial profiles, enabling them to pay lucrative and growing dividends [16]
2025 ASCO Presentation: Innovent Biologics Announces Updated Data of IBI354 (Novel anti-HER2 ADC) From the Phase 1/2 Clinical Study in Advanced Ovarian Cancer, Breast Cancer and Other Solid Tumors
Prnewswire· 2025-06-03 01:00
Core Viewpoint - Innovent Biologics has presented promising clinical data for IBI354, a HER2 monoclonal antibody-camptothecin derivative conjugate, at the 2025 ASCO Annual Meeting, highlighting its potential in treating advanced solid tumors, particularly in ovarian and breast cancer [1][2]. Group 1: Clinical Data and Efficacy - IBI354 has shown promising anti-tumor efficacy and favorable safety profiles across multiple solid tumors, indicating its potential as a new generation of ADC therapies characterized by high potency and low toxicity [2][5]. - The Phase 1/2 clinical study enrolled 368 participants with advanced solid tumors, with a median follow-up duration of 11.5 months and a median treatment duration of 27.0 weeks [3]. - In the ovarian cancer cohort, IBI354 achieved an objective response rate (ORR) of 55.0% and a disease control rate (DCR) of 90.0% at a dose of 12mg/kg Q3W, with a median progression-free survival (PFS) of 7.1 months [6][7]. Group 2: Safety Profile - IBI354 demonstrated an excellent safety profile, with a low incidence of treatment-related adverse events (TRAEs) and no dose-limiting toxicities (DLTs) observed at escalated doses [4][7]. - The most common TRAEs included anemia, nausea, and decreased white blood cell count, with only 1.9% of patients experiencing interstitial lung disease [7]. Group 3: Future Development and Strategic Positioning - The Phase 3 study of IBI354 in platinum-resistant ovarian cancer has been initiated, indicating the company's commitment to further validating the long-term benefits of this treatment [8]. - Innovent is advancing its strategic layout in the ADC field, with plans for additional clinical studies and investments in next-generation ADC molecules to address unmet clinical needs [8][10].
ASCO 2025 Oral Presentation: Innovent Biologics Announces Updated Data of IBI343 (Novel Anti-CLDN18.2 ADC) From the Phase 1 Clinical Study in Patients with Advanced Pancreatic Cancer
Prnewswire· 2025-06-03 01:00
Core Viewpoint - Innovent Biologics has presented promising Phase 1 study results for IBI343, a novel anti-CLDN18.2 ADC, for advanced pancreatic cancer, indicating its potential as a breakthrough therapy in a challenging-to-treat malignancy [2][4]. Company Overview - Innovent Biologics is a leading biopharmaceutical company founded in 2011, focused on developing high-quality medicines for various diseases, including oncology, cardiovascular, and autoimmune disorders [10]. - The company has launched 15 products and has multiple assets in various stages of clinical trials, partnering with over 30 global healthcare companies [10]. Clinical Study Results - The Phase 1 study of IBI343 showed a confirmed overall objective response rate (cORR) of 22.7% and a disease control rate (DCR) of 81.8% in patients with CLDN18.2 expression treated at a 6mg/kg dose [6]. - The median progression-free survival (mPFS) was reported at 5.4 months, and the median overall survival (mOS) was 9.1 months, with variations based on prior treatments [6]. - The safety profile of IBI343 was favorable, with a low rate of gastrointestinal toxicity and no new safety signals reported [6]. Market Context - Pancreatic cancer is one of the most aggressive cancers, with a global 5-year survival rate of less than 10% and approximately 510,000 new cases and 467,000 deaths annually [3][4]. - The clinical options for second-line treatment of advanced pancreatic cancer are limited, highlighting the urgent need for effective therapies [4]. Regulatory Designations - IBI343 has received Breakthrough Therapy Designation (BTD) from China's National Medical Products Administration (NMPA) and Fast Track Designation (FTD) from the U.S. Food and Drug Administration (FDA) [2][9].
5 Monthly Dividend REITs To Retire With Passive Income
Seeking Alpha· 2025-06-02 12:15
Group 1 - Real estate is often viewed as a lucrative investment for generating passive income through monthly rent payments from tenants [1] - The common perception suggests minimal effort is required from landlords to manage properties [1] - The article hints at a discrepancy between perception and reality in real estate investment [1]
Lilly presents first clinical data for its investigational, next-generation FRα targeting ADC in platinum-resistant ovarian cancer at the 2025 ASCO Annual Meeting
Prnewswire· 2025-06-02 12:00
Core Insights - Eli Lilly and Company announced promising Phase 1 data for its folate receptor alpha (FRα) antibody-drug conjugate (ADC) LY4170156, showing a preliminary overall objective response rate (ORR) of 55% in women with heavily pre-treated platinum-resistant ovarian cancer [1][2][3] Group 1: Clinical Data and Efficacy - The study enrolled 95 participants with high-grade serous ovarian cancer, with a median of five prior systemic regimens [2][3] - Among the 95 patients, 51% had tumors with FRα expression less than 75%, while 34% had expression of 75% or higher [2] - The ORR was 45% in 58 efficacy-evaluable patients, with a disease control rate of 74% [3] Group 2: Safety Profile - The most common treatment-emergent adverse events included nausea (64%), anemia (40%), fatigue (32%), vomiting (32%), diarrhea (28%), and neutropenia (27%) [3] - No maximum tolerated dose has been established, and treatment-emergent neuropathy and ocular toxicity have not been observed to date [3] Group 3: Future Directions - Based on the results, the company aims to advance LY4170156 into registrational Phase 3 clinical trials [4] - The ADC is designed to target FRα across expression levels with an improved therapeutic index, potentially benefiting a larger number of ovarian cancer patients [5]