Advertising/Marketing Trends to Expect in Q1 of 2025
Ted Sweetser, VP, Ad Partnerships and Strategy, PurpleLab, identifies advertising/marketing trends he expects in Q1 of 2025.
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Vaccines After COVID: Biopharma's Renewed Public Health and Commercial Push
At the Financial Times’ Global Pharma and Biotech Summit 2024, a panel discussed the potential of mRNA technology in developing cancer vaccines amid distrust from the public.
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Key Findings of the NIAGARA and HIMALAYA Trials
In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
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Biotech Investor Sentiment Climbing Steadily, with Growing Enthusiasm Heading into 2025
The sector’s XBI is up 15% year-to-date; rate cuts, election outcome, and M&A are viewed as tailwinds.
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FDA Approves Johnson & Johnson’s Varipulse for Drug-Resistant Paroxysmal Atrial Fibrillation
The Varipulse platform includes a single-device workflow with minimal to zero fluoroscopy requirements, real-time imaging, and lesion tagging for paroxysmal atrial fibrillation.
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Financial Times Global Pharma and Biotech Summit: The Impact of the Election
How will President Trump’s return to office impact the pharma industry?
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Specialty Value-Based Care is Improving Health Outcomes While Reducing Heath Care Costs
Delivering value-based care is expected to become even more prevalent, driven by factors such as patient comfort with digital tools and advancements in contractual arrangements.
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How to Bring World’s Most Innovative Treatments to Least Wealthy Places
At the Financial Times’ Global Pharma and Biotech Summit 2024, a panel discussed initiatives aimed at bringing cell and gene therapies to low- and middle-income countries.
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Dealmaking and Partnerships: The Future of Financing Innovation
At the Financial Times’ Global Pharma and Biotech Summit 2024, a breakout panel discussed how dealmaking remains vital for biopharma companies facing pipeline and revenue pressures.
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Global Pharma and Biotech Summit: The Impact of Politics on Pharma and Biotech
Amgen CEO Robert A. Bradway discusses the potential impact of the election, and politics in general, will have on the industry.
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Balancing Personalized Targeting with Protecting Consumer Privacy
Ted Sweetser, VP, Ad Partnerships and Strategy, PurpleLab discusses the need to balance personalized targeting with the ethical imperative to protect consumer privacy.
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Pharma Pulse 11/4/24: Community Pharmacies in Crisis, Insights Into ADHD Diagnoses in Adult Women & more
The latest news for pharma industry insiders.
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Viking Therapeutics Presents Positive Data from VK2735 for Reducing Body Weight Effectively and Safely
Results from the VENTURE Phase II trial and a Phase I oral formulation study found that VK2735, a novel a dual GLP-1 and GIP receptor agonist, demonstrated promise in treating obesity.
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Recent Developments in Pharmaceutical Validation
Explore the latest pharmaceutical validation developments with industry experts from Barry-Wehmiller Design Group, Kneat Solutions, and No Deviation. You’ll gain valuable data-driven insights and discover emerging trends from the State of Validation 2024 industry report that are shaping the validation landscape.
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Biopharma Needs a Health System Strategy to Secure Optimal Market Access
In today’s pharmaceutical market access landscape, payers are not the sole decision-makers in utilization management development.
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Pharma Pulse 11/1/24: Navigating Diversity and Digital Innovation, Key Clinical Information on Infertility & more
The latest news for pharma industry insiders.
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Eisai Completes Rolling Biologics License Application to FDA for Subcutaneous Maintenance Dosing Option of Leqembi for Alzheimer Disease
The subcutaneous form of Leqembi was previously granted Fast Track designation by the FDA to treat mild cognitive impairment or mild dementia associated with Alzheimer disease based on data from the Clarity AD study.
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Wegovy Demonstrates Superiority Over Placebo in Patients with Metabolic Dysfunction-Associated Steatohepatitis
Results from Part I of the Phase III ESSENCE trial found that Wegovy 2.4 mg achieved a 37% improvement in liver fibrosis without worsening steatohepatitis in patients with metabolic dysfunction-associated steatohepatitis compared to 22.5% in the placebo group.
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Key Benefits of RWD in Privacy and Targeting Effectiveness
Ted Sweetser, VP, Ad Partnerships and Strategy, PurpleLab discussed how the use of Real-World Data has evolved in the healthcare industry in terms of privacy and targeting effectiveness.
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AbbVie, EvolveImmune Therapeutics Strike Deal to Develop Biotherapeutics for Resistant Cancer Cells
The deal is expected to leverage EvolveImmune’s T-cell engager EVOLVE platform to develop novel antibody-based therapies for solid and hematologic malignancies.
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Expanded Access Treatment Options: Q&S with Johnson and Johnson Innovative Medicine’s Christine MacCracken
The executive director of patient strategies & solutions discusses J&J’s new Guide to Expanded Access.
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Daiichi Sankyo, AstraZeneca Launch Phase III Trials of Datopotamab Deruxtecan in Advanced Nonsquamous Non-Small Cell Lung Cancer
The trials will investigate datopotamab deruxtecan in combination with treatments including rilvegostomig, osimertinib, and chemotherapy in patients with nonsquamous non-small cell lung cancer.
