Digital Asset DirectBiVictriX Therapeutics makes 'fundamental step forward'
BlueRush Inc.
Contact Details Proactive UK Ltd +44 20 7989 0813 uk@proactiveinvestors.com
January 22, 2023 07:55 AM Eastern Standard Time
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Digital Asset Direct
News ReleaseAgile Therapeutics: This BioPharma Firm Is Nimbly Solving Unmet Needs For Women
Agile Therapeutics, Inc.
By Johnny Rice, Benzinga Al Altomari, Chairman and CEO of Agile Therapeutics Inc (NASDAQ: AGRX), was recently interviewed by Benzinga. Agile Therapeutics says it is a women's healthcare company dedicated to fulfilling the unmet health needs of today’s women. Its products and product candidates are designed to provide women with contraceptive options that offer freedom from taking a daily pill, without committing to a longer-acting method. The company’s flagship product is Twirla® (levonorgestrel and ethinyl estradiol), a non-daily prescription contraceptive utilizing a transdermal system. Twirla is based on proprietary transdermal patch technology, called Skinfusion®, designed to allow drug delivery through the skin. Watch the full interview here: Agile Therapeutics is a women's healthcare company dedicated to fulfilling the unmet health needs of today’s women. Our product and product candidates are designed to provide women with contraceptive options that offer freedom from taking a daily pill, without committing to a longer-acting method. Our initial product, Twirla®, (levonorgestrel and ethinyl estradiol), a transdermal system, is a non-daily prescription contraceptive. Twirla is based on our proprietary transdermal patch technology, called Skinfusion®, which is designed to allow drug delivery through the skin. This post contains sponsored advertising content. This content is for informational purposes only and is not intended to be investing advice. Contact Details Matt Riley - Head of Investor Relations & Corporate Communications mriley@agiletherapeutics.com Company Website https://agiletherapeutics.com/
January 20, 2023 08:45 AM Eastern Standard Time
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News ReleaseKinspire Raises $3.6M to Reimagine Pediatric Occupational Therapy By Including Parents for Better Outcomes
Kinspire
Denver, CO — January 20, 2022 – Kinspire, the leading pediatric occupational therapy platform designed to pair expert therapists with parents, co-founded by Lily Baiser and Robert Seigel, today announced it has closed $3.6 million in seed funding. The round was co-led by Corazon Capital and Looking Glass Capital, with participation from Difference Partners, Great Oaks VC, Service Provider Capital, The Fund, Copper Wire Ventures, and Bradley Tusk. Launched in 2020, Kinspire provides a family-centered and value-based care model for pediatric occupational therapy to families of children with developmental delays and disabilities. Roughly 1 in 6 children in America are diagnosed with developmental delays or disabilities and can greatly benefit from services such as occupational therapy. However, long waitlists for evaluations, high costs of services, and inconvenient provider distribution produce accessibility and affordability constraints. Moreover, studies have repeatedly demonstrated that involving parents in their child's occupational therapy leads to better outcomes and faster progress. Despite this, traditional OT approaches do not always fully incorporate parent involvement. These constraints often lead to significant delays or a complete lack in children receiving critical pediatric therapeutic services, such as occupational therapy. “The current model for delivering development support services to children fails far too many kids. We have invested in Kinspire to accelerate its mission to make occupational therapy more accessible, affordable, and effective,” said Sam Yagan, Co-Founder & Managing Partner of Corazon Capital. In response, Kinspire has pioneered an entirely new approach to pediatric occupational therapy designed to empower parents to support their child's therapy at home and become an active member of the treatment team. This family-centered care model is in alignment with Harvard’s Center for the Developing Child and Early Intervention Programs. The Spiral Foundation conducted a 12-week study on the use of the Kinspire app for occupational therapy in pediatrics. Over 70% of parents reported that Kinspire made it easier to select activities for home therapy, and the study concluded that the app has preliminary potential as a tool for augmenting clinic-based services. Guided by Kinspire’s expert occupational therapists, children receive high-quality care and parents learn the skills, strategies, and techniques needed to help their child reach their full potential and reduce their own stress. By focusing on the unique needs and goals of each child, Kinspire provides the most effective and efficient care possible for the entire family unit. "As a parent who has personally gone through OT with my child, I have seen firsthand the benefits of being an active participant in the therapy process. That's why we have made it a cornerstone of our pediatric OT platform at Kinspire. This funding allows us to create high levels of collaboration between therapists and parents for better outcomes and