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Aira Health Unveils Innovative Wellness Solutions for Women's Health

Aira Health Unveils Innovative Wellness Solutions for Women's Health

Schuylerville, NY, Aug. 15, 2025 (GLOBE NEWSWIRE) -- Aira Health, a women's wellness brand dedicated to reducing overwhelm in the health space, proudly announces the launch of its first line of science-backed supplements formulated to support hormone balance, gut health, immune regulation, metabolism, and autoimmune recovery.
Melissa Rose, AFMP, CHHC, AADP
Created by Melissa Rose, AFMP, CHHC, AADP, an internationally recognized functional medicine practitioner known for her work with complex and rare autoimmune conditions, Aira Health's new formulations offer a grounded, gentle approach to everyday wellness challenges.
'These products were born out of real need,' said Melissa Rose. 'After years of working with women struggling with fatigue, bloating, brain fog, hormone swings, and autoimmune flares, I wanted to create a simpler path. These formulas reflect what's worked in clinical practice - rooted in nature, backed by science, and gentle enough for daily use.'
The launch includes four targeted supplements:
Each product is intentionally crafted to work together or stand alone—providing a safe, synergistic foundation for women navigating hormonal transitions, autoimmune conditions, or chronic symptoms.
With a focus on clarity over confusion, Aira Health is committed to demystifying women's wellness. The formulas are free of synthetic hormones and unnecessary additives, and each ingredient was selected to gently support root systems of health without pushing or overriding the body.
This launch marks the first phase of Aira's broader vision: to create a calm, empowered space for women to reconnect with their bodies and receive the support they need, without the overwhelm. Later this year, Aira will debut My Aira Circle, a membership community offering symptom relief strategies, guided protocols, breathwork sessions, and expert Q&As.
Aira Health is more than supplements, it's a movement toward simple, sustainable wellness that helps women feel like themselves again.
To learn more or request samples, please visit www.myairahealth.com or contact [email protected].
Aira Health - a new era of wellness for women.
About Aira Health
AIRA is a women's wellness brand offering targeted supplements to support hormone balance, gut health, immune regulation, metabolism, and autoimmune recovery. Created by Melissa Rose, AFMP, CHHC, AADP—an internationally recognized functional medicine practitioner known for her work in complex and rare autoimmune conditions—AIRA blends science-backed formulas with a deep understanding of what it really takes to feel better.
Press inquiries
Aira Health
https://myairahealth.com/
Melissa Rose, AFMP, CHHC, AADP
[email protected]
PO Box 151, Schuylerville, NY 12871
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Pfizer battles another Paxlovid lawsuit from Enanta
Pfizer battles another Paxlovid lawsuit from Enanta

Yahoo

time27 minutes ago

  • Yahoo

Pfizer battles another Paxlovid lawsuit from Enanta

If you don't succeed at first, try again – in separate regions. That's the motto Enanta Pharmaceuticals is following, at least, after disclosing it has sued Pfizer in Europe over a patent infringement relating to Covid-19 treatment pill Paxlovid (nirmatrelvir/ritonavir). In June 2022, Enanta filed a lawsuit against Pfizer in a US district court in Massachusetts, claiming that the big pharma company infringed on a patent describing protease inhibitors invented by its scientists. Enanta has now followed that up with another filing in Europe, making the same accusation. Since being emergency authorised in 2021, anti-viral Paxlovid has generated Pfizer more than $26bn in global revenue. This includes a staggering $18.9bn in 2022 when Covid-19 cases were still prevalent. Despite waning demand for Covid-19 treatments, the pill still brought in $1.2bn in 2024, buoyed by government orders. However, Enanta – known for co-developing hepatitis C virus treatment glecaprevir/pibrentasvir with AbbVie – believes Pfizer designed Paxlovid via unlawful means. The US biotech stated it is 'seeking a determination of liability for use and infringement of European Patent No. EP 4 051 265 (the '265 Patent) in the manufacture, use and sale of Pfizer's Covid-19 antiviral, Paxlovid'. In an emailed statement to Pharmaceutical Technology, a Pfizer spokesperson said: 'We are confident in our intellectual property (IP) surrounding Paxlovid and will respond in due course in court.' The lawsuit, filed in the European Union's (EU) Unified Patent Court (UPC), targets Pfizer's commercial activity in the 18 countries of the EU. The company confirmed the '265 patent in question is the European counterpart of US patent number 11,358,953 (the '953 Patent) that is the centre of the US lawsuit. Although it is technically ongoing, Enanta's US lawsuit hit a major roadblock. In December 2024, a federal judge in Massachusetts sided with Pfizer, granting that the '953 patent is invalid. Enanta confirmed at the time it would appeal the decision, adding it 'believes strongly in the merits of our case'. Pfizer reported strong Q2 2025 results this month, bucking a tepid earnings window that gripped the wider pharma industry. Sales for the Paxlovid grew 71% while the Covid-19 vaccine Comirnaty revenue surged 95%. However, the legal challenge posed by Enanta marks the second issue Pfizer has had to firefight this week. The big pharma company reported a Phase III trial failure for a sickle cell disease candidate purchased as part of a $5.4bn takeover of Global Blood Therapeutics in 2022. "Pfizer battles another Paxlovid lawsuit from Enanta" was originally created and published by Pharmaceutical Technology, a GlobalData owned brand. The information on this site has been included in good faith for general informational purposes only. It is not intended to amount to advice on which you should rely, and we give no representation, warranty or guarantee, whether express or implied as to its accuracy or completeness. You must obtain professional or specialist advice before taking, or refraining from, any action on the basis of the content on our site. Sign in to access your portfolio