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To Tackle the Plastic Waste Crisis in Pharma, Here’s Where to Start
By demonstrating big advancements in recycling, pharma companies will be much more likely to attract shareholders and other investors, giving themselves a leg up in the competition to lead the biopharmaceutical industry well into the future.
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FDA Approves Protega Pharmaceuticals’ Roxybond for Severe Pain Management
Roxybond is the and only FDA-approved abuse-deterrent immediate-release 10 mg oxycodone formulation designed to reduce abuse of pain medication via intranasal and intravenous routes.
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Long-Term Implications of Ongoing Drug Shortages
Scott Brunner, CEO, and Tenille Davis, Chief Advocacy Officer, of the Alliance for Pharmacy Compounding explore the potential long-term implications of the ongoing drug shortages for the healthcare system and patient care.
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Merck, Moderna Launch Phase III Trial of V940 in Combination with Keytruda for Resectable Non-Small Cell Lung Cancer
Collaboration seeks to advance the treatment of non-small cell lung cancer by combining Keytruda with Moderna’s novel neoantigen therapy, which has shown positive results across cancer types.
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Strengthening Regulatory Framework for Compounded Medications
Scott Brunner, CEO, and Tenille Davis, Chief Advocacy Officer, of the Alliance for Pharmacy Compounding explain how the regulatory framework for compounded medications can be further strengthened to ensure quality and safety, while still maintaining flexibility to address patient needs.
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MDMA Therapy for Mental Health Conditions: Do the Benefits Outweigh the Risks?
Despite a recent FDA Complete Response Letter issued to Lykos for midomafetamine capsules for the treatment of post-traumatic stress disorder, experts believe that the future is bright for psychedelic drugs that treat mental health conditions.
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Fake Weight Loss Drugs: Growing Threat to Consumer Health
In this episode of the Pharmaceutical Executive podcast, UpScriptHealth’s Peter Ax, Founder and CEO, and George Jones, Chief Operations Officer, discuss the issue of counterfeit weight loss drugs, the potential health risks associated with them, increasing access to legitimate weight loss medications and more.
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Pharma Pulse 10/25/24: Improving Site-Sponsor Collaboration, Communication Skills Crucial for Patient Safety & more
The latest news for pharma industry insiders.
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Report: Radiopharmaceutical Market Expected to Reach $26.51 Billion by 2031
Growth is expected due to increased instances of chronic diseases such as cancer and Alzheimer disease.
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AbbVie, Gedeon Richter Ink Deal to Develop Novel Targets for Neuropsychiatric Conditions
Under terms of the deal, Richter will receive an upfront cash payment of $25 million, along with potential future development, regulatory, and commercialization milestones.
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Identifying Illicit Actors vs Compound Pharmacies
Scott Brunner, CEO of the Alliance for Pharmacy Compounding, explains how to identify a compound pharmacy versus and illicit actor.
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The Impact of Artificial Intelligence on the Creation of Medicines
Najat Khan, chief R&D officer, chief commercial officer, Recursion, and Fred Hassan, director, Warburg Pincus, discuss how artificial intelligence can help reduce healthcare costs at the 20th Annual Young & Partners Pharmaceutical Executive Summit held at the Yale Club of New York.
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Pharma Pulse 10/24/24: Safeguarding Customer Data, Price Transparency Reveals Inequities Beyond Patients & more
The latest news for pharma industry insiders.
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Young & Partners Pharmaceutical Executive Summit 2024: Brave New World – Where Are We Heading?
Peter Marks, director, Center for Biologics Evaluation and Research, FDA, presented the keynote presentation on the future of gene therapy as part of the 20th Annual Young & Partners Pharmaceutical Executive Summit held at the Yale Club of New York.
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Qnovia CEO to Speak at Public Meeting with FDA and NIH
The meeting is set to focus on advancing smoking cessation.
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Pharma Marketing Trends to Expect in 2025
In this part of her video interview, Amanda Powers-Han, Chief Marketing Officer, Greater Than One and Pharmaceutical Executive Advisory Board Member identifies marketing trends you expect to be big right away in 2025.
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FDA Approves Allergan Aesthetics’ Botox Cosmetic for Moderate to Severe Vertical Platysma Bands
Regulatory action marks the fourth aesthetic indication and the first beyond facial treatments for Botox.
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Will Pharma Increase Use of Personalized Audio Use in Marketing?
In this part of her video interview, Amanda Powers-Han, Chief Marketing Officer, Greater Than One and Pharmaceutical Executive Advisory Board Member discusses how personalized audio will be utilized within the pharma marketing industry in 2025.
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Johnson & Johnson Details Six Ways it Utilizes AI
The company includes the technology in drug development, improving efficiency, and other areas.
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Healthcare Companies in Florida Partner to Provide Hurricane Relief
Sun Life U.S. teamed up with several other Florida-based companies to provide needed assistance in areas impacted by the recent storms.
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Pharma Pulse 10/18/24: Driving Diversity with the Integrated Research Model, More Treatment Options for Schizophrenia & more
The latest news for pharma industry insiders.