faster progress for every child.” said Robert Seigel, CEO & Co-Founder of Kinspire. Unlike traditional occupational therapy, families who use Kinspire pay a monthly membership fee for Kinspire’s multimodal connection to their therapist. Families receive around-the-clock support from their Kinspire therapist with unlimited messaging services, a live 1:1 monthly session, daily parent education, and ongoing access to Kinspire’s mobile app and video library to monitor and measure progress. ABOUT KINSPIRE: Kinspire is the leading family-centered and value-based care model for pediatric occupational therapy on a mission to deliver the highest quality developmental care with better outcomes in less time. Currently providing services in Florida, California, Colorado, and Texas. Kinspire accepts FSA and HSA and is actively working to expand its list of insurance coverage providers to ensure its services are accessible to more children and families. For more information about Kinspire, please visit www.kinspirehealth.com Contact Details Christina Goldstein cgoldstein@tuskholdings.com Jennifer Mingucci Jennifer@KinspireApp.com Company Website https://www.kinspirehealth.com
January 20, 2023 08:15 AM Eastern Standard Time
News ReleaseMedica Group eyeing up "significant opportunity"
Medica Group PLC
Medica Group PLC (LSE:MGP) chief executive Dr Stuart Quin speaks to Proactive's Thomas Warner following the release of a 2022 trading update. He reveals more information about what he calls a "significant opportunity' for the Medica Group as it heads into another new year, and discusses where he believes the bulk of its growth will come from. Contact Details Proactive Proactive UK Ltd +44 20 7989 0813 uk@proactiveinvestors.com
January 20, 2023 07:05 AM Eastern Standard Time
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News ReleasePrescriptions Generated Three Times More Frequently on POC Mediums: Doceree 2022 Annual Report
Doceree
Point-of-Care (POC) channels have changed the dynamics of how life sciences brands interact with healthcare professionals (HCPs) which has led to script generation to become three times on POC than on other online mediums, Doceree has revealed in its annual report – Doceree 360 (2022 Edition). Doceree, a global platform building unprecedented solutions for HCP programmatic messaging with proprietary data tools, today released its annual report, compiled post analysis of more than 250 POC campaigns run on its platform over the last year. To drive prescriptions, it is crucial for life sciences brands to target HCPs while they tend to their patients, which is only on point-of-care channels, concludes the report. Doceree has pioneered initiatives to evolve the POC ecosystem with insightful learnings for life sciences brand marketers and platforms. A few months prior to the report launch, the company’s Founder and CEO Harshit Jain, MD launched a book on the subject with the goal of preparing marketers and point-of-care platforms for the next way to effectively reach and engage clinicians through online platforms. “The POC landscape is in its nascent stage and is evolving at a fast pace,” Jain said. “There is apparently a lack of standardization owing to limited availability of data points and metrics at this stage. “We are attempting to fill this gap by diving into the multiple POC campaigns we have executed on our platform in the past year to deduce some insightful learnings for marketers to take cognisance of,” he continued. “It will empower them to embrace data-driven strategies and personalize HCP communications with a deep understanding of online behavior patterns of providers based on real-time campaigns.” The other key findings in the report are: HCPs spend an average of six hours out of an average 11-hour workday on EHR Script lift is 32% higher in trigger-based messaging Cost per HCP is 17% less on POC than on other mediums Doceree gauged more than 21 million impressions served to more than 600,000 HCPs on its over 70-partner POC channels. Campaigns of around 100 advertisers - comprising consumer healthcare and medical devices companies, life sciences brands, hospitals, and diagnostics - run on a blend of POC channels, consisting of EHR, eRx, telemedicine, EHR apps, were taken into account. Brand campaigns for more than 190 specialties, including Primary Care, Cardiology, Oncology, Hematology, Nephrology, Gynaecology and Pulmonology, were studied as part of the research for the report findings. View the complete report by visiting: https://doceree.com/in/reports/doceree-360-2022-edition/ About Doceree Doceree is a global platform building unprecedented solutions for healthcare professional (HCP) programmatic messaging with proprietary data tools. It facilitates messaging between life sciences brands and HCPs through an extensive global network of digital endemic and point-of-care platforms to programmatically deliver personalized communications to HCPs and transparent marketing campaign metrics at scale. To learn more, visit doceree.com. Contact Details Kite Hill PR +91 70420 89805 doceree@kitehillpr.com Company Website https://doceree.com/us/
January 19, 2023 11:20 AM Eastern Standard Time
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News ReleaseOliver Inc. Acquires Tap Packaging + Design
Oliver Inc.
