Gemeinsamer Bundesausschuss (G-BA) Proposes Inclusion of Tapentadol in Fixed Price Group: Public Consultation Outcomes The Gemeinsamer Bundesausschuss (G-BA), Germany's top healthcare decision-making body, has proposed an amendment to the Drug Directive to include Tapentadol in the fixed price group system. This aims to ensure cost-efficiency in the public healthcare system. After extensive public consultation, which involved stakeholders like Grünenthal Group, a producer of Tapentadol, the Gemeinsamer Bundesausschuss (G-BA) decided that Tapentadol meets the criteria for inclusion. Despite concerns about European production costs and rebate contracts, the Gemeinsamer Bundesausschuss (G-BA) emphasized that the fixed price group would ensure affordable access to Tapentadol while maintaining therapeutic effectiveness, with implementation set for September 2024. For more details please click the link! https://lnkd.in/dhrhH2DS #marketaccess #reimbursement #pricing #hta #heor #healtheconomics #medicaldevices #pharmaceutical
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How to keep GPs informed out about new medications? With the TGA approving many new prescription medicines in 2024, pharma companies have the challenge as to how best update doctors on all these changes so that they can prescribe the most effective treatments based on the latest drug advancements. adg's Inside Healthcare looks back through the archives to share learning’s on this highly relevant topic. #PharmaGTM #PharmaMarketing
How do busy GPs want to find out about new medications? | Australian Doctor Group
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Choosing the right partner makes all the difference.
#Prescriptiondrugcosts are increasingly posing barriers to to care for many Americans, especially given ongoing #drugflation, particularly for specialty medications. However, #Humira, one of the biggest market drivers for more than the last decade recently lost patent protection and more high-cost drugs are about to, raising the possibility that #biosimilars can help bring about a sea change to the pharmaceutical landscape. #RxBenefits
Biosimilars continue to drive market competition and increase savings for seniors
phrma.org
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This strategic partnership between Community Health Systems and Cost Plus Drugs represents an innovative approach to addressing rising pharmaceutical costs and drug shortages. This collaboration feels like a real game-changer for making crucial medications more affordable and accessible for patients. This partnership also represents a promising step towards addressing major issues impacting healthcare affordability and accessibility. Innovative collaborations like this have the potential to positively transform the pharmaceutical supply chain for both healthcare providers and patients.
Community Health Systems Partners With Mark Cuban Cost Plus Drug Company to Address the Rising Cost of Drugs and Potential Drug Shortages
businesswire.com
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🚨 Breaking News: G-BA Ends Data Collection Requirement for Marstacimab! 🚨 In a significant move, Berlin's Federal Joint Committee (G-BA) has officially halted the mandate for application-related data collection on Marstacimab, following its approval as an orphan drug. This decision underscores the stringent criteria surrounding data collection mandates and highlights how orphan drug classification can streamline regulatory processes. Key Highlights: ✅ Marstacimab approved for routine prophylaxis in patients aged 12+ with severe hemophilia A or B. ✅ G-BA's decision reflects a broader trend in pharmaceutical strategies to optimize market access. ✅ Patients can now expect quicker access to essential treatments, enhancing health outcomes. This development not only benefits pharmaceutical companies but also paves the way for improved patient care. For more insights on this pivotal decision and its implications, click on the link! #G-BA #HealthcareInnovation #Marstacimab #OrphanDrug #Pharma #PharmaceuticalNews #RegulatoryAgencies #RegulatoryUpdates #MarketAccess #MarketAccessToday
G-BA Ends Data Collection Requirement for Marstacimab
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The next round of #InflationReductionAct Medicare Drug Price Negotiations is coming soon, with the next 15 #drug brands to be announced by Feb. 1st. As the piece below states, the selection process is rigorous. What they don't say is that the process that the selected companies have to go through is also quite rigorous. It is a process like no other, that requires fine-tuned coordination of a cross-functional team, and a clear roadmap for each step of the way. If you are one of those companies, are you ready? https://lnkd.in/eXpd3QG9 #IRA #Medicare #DrugPriceNegotiation
💊 Medicare's Prescription Drug Price Negotiations: A Game Changer Ahead! 💊 As the healthcare landscape evolves, the spotlight is on Medicare's upcoming negotiations for 15 brand-name drugs in 2025. This pivotal moment could reshape market access and affordability for patients relying on these essential medications. 🔍 Key Insights: - The selection process is rigorous, focusing on patient health impact, Medicare costs, and market exclusivity. - Potential price reductions may enhance accessibility but challenge pharmaceutical companies to rethink their pricing strategies. - The outcomes could set new precedents for future pricing policies and market dynamics. Stay informed about how these negotiations will influence both patients and the pharmaceutical industry! 👉 Click to read more about what to expect in this critical development! #DrugPricing #HealthEconomics #Healthcare #MarketAccess #Medicare #Pharmaceuticals #Publications #MarketAccess #MarketAccessToday
Medicare’s Upcoming Prescription Drug Price Negotiations: What to Expect
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Prescription medication costs are on the rise, disproportionately affecting communities of color. Recent findings from Patients For Affordable Drugs, reveals that Black and Latino seniors struggle more to afford their medicine, while pharmaceutical companies continuously increase prices for drugs like Enhertu and Revlimid. No one should have to make the difficult choice between essential medications and basic needs. It's time for policy action to counter the greed of Big Pharma and promote health equity. https://lnkd.in/gRjrEV85 #AffordablePrescriptions #AffordableDrugsNow #BigPharma #EndBigPharmaGreed #HealthEquity #OCAP
New prescription drug price hikes hit Black patients hard
nbcnews.com
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An interesting read about the recent Senate H.E.L.P. Committee hearing on prescription drugs costs. Pharmaceuticals represent only ~14% of US healthcare spend, but often take on an inordinate share of blame for the problem of healthcare affordability and suboptimal outcomes in the US. The problems of the US healthcare system are multifactorial- rooted in the fee-for-service model and the complex web of healthcare delivery, payers, PBMs, pharmaceutical and medical device companies. The author asserts that changes in one part of the healthcare ecosystem will have significant impacts on other components, the total cost of care, and overall health outcomes, so there is no easy solution. https://lnkd.in/ezZwBb3J
Bernie Sanders Wants To Rein In Drug Prices. Is He Asking The Right Questions?