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FDA Approves Expanded Indication for Lumryz in Pediatric Patients with Narcolepsy
Expanded approval of Lumryz offers a once-nightly treatment option for younger patients, eliminating the need for traditional narcolepsy treatments that often require multiple doses throughout the night.
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FDA Grants Priority Review to GSK’s Gepotidacin for Uncomplicated Urinary Tract Infections
Priority Review status for GSK’s New Drug Application for gepotidacin was based on promising results from the Phase III EAGLE-2 and EAGLE-3 trials, which demonstrated non-inferiority to nitrofurantoin in uncomplicated urinary tract infections.
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FDA Approves AbbVie’s Vyalev for Advanced Parkinson Disease
Vyalev is the first and only FDA-approved subcutaneous 24-hour infusion of a levodopa-based therapy for the treatment of motor fluctuations in adults with advanced Parkinson disease.
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Sanofi, Orano Strike Deal to Develop Radioligand Medicines for Rare Cancers
Partnership is expected to develop radioligand therapies based on lead-212 alpha-emitting isotopes, which offer the opportunity to destroy cancer cells with minimal damage to healthy tissue.
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Mirikizumab Demonstrates Superiority to Ustekinumab in Treating Crohn Disease
Results from the Phase III Vivid-1 trial found that more Crohn disease patients treated with mirikizumab achieved histologic response at week 52 compared to ustekinumab.
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Nipocalimab Demonstrates Sustained Disease Control in Adolescents with Generalized Myasthenia Gravis
Results from the Phase II/III Vibrance-MG study found that patients with generalized myasthenia gravis who were treated with nipocalimab plus standard-of-care achieved sustained disease control.
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Assembly Required: Building Blocks in Biopharma
Highlighting two pieces beyond Pharm Exec’s October headliners that draw interesting parallels when it comes to life sciences leadership and building teams and capability internally—whether new businesses or new brands.
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Pharmaceutical Executive: October 2024 Issue (PDF)
Click the title above for a link to open the Pharmaceutical Executive October 2024 issue in an interactive PDF format.
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Rafaat Rahmani: Beating the Odds
Rafaat Rahmani, president and founder of Lifescience Dynamics, grew up in abject poverty, but such hardships—and a later violent brush with racism—would ultimately end up fueling a determined and entrepreneurial path in the life sciences.
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‘Selling a Vision’: Today’s Playbook for Startups
The Big Pharma commercialization playbook doesn’t work for emerging life sciences companies bootstrapping their way up. Exploring three strategies that could be the ingredients of a winning formula for startups.
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Amwins Expands Gene Therapy Coverage
The program will now cover 15 gene and cell therapies.
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Integrating Digital Solutions to Enhance Traceability and Safety in Drug Administration
Laura Johnson, senior director, sales, life sciences, Loftware, discusses integrating digital solutions with traceability and drug administration.
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Amazon Targeting the Transactional in the Pharma Market
A value deficit and potential consumer value proposition.
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Trading Quality for Convenience? The New Tech Balancing Act
Announcements such as Apple’s come with pros and cons for industry.
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FDA Approves Roche’s Itovebi for Endocrine-Resistant, PIK3CA-Mutated Hormone Receptor-Positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer
Approval was based on results from the Phase III INAVO120 trial, which found that Itovebi in combination with palbociclib and fulvestrant significantly improved progression-free survival in patients with endocrine-resistant, PIK3CA-mutated, hormone receptor-positive, HER2-negative locally advanced or metastatic breast cancer.
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How to Rally a Team Around Building a New Business
Three key components to scaling quickly—while maintaining purpose.
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FDA Grants Marketing Authorization for Healgen Scientific’s Home Flu and COVID-19 Combination Test
Healgen’s Rapid Check COVID-19/Flu A&B Antigen Test is the first non-prescription COVID-19/flu combination test to be authorized by the FDA without emergency use authorization.
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Arexvy Demonstrates Sustained Protection From Respiratory Syncytial Virus in Adults Over 60 Years of Age for Three Seasons
Data from the Phase III AReSVi-006 clinical trial found that Arexvy offered a cumulative efficacy of 62.9% against lower respiratory tract disease caused by respiratory syncytial virus.
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DarioHealth Announces Partnership with National Medicare Advantage Plan
The partnership will provide plan members with access to digital services aimed at older patients.
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FDA Grants Breakthrough Therapy Designation to Biogen’s Felzartamab for Late Antibody-Mediated Rejection in Kidney Transplants
Felzartamab granted Breakthrough Designation after a clinical trial showed a significant improvement in late antibody-mediated rejection in kidney transplant recipients compared with placebo.
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FDA Grants Breakthrough Therapy Designation to Boehringer Ingelheim’s Survodutide for Non-Cirrhotic Metabolic Dysfunction-Associated Steatohepatitis
Breakthrough Therapy designation for survodutide was based on preliminary clinical data showing potential improvement in patients with non-cirrhotic metabolic dysfunction-associated steatohepatitis over existing therapies.