Oliver Inc. (“Oliver”) is pleased to announce that it has acquired Tap Packaging + Design. Tap Packaging is a leading manufacturer of custom folding cartons, serving customers in food and beverage, beauty, confection, health and wellness, and consumer goods markets. Based in Cleveland, Ohio, Tap Packaging will continue delivering design-forward packaging solutions from its current location. This partnership will enable Oliver to expand its product offerings and strengthen its position as the nation’s largest independent specialty packaging supplier. “We are thrilled to welcome the Tap team to the Oliver family,” said Dan Rodenbush, President/CEO of Oliver Inc. "Their diverse range of capabilities will allow us to expand our product offerings and enhance our overall service for our customers.” “Oliver and Tap Packaging share similar core values, and both companies have a passion for providing an exceptional customer experience,” added David Chilcote, Chairman of Tap Packaging. “Partnering with Oliver increases our capacity, provides redundancy, and allows us to better leverage our combined scale to offer enhanced solutions for our customers.” Oliver has made significant investments in modern equipment, facilities, and people since 2016. The Tap Packaging transaction will represent Oliver’s fifth strategic acquisition and aligns with the company’s vision to build a leading provider of innovative, specialty packaging solutions. The transaction closed on January 18, 2023. To learn more about Oliver, please visit www.oliverinc.com. About Oliver Oliver Inc. is a leading provider of highly customized, quick-turnaround, specialty packaging solutions. Known for its white-glove approach to customer service, the company provides a turnkey platform from design to fulfillment, simplifying complex requirements with consistent on-time, on-budget, ultra-high-quality products and services. About Tap Packaging + Design Since 1906, Tap Packaging + Design has been committed to enhancing their customers’ image by providing high-quality packaging and presentation products. The company’s success can be attributed to the creative craftsmanship of their dedicated workforce, and their sincere desire to partner with their customers and suppliers. Contact Details Oliver Inc. Doug Doroh +1 631-234-1400 ddoroh@oliverinc.com Company Website https://www.oliverinc.com/
January 19, 2023 09:20 AM Eastern Standard Time
News ReleaseAcurx Is Vying for Standard of Care in Treating Primary and Recurrent C. diff
Acurx Pharmaceuticals Inc
By Faith Ashmore, Benzinga C. diff is a life-threatening bacterial infection that causes diarrhea and colitis, which is the inflammation of the colon. Approximately 600,000 are diagnosed with C. diff each year in the United States and it causes approximately 55 deaths a day. In the elderly population, 1 in 11 individuals over the age of 65 die within the month after being infected. The infection has a high recurrent rate, about 1 in 6 patients who get C. diff will get it again within 2-8 weeks. The current treatment for C. diff is vancomycin, an antibiotic that is typically prescribed for serious pathogenic infections. While the drug is safe and has proven successful, the antibiotic has been on the market for 65 years and its effectiveness has been steadily declining as more and more bacteria have become resistant to it, consistent with the path of virtually all other antibiotics over time. Understanding the need for a new antibiotic to treat C. diff, Acurx Pharmaceuticals ( Nasdaq: ACXP ) is developing ibezapolstat, a novel first-in-class antibiotic currently in mid-stage clinical testing. It has been given Fast Track designation by the FDA and has been designated by the FDA as a Qualified Infectious Disease Product (QIDP), which grants priority review by the FDA and provides an additional five years of market exclusivity upon approval. The CDC acknowledges an ”urgent need” for new antibiotics to treat C. diff. During the Phase 2a clinical trial, 100% of the first 10 patients were clinically cured of C. diff and did not have a recurrent infection within a 28-day period after the end of treatment with no safety concerns. Because of these strong results, the Scientific Advisory Board recommended that the trial be stopped early for success. The current standard of care, vancomycin, has an average clinical cure rate of 80% with a 30% chance of recurrent infection. In comparison, ibezapolstat would be a far more suitable drug with a higher success rate if current data holds in late-stage development. Acurx is expecting similarly strong results for their Phase 2b clinical trial. The company is expected to release topline results by mid-2023 if the FDA agrees with the company’s plan for an interim analysis. If the trials continue to be a success and ibezapolstat demonstrates statistical noninferiority compared to vancomycin in curing primary C. diff, it could win FDA approval and be used as first line therapy. But of equal, or even greater, importance are the results being shown in preventing recurrence -- the major cause of C. diff morbidity and mortality, and the principal contributor to C. diff’s $4.5 billion annual cost to the US healthcare system. Being able to