forbes.com
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PBMs in the Pharmaceutical Industry are under scrutiny for perceived lack of transparency, misaligned incentives, and failure to demonstrate value. The intricate roles of key players hold stakes in the game. Discover how to achieve full accountability. #PharmaceuticalIndustry #Healthcare #HealthcareInnovation
White Paper - The Highly Complex Pharmacy Supply Chain
risk-strategies.com
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Medicine Just Got a Digital Upgrade with Software-Enhanced Drugs™. Yesterday, at The Frontiers Health conference, Click Founder and CEO David Benshoof Klein delivered his keynote, speaking to a future where software-enhanced drug™ therapies will be standard of care. Software-enhanced drug therapies are drug-software combination products that target the unique needs of a medication and patient population to deliver added clinically meaningful benefit. The value of these therapies is reinforced by FDA's Prescription Drug Use Related Software (PDURS) Draft Guidance, which outlines how the FDA intends to apply its drug labeling authorities to software outputs associated with prescription drugs. The guidance covers a full spectrum of use cases, but importantly specifies that when software used with a drug demonstrates added clinically meaningful benefit compared to drug alone in one or more adequate and well-controlled trials, that added clinical benefit can be included in the drug label, right in the package insert. These will soon be routinely developed and launched for leading pharmaceutical brands as “SE” (software-enhanced) dosage forms, e.g., “*Drug Name*™ SE™”. Software-enhanced drug products are thus a high-value, high-rigor category of product within PDURS. Compared to other PDURS solutions, these treatments are differentiated by a high level of clinical validation, development in compliance with software-as-a-medical device requirements for cybersecurity and quality, and offer patients an engaging and personalized treatment experience to achieve superior clinical outcomes. To learn more, visit us next week at HLTH (Booth #2137) or reach out to bd@clicktherapeutics.com #FrontiersHealth #FH24 #FrontiersHealth24 #PDURS #PrescriptionDigitalTherapeutics #DrugDevelopment #SoftwareEnhancedDrugs
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Check out last week's top stories from Market Access Today! #marketaccess #reimbursement #pricing
We have compiled the week's top news for you at Market Access Today! - In a groundbreaking analysis conducted by ECONiX Research, a detailed examination of the Turkish Pharmaceutical and Medical Device Agency’s (TİTCK - Türkiye İlaç ve Tıbbi Cihaz Kurumu) Detailed Drug List has shed light on the escalating costs of pharmaceuticals in Turkiye’s pharmaceutical market. (https://lnkd.in/dhZiQKGk) - The latest edition of the Schönermark Kielhorn Collegen’s (SKC Beratungsgesellschaft mbH) InnovATion NavigATor for Advanced Therapy Medicinal Products (ATMPs), offers an in-depth analysis that sheds light on the significant progress and challenges in the field of Advanced Therapy Medicinal Products, especially in their journey through the AMNOG process. (https://lnkd.in/dq-TkV-5) - The NICE - National Institute for Health and Care Excellence is pioneering a novel approach to stroke treatment with its latest proposal for genetic testing. By leveraging advances in genetic research, this groundbreaking strategy seeks to enhance the precision of post-stroke care, ensuring that patients receive the most effective stroke treatment based on their unique genetic makeup. (https://lnkd.in/dm3RbpWp) - The U.S. Food and Drug Administration (FDA) has approved Rejoyn, marking a groundbreaking achievement as it becomes the first digital therapeutic authorized for the treatment of major depressive disorder. (https://lnkd.in/d2mggRrH) - Marks a significant milestone as the U.S. Department of Health and Human Services (HHS), under the purview of the Centers for Medicare & Medicaid Services (CMS), announces the finalization of policies aimed at fortifying protections and improving access to care for individuals enrolled in Medicare Advantage and Medicare Part D prescription drug plans. (https://lnkd.in/dbpF3zF5) Stay Informed, Stay Ahead with Market Access Today: marketaccesstoday.com #marketacces #reimbursementpolicies #patientaccessschemes #healthcareindustry #pricing #healtheconomics #pharmacoeconomics #health #pharmaceuticals #medicaldevices #HEOR #HTA #RWE #insights #trends #updates
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