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Astellas, AviadoBio Strike Exclusive Option, License Agreement for Potential Treatment for Frontotemporal Dementia
Under terms of the deal, Astellas will obtain the license for the global development and commercialization of AVB-101 to treat frontotemporal dementia with progranulin mutations.
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FDA Approves Increased Dosage of Biofrontera’s Ameluz Topical Gel for Actinic Keratosis
Approval was based on results from Phase I clinical safety studies, which demonstrated that using three tubes of Ameluz maintained similar safety and systemic exposure levels as one tube in treating actinic keratosis in patients undergoing photodynamic therapy.
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AstraZeneca, CSPC Pharmaceutical Group Reach Exclusive Licensing Agreement to Develop Lipid-Lowering Therapy
Under the agreement, AstraZeneca will be granted access to CSPC’s small molecule candidate, YS2302018, with the goal of treating dyslipidemia and cardiovascular disease.
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BCS Financial Introduces Employer Group Gene Therapy Stop Loss
The stop loss is designed to protect against potentially massive costs related to gene therapy treatments.
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Combating Diseases with Limited Investment Incentives: Q&A with Dr. Claire Wagner
Dr. Wagner discusses her work with the Bill and Melinda Gates Medical Research Institute.
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Hologic Launches Breast Cancer Myth Busting Campaign
The campaign is called #BustTheMyth and is aimed at patient education.
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Pharma Pulse 10/4/24: Regulatory Challenges With Data Collection, Poor Sleep Quality Linked to Dementia & more
The latest news for pharma industry insiders.
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FDA Approves Bristol Myers Squibb’s Opdivo in Combination with Chemotherapy for Resectable Non-Small Cell Lung Cancer
Approval for Opdivo was based on results from the CheckMate-77T trial, which demonstrated that the combination significantly improved event-free survival and pathologic complete response in adults with resectable non-small cell lung cancer without EGFR or ALK rearrangements.
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FDA Approves Exact Sciences' Cologuard Plus Non-Invasive Colorectal Cancer Screening Test
Approval of Cologuard Plus follows results from the BLUE-C study, which demonstrated a 95% sensitivity for detecting colorectal cancer.
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Sun Pharma, Philogen Ink Global Commercialization Deal for Fibromun, an Anti-Cancer Immunotherapy
Under terms of the deal, Philogen will complete clinical trials for Fibromun, seek approval, and handle manufacturing, with Sun Pharma leading global commercialization.
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Indegene Digital Summit 2024 (October 17-18)
Indegene Digital Summit 2024 (October 17-18)
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FDA Approves Fresenius Kabi, Formycon’s Stelara Biosimilar for Multiple Inflammatory Diseases
Marketed as a biosimilar to Stelara, approval of Otulfi was based on clinical data demonstrating comparable efficacy in treating inflammatory conditions such as Crohn disease, ulcerative colitis, moderate to severe plaque psoriasis, and active psoriatic arthritis.
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Eli Lilly, Johnson & Johnson Invest in New Drug Manufacturing Facilities
New facilities are expected to focus on manufacturing next-generation medicines and biologic medicines.
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Merck Completes Acquisition of Investigational Bispecific Antibody Therapy from Curon Biopharmaceutical
CN201 is currently being evaluated in Phase I and Phase Ib/II clinical trials for relapsed or refractory non-Hodgkin lymphoma and B-cell acute lymphocytic leukemia.
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Amneal Pharmaceuticals, Metsera Strike Deal to Co-Develop Medicines for Obesity, Metabolic Diseases
Partnership is expected to leverage Amneal’s global manufacturing and product development experience and Metsera’s portfolio of ultra-long acting injectables and oral nutrient-stimulated hormone analogs.
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Commercialization vs. Launch—What You Need to Know
Commercialization vs. Launch—What You Need to Know
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FDA Approves GE HealthCare’s Flyrcado for Diagnosing Coronary Artery Disease
Flyrcado is the first positron emission tomography myocardial perfusion imaging agent of its kind designed for the detection of coronary artery disease.
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Pharma Pulse 9/27/24: Coverage from LogiPharma USA 2024, Payers Looking for Change in Pharmacy Benefits & more
The latest news for pharma industry insiders.
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AAM Names John A. Murphy as CEO
Murphy previously worked at the Biotechnology Innovation Organization as its chief policy officer.
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RxPreferred Launches AI-Powered Savings Program for Members
The program, Rx-Performance, will be available starting in January of next year.
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What is the Secret Sauce for Top School Graduates to Convert Start-Up Ideas into Sustainable Firms?
A Harvard Business School Healthcare Alumni Association Q&A with Martin Gonzalez, Principal of Org and Leadership Development at Google.
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FDA Approves Dupixent as First-Ever Biologic Treatment for Chronic Obstructive Pulmonary Disease
Dupixent was found to significantly reduce the rate of moderate to severe exacerbations of chronic obstructive pulmonary disease, according to data from the Phase III BOREAS and NOTUS trials.
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FDA Approves Bristol Myers Squibb’s Cobenfy for Schizophrenia
Landmark FDA approval of Cobenfy represents the first new class of drugs indicated to treat schizophrenia in decades.