reduce or eliminate recurrence would be a game-changing development in treating an infection that affects so many individuals, especially amid rising bacterial resistance to vancomycin. Ibezapolstat’s potential game-changing status would be further assured if it scores well in two exploratory endpoints in the current Phase 2b trial – the number of disease-free patients at days 60 and 90 (two time points not included on any product labeled for C. diff.) and if it continues to demonstrate restoration of the healthy microbiome of C. diff patients during the treatment process. Click here for more information about Acurx. About Acurx Pharmaceuticals, Inc. Acurx Pharmaceuticals is a clinical stage biopharmaceutical company focused on developing an entirely new class of antibiotics for difficult to treat infections. The Company's approach is to develop antibiotic candidates that target the DNA polymerase IIIC enzyme and its R&D pipeline includes antibiotic product candidates that target Gram-positive bacteria, including Clostridioides difficile, methicillin-resistant Staphylococcus aureus (MRSA), vancomycin resistant Enterococcus (VRE) and drug-resistant Streptococcus pneumoniae (DRSP). To learn more about Acurx Pharmaceuticals and its product pipeline, please visit www.acurxpharma.com This post contains sponsored advertising content. This content is for informational purposes only and is not intended to be investing advice. Photo by Mark Fletcher-Brown on Unsplash Contact Details Acurx Pharmaceuticals, Inc. David P. Luci, President & CEO +1 917-533-1469 davidluci@acurxpharma.com Company Website https://www.acurxpharma.com/
January 19, 2023 09:00 AM Eastern Standard Time
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News ReleaseVistagen Poised To Begin Phase 1 Trial Of A Fast-Acting Antidepressant Nasal Spray In First Quarter Of 2023
VistaGen
By Rachael Green, Benzinga In the race to create faster-acting, safer antidepressants, Vistagen (NASDAQ: VTGN) is starting the year strong as it gets ready to launch a Phase 1 Trial of its novel pherine nasal spray for Major Depressive Disorder (MDD). The trial, involving the Company’s newly optimized formulation of PH10, is intended to confirm the favorable safety profile of PH10 established in three previous clinical studies conducted in Mexico, including a published Phase 2A study for the treatment of MDD. After receiving a “study may proceed” letter from the U.S. Food and Drug Administration (FDA) last November followed by a Fast-Track designation from the FDA in December, the late clinical-stage biopharmaceutical company is ready to start the Phase 1 trial in the first quarter of 2023. Upcoming Phase 1 Clinical Trial Will Prepare Vistagen’s Drug Candidate PH10 for Phase 2B Research On November 30, Vistagen announced that it had received a “study may proceed” letter from the FDA for PH10 as a treatment for MDD. The following week, the FDA granted Fast-Track designation to the pherine-based nasal spray. The FDA’s fast track program, meant to bring promising new treatments for serious conditions to patients sooner, makes Vistagen’s drug eligible for more frequent meetings and communications with the FDA – which can help ensure a smoother development and review process and, potentially, an earlier drug approval date. The FDA’s decision to grant Fast-Track designation was based on Vistagen’s previous preclinical and clinical research on PH10. In an earlier Phase 2A study of PH10, for example, the MDD treatment was found to significantly reduce depressive symptoms in participants after only one week of treatment and at the eight-week study endpoint. The upcoming Phase 1 study will enroll 12 participants in a double-blind, placebo-controlled clinical trial with topline data expected by the end of the first quarter. The goal of the study is to confirm the favorable safety data demonstrated in earlier clinical trials and lay the groundwork for a Phase 2B study of PH10 in MDD. On December 21, Vistagen announced its acquisition of Pherin Pharmaceuticals, a clinical-stage company developing a pipeline of pherine drug candidates. The acquisition will give Vistagen full ownership of the intellectual property rights for both PH10 and its Phase 3 pherine drug candidate, PH94B, allowing the company to stop paying royalties and milestone payments for the compounds. The deal will also add three new pherine drug candidates to Vistagen’s pipeline. PH10 Is Designed To Be A Fast-Acting Antidepressant With Minimal Side Effects In the past few years, research activity in the MDD space has picked up significantly as companies explore several new treatment options with different mechanisms of action. That’s because the currently approved antidepressants aren’t working for millions of people, leaving a massive unmet need that drug developers are racing to fill. “Nearly two-thirds of diagnosed and treated depression patients do not achieve remission with first-line therapy. With 21 million adults in the U.S. suffering at least one major depressive episode in the past year, potentially millions of individuals are not getting the help they need,” said Vistagen CEO Shawn Singh in a statement about the upcoming Phase 1 trial for the MDD