Human Osteoblasts Market to Reach US$ 87.1 Million by 2033
Human Osteoblasts Market to Reach US$ 87.1 Million by 2033

Yahoo

time27 minutes ago

  • Yahoo

Human Osteoblasts Market to Reach US$ 87.1 Million by 2033

The market is currently experiencing robust growth, fueled by a post-pandemic surge in orthopedic surgeries and significant investment in regenerative medicine. Innovations in 3D bioprinting and smart scaffolds are creating new therapeutic possibilities for bone repair. Chicago, Aug. 20, 2025 (GLOBE NEWSWIRE) -- The global human osteoblasts market was valued at US$ 48.2 million in 2024 and is expected to reach US$ 87.1 million by 2033 at a CAGR of 6.8% during the forecast period 2025–2033. The future potential of the human osteoblasts market lies in the convergence of artificial intelligence with advanced biomanufacturing. AI-powered platforms are now capable of analyzing genomic data from 1000s of individuals to predict osteoblast response to new drug compounds, drastically reducing discovery timelines. This synergy is enabling the creation of patient-specific 3D-bioprinted bone grafts. As of 2025, researchers are successfully embedding patient-derived osteoblasts into custom scaffolds with 95% cell viability post-printing. These constructs are being tested in preclinical models for craniofacial reconstruction and spinal fusion, promising a new era of personalized regenerative medicine. Demand for highly characterized osteoblasts for these applications is projected to soar. Download Sample Pages: Another significant growth frontier of the human osteoblasts market is the application of osteoblast research to counteract microgravity-induced bone loss in astronauts. With 3 new long-duration space missions planned by international agencies before 2028, research into osteoblast function in simulated microgravity is intensifying. Furthermore, the veterinary orthopedics market represents a substantial, untapped opportunity. In 2024, an estimated 1.2 million companion animals in the U.S. alone underwent procedures for fractures or degenerative joint diseases. 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Top 12 Key Players Strategically Dominate the Evolving Global Human Osteoblasts Market The competitive environment is both concentrated and highly specialized. Analysis in 2024 consistently identifies 12 key players shaping the industry. These include Sigma-Aldrich, Athersys Inc., Cerapedics Inc., CryoLife, Inc., and Cytori Therapeutics Inc. Other notable companies are USA Stem Cell Inc., Vericel Corporation, Wright Medical Group N.V, Biocomposites, BD, Zimmer Biomet, and PromoCell. In the crucial U.S. orthopedic biomaterials sector, a key application area, 3 major competitors—Medtronic, DePuy Synthes, and Stryker—were noted as dominant forces in 2024. Suppliers offer highly specific product lines to meet diverse research needs. As of 2025, PromoCell provides 4 primary product categories related to osteoblasts, including cells and specialized growth media. 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Quality Guarantees and Emerging Technologies Redefine the Global Human Osteoblasts Market The reliability of research outcomes depends on the quality of the underlying cell products. Suppliers in the market provide stringent quality guarantees. PromoCell guarantees >500,000 viable cells per cryovial after thawing. Innoprot similarly ensures >500,000 viable cells in each vial, cryopreserved at passage one, while Lonza guarantees ≥500,000 viable cells per ampule. For immortalized lines, Innoprot provides >1,000,000 viable cells per vial, and InSCREENex includes >0.5 million viable cells per vial. Longevity in culture is also specified. Innoprot guarantees 15 population doublings for its primary osteoblasts post-delivery. PromoCell recommends a split ratio of 1:3 to 1:6 for its primary cells. To support targeted research, PromoCell holds >100 HLA-typed cell donors in stock as of 2024, offering 4-digit high-resolution typing. The InSCREENex cell line was derived from a 