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Study Suggests Semaglutide May Reduce Opioid Overdose Risk in Patients with Type 2 Diabetes
A new JAMA study indicates that semaglutide produced up to a 68% lower risk of opioid overdose for patients with type 2 diabetes compared to other antidiabetic medications.
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Launch Lessons: Bringing a Targeted Oncology Therapy to Market
Omnichannel marketing can help companies improve HCP engagement to facilitate the delivery of effective treatment to patients who desperately need and deserve it.
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Selecting & Developing a Mega Campus
In this part of his Pharmaceutical Executive video interview, Jonathan Scheinberg, of the Northeast Science and Technology Center, identifies key factors that pharmaceutical and biotech companies should consider when selecting and developing mega campuses.
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Securities Litigation Arising from Alzheimer's Drug Treatments
The legal challenges surrounding Biogen’s Aduhelm and Cassava Sciences’ simufilam underscore the ongoing difficulties in Alzheimer’s drug development, leading to securities litigation over allegedly misleading statements about trial results and commercialization efforts.
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FDA Approves Sarclisa for Certain Patients with Multiple Myeloma
The drug is approved for newly diagnosed patients not eligible for transplant and is to be used in combination with standard-of-care treatment.
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Max Colao Shares How OncoVerity is Pioneering Oncology Solutions
Max Colao, CEO of OncoVerity, discusses his extensive experience in the biotech industry and shares how his company is harnessing computational biology and machine learning to develop personalized cancer treatments that aim to reshape the future of oncology care.
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Pharma Pulse 9/23/24: eSource EHR Requirements, Expanding Pharmacy Access & more
The latest news for pharma industry insiders.
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FDA Approves Bimzelx for Psoriatic Arthritis, Non-Radiographic Axial Spondyloarthritis, and Ankylosing Spondylitis
Bimzelx is the first approved medication for active psoriatic arthritis, non-radiographic axial spondyloarthritis, and ankylosing spondylitis that selectively inhibits IL-17A and IL-17F, both of which are key cytokines that drive inflammatory processes.
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Four Key Strategies for Optimizing Your Medical Congress Strategy
Conferences, congresses, and the digital discussions kicked off by those events create a halo effect that amplifies scientific information more so than other scientific activities.
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Global Real World Data Tour: 2024 Key Insights
Webinar Date/Time: Wednesday, October 9th, 2024 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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Bringing Marketing to a New Audience: Q&A with Jeremy Truxal
Truxal discusses Exact Science’s first Spanish language TV commercial and campaign for Cologuard.
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Aflac Launches Campaign for Bridge to Brighter
The program is aimed at raising funds for children with cancer and blood disorders.
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FDA Approves Rybrevant for Locally Advanced, Metastatic Epidermal Growth Factor Receptor Mutated Non-Small Cell Lung Cancer
Rybrevant is the first targeted second-line regimen to significantly reduce the risk of disease progression by more than 50% in patients with locally advanced or metastatic EGFR mutated non-small cell lung cancer, according to Johnson & Johnson.
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Pharma Pulse 9/20/24: The Benefit to Adapting Operating Models, 50% of US Women Skip or Delay Medical Care & more
The latest news for pharma industry insiders.
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Revelation Pharma Launches Nationwide Wholesale Service
The service will provide compounding pharmacy services to healthcare providers.
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Patritumab Deruxtecan Demonstrates Significant Survival Improvement in Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer
Results of the Phase III HERTHENA-Lung02 trial demonstrated the superiority of patritumab deruxtecan over platinum plus pemetrexed induction chemotherapy in patients with locally advanced or metastatic EGFR-mutated non-small cell lung cancer.
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FDA Approves Keytruda Plus Pemetrexed, Platinum Chemotherapy for Unresectable Advanced or Metastatic Malignant Pleural Mesothelioma
Approval was based on data from the IND.227/KEYNOTE-483 trial, which demonstrated a 21% reduction in the risk of death when Keytruda was added to chemotherapy in patients with unresectable advanced or metastatic malignant pleural mesothelioma.
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FDA Approves Fasenra for Eosinophilic Granulomatosis with Polyangiitis
Approval was based on results from the MANDARA Phase III trial, which demonstrated the superiority of Fansenra over Nucala in patients with eosinophilic granulomatosis with polyangiitis.
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Pharmaceutical Executive: September 2024 Issue (PDF)
Click the title above for a link to open the Pharmaceutical Executive September 2024 issue in an interactive PDF format.
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True Digital Surgery Appoints Kevin T. Foley as Chief Medical Officer
As chief medical officer, Foley is expected to guide the clinical direction of True Digital Surgery and the advancement of its Digital Surgical Exoscope Platform.
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FDA Approves Ebglyss for Moderate-to-Severe Atopic Dermatitis
Results from the ADvocate 1, ADvocate 2, and ADhere clinical trials found that patients treated with Ebglyss 38% of patients with moderate-to-severe atopic dermatitis achieved clear or almost-clear skin after 16 weeks of treatment.