treatment. While some exciting progress has been made, Vistagen hopes its drug candidate, PH10, can address some of the shortcomings of the latest alternatives to hit the market. PH10 is one of two pherine nasal sprays currently in development at Vistagen. Pherines are a new class of synthetic chemosensory messenger drug candidates that may be able to provide fast-acting relief for depression and anxiety symptoms and several other unmet medical needs. For the treatment of depression, PH10 is designed to activate chemosensory neurons in the nose that can then activate the limbic system, the areas of the brain involved in emotional response. Researchers hypothesize that it does this possibly by triggering the release of more dopamine, serotonin, and norepinephrine, three hormones that play a role in mood and happiness. This mechanism of action sets it apart from other drugs in development for depression. COMPASS Pathways, PLC (NASDAQ: CMPS), for example, is working on COMP 360 – a psilocybin-based therapy for treatment-resistant depression – which has shown promise in recent clinical trials. In one Phase 2b study, a single high dose of the psilocybin compound was able to provide immediate symptom improvement with results lasting up to 12 weeks. However, being a psychedelic, the treatment requires psychological support from a specialty-trained therapist during a psilocybin therapy session. While it may be helpful in the long run, the time-consuming process isn’t as convenient as a standalone medication that could be taken daily or as needed without interrupting the rest of the day. Meanwhile, Relmada Therapeutics, Inc. (NASDAQ: RLMD) is developing REL-1017, a compound that works by blocking the N-Methyl-D-aspartate (NMDA) receptor in the brain. The daily oral treatment is meant to work similarly to ketamine-derived treatments like Johnson & Johnson’s (NYSE: JNJ) recently approved Spravato, but without the psychotropic effects. However, the late-stage biotech announced top-line results from its Phase 3 trial of the drug candidate last October, noting that it failed to achieve its primary endpoint of significantly reducing depression symptoms compared to a placebo. PH10, on the other hand, does not require the same systemic uptake to produce its fast-acting effects, according to Vistagen. The compound doesn’t cause the same psychotropic side effects as ketamine-based treatments but has still managed to demonstrate rapid-onset and significant lasting results in the clinical studies completed so far. As trials progress, it could be worth keeping on the company as it leverages its recent wins to bring its drug to market quickly for the millions suffering from depression. This article was originally published on Benzinga here. Vistagen (Nasdaq: VTGN) is a late clinical-stage biopharmaceutical company aiming to transform the treatment landscape for individuals living with anxiety, depression and other CNS disorders. The Company is advancing therapeutics with the potential to be faster-acting, and with fewer side effects and safety concerns, than those that are currently available. Vistagen’s clinical-stage candidates are targeting multiple forms of anxiety and depression. PH94B and PH10 belong to a new class of drugs known as pherines, which are investigational neuroactive steroid nasal sprays designed with a novel rapid-onset mechanism of action that activates chemosensory neurons in the nasal passages and can impact the olfactory-amygdala neural circuits without systemic uptake or direct activity on CNS neurons in the brain. Vistagen is passionate about transforming mental health care and redefining what is possible in the treatment of anxiety and depression. This post contains sponsored advertising content. This content is for informational purposes only and not intended to be investing advice. Contact Details Mark Flather- Investor Relations mflather@vistagen.com Company Website https://www.vistagen.com/
January 19, 2023 08:30 AM Eastern Standard Time
News ReleaseAmeriLife Announces Key Organizational Changes on Heels of Strong Growth & Expansion
AmeriLife
Following three years of record-breaking growth and expansion, AmeriLife Group, LLC (“AmeriLife”) today announced a strategic, organizational restructuring with the creation of two new, distinct distribution groups – Wealth and Health – an evolved structure designed to deliver more focused growth along with the resources needed to continue to grow AmeriLife’s industry-leading partners. Wealth will be led by AmeriLife’s Chief Distribution Officer Mike Vietri, reporting to AmeriLife Chairman and CEO Scott R. Perry. Health will be led by newly appointed Chief Distribution Officer and former president of AmeriLife’s Life & Health Brokerage Distribution Scotty Elliott, reporting to AmeriLife’s Chief Operating Officer Tim Calvert. “This reorganization represents a natural evolution of our strategy. Five years ago, AmeriLife embarked on a journey to build the capabilities that we would need to deliver on our mission of offering a full suite of insurance and retirement solutions to provide people peace of mind, enabling them to live longer, healthier lives,” said Perry. “Through execution of our organic and inorganic growth