63-year-old female donor. Concurrently, emerging technologies are creating new opportunities for the human osteoblasts market. Three key trends noted in the 2024 orthopedic biomaterials market are biodegradable materials, 3D printing, and nanotechnology. A September 2024 paper detailed 1 study using collagen-based 3D printed scaffolds to investigate osteoblast activity. A May 2024 publication described 1 new 3D in-vitro model using human fetal osteoblasts. A 2025 study utilized 2 cell lines to test 3D printed composite samples, using standards prepared from 1,000 mg/L stock solutions and a plating density of 10,000 cells/well for viability tests. Customize the Data Scope to Match Your Objectives: Strategic Alliances and Focused Regional Developments Indicate Strong Global Market Growth Corporate strategies and regional activities in 2024 and 2025 underscore a commitment to global expansion of the human osteoblasts market. On March 10, 2024, 1 major collaboration was announced between Athersys Inc. and Cerapedics Inc. to develop a novel osteoblast-based therapy. Service providers are also expanding. In 2024, Thermo Fisher launched its "Accelerator™ Drug Development" solutions, offering 360-degree support to biotech companies. Licensing agreements are expanding market access for key biologics. Bio-Thera Solutions entered into 1 exclusive licensing agreement on December 24, 2024, for its ustekinumab biosimilar. On the same day, GlycoNex announced 1 licensing agreement for its denosumab biosimilar, a therapy for bone loss. Regional market activities are intensifying. In 2024, 1 pivotal Phase 2 trial for osteosarcoma was opened in Barcelona, Spain. Stryker expanded with 1 new testing facility in India in February 2024. In May 2024, Sanofi announced 1 new partnership with OpenAI to accelerate R&D. The North American market saw the FDA grant 1 US approval to Pfizer's Beqvez on April 25, 2024. Europe showed activity with 1 approval by the UK's MHRA on January 15, 2025. The Asia-Pacific region is also growing, evidenced by 1 approval in Japan on January 7, 2025, for Biocon's ustekinumab. Global Human Osteoblasts Market Major Players: Athelas Bionova Scientific Cell Signaling Technology Corning EMD Millipore Invitrogen Lonza Merck Group NantKwest Promega R and D Systems ReproCELL Sigma-Aldrich Stemcell Technologies Thermo Fisher Scientific Other Prominent Players Key Market Segmentation: By Product Human Cell Culture Osteoblast Cell Lines By Application Traumatic Injuries Road Accidents Regeneration Surgeries Orthopedics Musculoskeletal and Spine Neurology By End user Hospitals Specialty Clinics Ambulatory Surgical Centers By Region North America Europe Asia Pacific Middle East & Africa South America Need a Detailed Walkthrough of the Report? Request a Live Session: About Astute Analytica Astute Analytica is a global market research and advisory firm providing data-driven insights across industries such as technology, healthcare, chemicals, semiconductors, FMCG, and more. We publish multiple reports daily, equipping businesses with the intelligence they need to navigate market trends, emerging opportunities, competitive landscapes, and technological advancements. With a team of experienced business analysts, economists, and industry experts, we deliver accurate, in-depth, and actionable research tailored to meet the strategic needs of our clients. At Astute Analytica, our clients come first, and we are committed to delivering cost-effective, high-value research solutions that drive success in an evolving marketplace. Contact Us:Astute AnalyticaPhone: +1-888 429 6757 (US Toll Free); +91-0120- 4483891 (Rest of the World)For Sales Enquiries: sales@ Follow us on: LinkedIn | Twitter | YouTube CONTACT: Contact Us: Astute Analytica Phone: +1-888 429 6757 (US Toll Free); +91-0120- 4483891 (Rest of the World) For Sales Enquiries: sales@ Website: in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Valley Fever Cases Surge To Record Levels In California
Valley Fever Cases Surge To Record Levels In California