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Delivery and Disruption: Navigating a Changing Care Terrain
The diversification of site-of-care delivery models is accelerating rapidly, creating new go-to-market implications for drug manufacturers—but also new opportunities to drive more fundamental innovation in engagement and access strategies.
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CVS Pharmacies to Offer Birth Control Prescribing Services in Massachusetts
These services will help alleviate the impact of contraceptive deserts in the state.
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Rx Power Struggle: How Pharma can Flip the PBM Script
The industry holds the key to true change to the drug access landscape.
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Copay Adjustment Chess Match: What Will Payers Do Next?
As new litigation looms in the debate over use of copay accumulator programs, a look at potential next moves for payers—and steps drug manufacturers should take to ward off cost-driven non-adherence.
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Gilead's Lenacapavir Reduces HIV Infections by 96%, Surpassing Truvada in Twice-Yearly PrEP Treatment
Landmark results from the Phase III PURPOSE 2 trial found that lenacapavir demonstrated 89% greater efficacy than Truvada in preventing HIV infections.
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A Risk-Reward Reset: Getting Serious About Social Media
As the digital medium poses new threats to brand equity and public safety for pharma, what can drugmakers do to better balance its essential communications benefits with the risks?
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FDA Approves Subcutaneous Tecentriq Hybreza for All Adult Indications of IV Form of Tecentriq
Subcutaneous Tecentriq Hybreza will provide patients and physicians increased flexibility for administration of the immunotherapy across approved indications for Tecentriq, including non–small cell lung cancer, small cell lung cancer, and hepatocellular carcinoma.
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Dupixent Demonstrates Reduced Symptoms of Chronic Spontaneous Urticaria
Dupixent displayed a nearly 50% reduction in itch and urticaria activity scores in patients with chronic spontaneous urticaria.
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How UpScriptHealth Guarantees Authenticity & Prevents Counterfeit Drugs from Entering Their Supply Chain
In this part of their Pharmaceutical Executive video interview, UpScriptHealth’s Peter Ax, Founder and CEO, and George Jones, Chief Operations Officer, explain how their company guarantees the authenticity of the medications it dispenses, and the measures are in place to prevent counterfeit drugs from entering their supply chain.
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Report: Obesity Drug Market Estimated to be Worth $200 Billion by 2031
A recent study by Morningstar predicts that 16 new weight-loss drugs could be on the market by 2029.
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Making the Leap from Pharmaceuticals to Private Equity, Venture Capital
A Harvard Business School Healthcare Alumni Association Q&A with Jeremy Goldberg of Arsenal Capital Partners.
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Melissa Krebs Shares GelSana’s Vision for Innovative Wound Care Solutions
In this interview, Melissa Krebs, CEO and founder of GelSana, shares her journey in developing cutting-edge biomaterials that could transform the $78 billion wound care market.
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From Endemic to POC: The Journey Pharma Marketers Need to Tread
The digital revolution has brought more efficient ways to reach and touch HCPs.
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FDA Approves Filspari for Adults with IgA Nephropathy
Filspari is considered the first non-immunosuppressive treatment to significantly slow kidney function decline in adults with IgA nephropathy.
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Fenebrutinib Found Effective in Suppressing Relapsing Multiple Sclerosis Disease Activity
Results of the FENopta study found that after one year of treatment, 96% of patients experienced no relapses of multiple sclerosis, with an annualized relapse rate of just 0.04.
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Beyond the Birthrate: The Societal Costs of Maternal Mortality
Head of Medical Affairs and Outcomes Research at Organon, Charlotte Owens, MD, FACOG, discusses the most critical changes needed to close the gaps in R&D for maternal health solutions and how feasible they are to make.
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Digital Protection: Q&A with Jeffrey Bernstein
Pharma companies are facing a higher number of incredibly destructive cyber-threats than ever before.
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FDA Approves Boruzu for Subcutaneous, Intravenous Administration for Multiple Myeloma, Mantle Cell Lymphoma
Boruzu is the first ready-to-use version of bortezomib for subcutaneous and intravenous administration in the treatment of multiple myeloma and mantle cell lymphoma.
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Potential Treatment Against All COVID Variants
Texas Biomed announced that research shows that a certain monoclonal antibody treatment could treat all variants of COVID-19, including past, present, and future strains.
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Nucala Significantly Reduces Moderate to Severe Exasperations in Chronic Obstructive Pulmonary Disease
Results from the MATINEE trial found that Nucala led to a statistically significant and clinically meaningful reduction in moderate/severe exacerbations of chronic obstructive pulmonary disease compared to placebo over 104 weeks.
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Pharma Pulse 9/6/24: Gaps and Opportunities in Qualitative Systematic Reviews, Companies Grapple With Expanding Cyber Rules & more
The latest news for pharma industry insiders.
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Efsitora Demonstrates Non-Inferiority vs. Insulin Glargine, Degludec for Type 2 Diabetes
Results from the QWINT-1 and QWINT-3 trials found that insulin-naïve patients achieved similar reductions in A1C levels using once-weekly efsitora compared to daily insulin glargine and degludec.
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What is the Transformation Playbook for Moving From Digital Pilot to a Truly Scaled Production Solution?