plans, we are now at a stage where we’ve assembled comprehensive capabilities across the spectrum of Health and Wealth to deliver a platform of products and technology that agents and advisors can utilize to effectively deliver holistic solutions to the market, engaging with consumers through their channels of choice. “We are fortunate to have a talented and experienced group of senior leaders at the helm of this new structure to optimize this platform. Additionally, the new structure provides a laser focus on our two core areas of business, affording even greater growth and profitability opportunities within Wealth and Health.” Wealth Distribution Over the past seven years, Vietri has grown AmeriLife’s distribution organization to over $9 billion in overall premium, $7.2 billion in assets under management, and more than 120 affiliates and agencies nationwide. Given his depth of knowledge and experience in the wealth management and financial services industries, and considering the growing demands of the organization, Vietri’s focus, going forward, will be on AmeriLife’s annuities, underwritten life, and wealth and retirement advisory verticals. Saybrus, TruChoice Financial Group, ICON and Brookstone will remain key to AmeriLife’s overall Wealth strategy. Vietri will continue to report to Perry, while AmeriLife Benefits and AmeriLife’s Career Agency will continue to report to Vietri under their current leadership. Additionally, AmeriLife’s Distribution Centers of Excellence, including Distribution Analytics, Distribution Operations, and its Business Revenue Group (BRG), will continue to report to Vietri and maintain their enterprise focus. AmeriLife’s Wealth-focused affiliates will continue to report to Denny Southern. “Over the last few years, AmeriLife’s efforts to add to its wealth-focused services and solutions has set us up for continued growth in the space at exactly the right time,” said Vietri. “I’m incredibly excited for the realignment of our organization. In particular, I’m thrilled to lead AmeriLife’s Wealth Distribution at time when our offerings align perfectly with consumers’ needs and our holistic approach to wealth management and retirement planning ensures customers never outgrow our advisors.” Health Distribution Elliott joined AmeriLife in 2019 with a focus on distribution business development, and was elevated soon thereafter to lead AmeriLife’s Life & Health Brokerage Distribution, overseeing field distribution initiatives, carrier partnerships, and IMO and FMO relationships. Reporting to Calvert, Elliott will take on AmeriLife largest and fastest-growing business. Their stewardship of Health will allow AmeriLife to deliver even greater strategic efficiencies – at scale – to ensure sustainable growth for its partners. In his new role, Elliott will continue lead AmeriLife’s Medicare and Simplified Issue Life verticals, as well as assume accountability of AmeriLife’s Direct-to-Consumer distribution arm, which will continue to be led by Jim Palmer. “I’m humbled by the opportunity to lead AmeriLife’s Health Distribution,” said Elliott. “I’m forever indebted to Scott and Mike for their support and leadership, and hope to make them proud with this new venture. I also want to commend the talented group of affiliates that comprise AmeriLife. They are the reason we are experiencing so much success, and I’m eager to serve them for years to come.” Since 2020, AmeriLife has added 65 affiliates serving more than 350,000 agents and advisors nationwide. While its Life & Health business has more than doubled in size during the same time period, the company remains equally focused on growth opportunities and synergies within its wealth-focused lines of businesses, strengthened by the recent addition of TruChoice Financial Group, its joint venture ICON with AIMCOR Group, and evidenced by more than $8 billion in annuities premiums and more than $7 billion in assets under management as of the end of 2022. Added Perry: “I couldn’t be happier for Mike and Scotty as they assume their new leadership roles and pursue more ways to serve and support our trusted and talented affiliate partners, which will allow them to achieve new levels of growth and success.” ### About AmeriLife AmeriLife’s strength is its mission: to provide insurance and retirement solutions to help people live longer, healthier lives. In doing so, AmeriLife has become recognized as the leader in developing, marketing, and distributing life and health insurance, annuities and retirement planning solutions to enhance the lives of pre-retirees and retirees across the United States. For more than 50 years, AmeriLife has partnered with top insurance carriers to provide value and quality to customers served through a distribution network of over 350,000 insurance agents and advisors and more than 100 marketing organizations and insurance agency locations nationwide. For more information, visit AmeriLife.com, and follow AmeriLife on Facebook and LinkedIn. Contact Details Media Jeff Maldonado +1 321-297-1112 jmaldonado@amerilife.com Partnership Inquiries Patrick Nichols +1 727-726-0726 pnichols@amerilife.com Company Website https://amerilife.com/
January 18, 2023 02:50 PM Eastern Standard Time