Forbes

time28 minutes ago

  • Forbes

Valley Fever Cases Surge To Record Levels In California

California is experiencing an unprecedented surge in Valley Fever cases, with health officials warning that 2025 could shatter previous records. As of the end of July, there were 6,761 confirmed cases, which means if this pace continues, the total 2025 numbers will likely exceed the 12,595 cases reported in 2024. This dramatic increase has prompted renewed public health warnings and highlights the urgent need for greater awareness of this potentially serious fungal infection. What Causes Valley Fever and How Is It Transmitted? Coccidioidomycosis, commonly known as Valley Fever, is caused by the fungus Coccidioides, which exists naturally in the soil of certain arid and semi-arid regions. The fungus thrives in areas with hot, dry summers and mild winters, making California, Arizona, and parts of Nevada, New Mexico, and northern Mexico prime endemic zones. The disease is transmitted through inhalation of fungal spores called arthroconidia. When soil containing the fungus is disturbed by activities such as construction, farming, excavation, or strong winds, the microscopic spores become airborne and can travel significant distances. People become infected by breathing in dust particles that are contaminated with the microscopic spores. Importantly, Valley Fever is not contagious between people or animals, meaning that an infected person can't transmit the disease to another individual or pet. The infection comes exclusively from environmental exposure to contaminated soil. Weather patterns and climate change have significantly impacted the risk of transmission. Periods of increased rainfall followed by dry conditions create an ideal setting for fungal growth and subsequent dispersion of the spores. This explains why California has seen such a dramatic increase in cases following recent wet winters, as the enhanced fungal growth eventually leads to greater spore production when conditions dry out. Often Silent, Yet Potentially Deadly Fortunately, nearly 60% of those who are infected with Coccidioides will not develop symptoms. However, in the remaining 40%, symptoms typically appear one to three weeks after exposure, though they can emerge anywhere from a few days to several months later. The disease presents in various forms, ranging from mild to severe. Most people with Valley Fever experience flu-like symptoms that can persist for weeks to months. Symptoms can include persistent fatigue, fever, dry cough, chest pain, shortness of breath, headaches, muscle aches, and joint pain. Many patients also develop a characteristic skin rash with red bumps or patches. The fatigue associated with Valley Fever can be particularly debilitating and may last for months even after other symptoms resolve. In approximately 5-10% of cases, the infection may progress to a chronic pulmonary form, causing persistent pneumonia-like symptoms, with the development of lung nodules that may be seen on chest X-ray. Less commonly, the infection can spread beyond the lungs to other parts of the body, including bones, joints, skin, and the central nervous system. This disseminated form is more serious and has a higher prevalence in pregnant women, people with a compromised immune system, and certain ethnic groups including African Americans, Filipinos, and Hispanics. Testing and Diagnosis Diagnosing Valley Fever can be challenging because its symptoms may closely resemble other respiratory illnesses. Many cases go undiagnosed or are misdiagnosed, leading to unnecessary antibiotic treatment and delayed prescription of antifungal medication. Several testing methods are available for diagnosis. Blood (i.e., serology) tests can detect antibodies that the immune system produces in response to the fungal infection. The fungus can also be grown in culture, but this can take several days, which may delay diagnosis and treatment. Molecular, or PCR, tests are available at select laboratories and can provide a rapid diagnosis from samples such as sputum, tissue or cerebrospinal fluid. Healthcare providers should consider Valley Fever testing for patients in endemic areas who present with persistent respiratory symptoms, especially during peak transmission seasons, which are usually late fall and early winter. Prevention Strategies While it's impossible to completely eliminate the risk of Valley Fever in endemic areas, several measures can significantly reduce the risk of becoming infected. The most effective prevention involves minimizing exposure to dust and disturbed soil. During high-risk periods, particularly windy days or dust storms, people should stay indoors with windows and doors closed and use air purification systems with high-efficiency filters. When outdoor activities are necessary, wearing a mask can provide protection against inhaling fungal spores. Those working in high-risk occupations, such as construction or agriculture, should use appropriate respiratory protection. Individuals at higher risk for severe disease, including pregnant women or those with a compromised immune system, should take extra precautions. This may include avoiding high-risk activities entirely and consulting with their healthcare provider about steps to stay safe and symptoms to watch out for. As Valley Fever cases continue to climb in California and other southwestern states, awareness and prevention become increasingly important. Understanding this fungal disease, recognizing its symptoms, and taking appropriate protective measures can help individuals and communities better navigate this growing public health challenge.

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