A C-suite Q&A with Cristina Ortega Duran, President of Evinova.
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High Dose Spinraza Significantly Improves Motor Function in Infants with Spinal Muscular Atrophy
Data from the Phase II/III DEVOTE study demonstrated that Spinraza showed significant motor function improvements at six months in infants with spinal muscular atrophy.
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Moderna Launches New Campaign to Promote COVID Boosters
The “Do It For You & Them” campaign focuses on the impact that virus has on day-to-day lives.
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Lumryz Demonstrates Superiority Over Oxybate Treatments in Narcolepsy
Results of the RESTORE study revealed that 94% of participants preferred Lumryz over twice nightly oxybate treatments for narcolepsy.
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Understanding the Current State of M&A: Q&A with Cheryl Reicin
As the second half of 2024 begins, an industry expert discusses how mergers and acquisitions are trending in the pharma industry.
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Personify Health Offers Employers GLP-1s Best Practices for Coverage Options
The insurance company is offering the guidance in response to continued popularity of the drugs which are commonly used for weight-loss management.
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Radiotherapies: Q&A with Thijs Spoor
Perspective Therapeutics’ CEO explains how this method can be used to determine how to target cancer cells without damaging other organs.
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Embracing FSPs: Q&A with Jenny Denney
Pharmaceutical companies are seeing the benefits of being able to outsource entire functions through functional service providers.
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Revitalizing Mature Pharma Brands: 5 Winning Strategies
Strategies that can help maintain and grow your market share. Plus how to adapt to new competitive pressures and evolving customer needs.
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Ecolab Continues Mission to Protect What's Vital With Deep Investment in Life Sciences
Ecolab is looking to the future with new opportunities to partner with Pharma for critical solutions to support drug development and manufacturing.
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Sanyou Biopharmaceuticals Announces Line of Monkeypox Treatments
The product line includes vaccines, monoclonal antibodies, and antigens.
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Johnson & Johnson Submits Biologics License Application for Nipocalimab in Patients with Antibody-Positive Generalized Myasthenia Gravis
Submission is supported by results from the Phase III Vivacity-MG3 study, which demonstrated that nipocalimab, combined with standard care, significantly improved outcomes for patients with antibody-positive generalized myasthenia gravis.
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Pharma Pulse 8/30/24: Working Towards Greater Access and Diversity, Why 'Normalcy' Is Still a Crisis & more
The latest news for pharma industry insiders.
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FDA Grants Priority Review to Mirdametinib for Neurofibromatosis Type 1-Associated Plexiform Neurofibromas
Submission of a New Drug Application for mirdametinib included data from the Phase IIb ReNeu trial, which evaluated patients with NF1-associated plexiform neurofibromas causing significant morbidity.
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Has Machine Learning Finally Provided Practical Value for the Healthcare Ecosystem?
A Harvard Business School Healthcare Alumni Association Q&A with Dr. Hersh Sagreiya at the Hospital of the University of Pennsylvania.
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Research Growing into the Use of Psychedelics to Treat Substance Abuse
A new National Institutes of Health grant will advance research into the role of the serotonin 5-HT2A receptor in mitigating methamphetamine use.
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Aetna to Cover Fertility Services
This makes Aetna the first major insurer to cover these types of services.
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Lilly Introduces Single-Dose Vials of Zepbound, Expanding Access for Adults with Obesity
The new vials of Zepbound are available through a new self-pay pharmacy channel, priced over 50% lower than other incretin medications for obesity.
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Are We Entering the Nuclear Medicine Industrial Revolution?
Achieving better outcomes for patients and advancing the fields of nuclear medicine and oncology are not just about adopting new technologies, but also about embracing a profound change in how care is delivered.
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Dupixent Demonstrates Efficacy Treating Chronic Obstructive Pulmonary Disease, Asthma
Results from the Phase III BOREAS and NOTUS trials found that Dupixent reduced moderate-to-severe COPD exacerbations by 31% over 52 weeks.
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BioVaxy Announces Findings For Use of DPX in Vaccine Development
The novel lipid-in-oil delivery platform showed positive results across multiple disease states.
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Unlocking the Potential of AI in Healthcare–5 Key Takeaways
The technology has the potential to be implemented across multiple aspects of the industry.
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CDMOs are Exploring Risk-Sharing for Resilient Growth in a BANI World
Key industry trends and how the relationships between companies and CDMOs are evolving to better meet the challenges of a BANI world.
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Addressing Challenges to Access, Advancement of Myeloma Therapies
In an interview with Pharm Exec Associate Editor Don Tracy, Joseph Mikhael, MD, chief medical officer, IMF, discusses challenges of access and advancement of myeloma therapies.
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FDA Approves Updated COVID-19 Vaccines
The updated formulas should provide better protection against the currently circulating strains.
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FDA Grants Fast Track Designation to Clarity Pharmaceuticals’ Novel Treatment for PSMA-Positive Prostate Cancer Lesions
64Cu-SAR-bisPSMA has demonstrated advantages over current diagnostic tools, such as higher tumor uptake, next-day imaging, and a longer half-life in PET imaging of PSMA-positive prostate cancer lesions, Clarity says.
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GLP-1 Therapy Significantly Increases Visceral Adipose Tissue Metabolic Activity in Patients with Obesity, Obstructive Sleep Apnea
Findings from a study published in the Journal of the Obesity Society may significantly advance the understanding of GLP-1 analogues and their role in treating obesity.
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Study Suggests Promise of Psilocybin in Treating Depressive Symptoms
Findings from a recent study demonstrated that high-dose psilocybin provided a superior reduction in depressive symptoms compared to both placebo and escitalopram in patients with major depressive disorder.
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FDA Grants Breakthrough Therapy Designation to GSK’s GSK5764227 for Relapsed or Refractory Extensive-Stage Small-Cell Lung Cancer
Breakthrough therapy designation for GSK5764227 based on preliminary data from the ongoing ARTEMIS-001 Phase I trial, which showed the novel therapy’s promise treating patients with relapsed or refractory extensive-stage small-cell lung cancer.
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FDA Accepts Bristol Myers Squibb’s sBLA for Opdivo and Yervoy Combination for Hepatocellular Carcinoma
Acceptance of supplemental Biologics License Application was based on results from the Phase III CheckMate-9DW trial, which demonstrated that the combination of Opdivo and Yervoy significantly improved overall survival in patients with hepatocellular carcinoma.
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FDA Approves Johnson & Johnson’s Rybrevant and Lazcluze for Advanced Non-Small Cell Lung Cancer
Approval marks the first multitargeted regimen to surpass Tagrisso in efficacy in the first-line treatment of advanced non-small cell lung cancer, according to Johnson & Johnson.
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Johnson & Johnson Set to Acquire V-Wave Ltd
The acquisition, valued at $600 million, is expected to integrate V-Wave into Johnson & Johnson MedTech, which could improve the treatment of heart failure with reduced ejection fraction.
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FDA Approves AstraZeneca’s Imfinzi in Combination with Chemotherapy for Resectable Early-Stage Non-Small Cell Lung Cancer
The combination treatment involves administering Imfinzi with neoadjuvant chemotherapy for non-small cell lung cancer before surgery and as monotherapy post-surgery.
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FDA Approves Incyte and Syndax Pharmaceuticals’ Niktimvo for Treating Chronic Graft-Versus-Host Disease
Approval of Niktimvo was based on positive data from the AGAVE-201 study, which demonstrated a 75% response rate in patients with chronic graft-versus-host disease.
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'Marked’ for Stardom?: Truqap
A breakthrough for biomarker-altered breast cancer—but broader challenges remain.
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Opening the Door: Omvoh
Key approval signals progress in addressing immune-mediated inflammatory diseases.
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A Promising Option: Exxua
Surviving a long road, novel next-generation treatment offers hope for major depressive disorder.
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Divergent Paths: Pharm Exec Profiles Five Recent Drug Launches
Pharm Exec’s latest sampling of notable biopharma brand approvals and launches all have unique stories to tell—from the winding journeys to innovative “firsts” to new momentum for milestones to come.
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An AI Pulse Check
Three pieces of coverage in this month’s issue of Pharmaceutical Executive explore the tipping point that’s seemingly on the cusp in artificial intelligence.
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Pharmaceutical Executive: July/August 2024 Issue (PDF)
Click the title above for a link to open the Pharmaceutical Executive July/August 2024 issue in an interactive PDF format.
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CVS Health Appoints New Chief People Officer
Heidi Capozzi previously served as chief people officer for McDonald’s.
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The Future of Launch Excellence is Generative AI
How drugmakers can reap value from using generative AI in their market-entry strategies and decision-making, including mitigating launch challenges and enhancing the customer conversation.
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Beyond the Buzz: Gauging the True Benefits of AI Today
It’s time to see where artificial intelligence is genuinely being utilized in pharma.
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Big Bets, Bold Steps
Ken Keller, CEO of Daiichi Sankyo’s US business, reflects on the trials, triumphs, and lessons learned in steering the transformation of a legacy cardiovascular company into a global leader in oncology—advancing a vision for a reimagined future in cancer treatment.
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Thriving ‘Beyond the Pill’: Closing Key Gap in Patient Support
Why pharma needs to focus on improving—not just extending life.
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Asia Embracing New Technologies for Better Healthcare
The region is moving to the forefront in integrating therapeutic innovation.
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FDA Issues Complete Response Letter to Lykos Therapeutics for Midomafetamine Capsules in the Treatment of Post-Traumatic Stress Disorder
The Complete Response Letter stated that current data on midomafetamine capsules is insufficient for approval in treating patients with post-traumatic stress disorder.
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AstraZeneca VP, Head of Medical Affairs, US Oncology, Discusses the Impact of PARP Inhibitors on Cancer Treatment
In an interview with Pharm Exec Associate Editor Don Tracy, Carlos Doti, VP, Head of Medical Affairs, US Oncology Business Unit, AstraZeneca, talks PARP inhibitors in cancer treatment and the history of Lynparza.
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Pharma Pulse 8/9/24: AI Companies Fight to Stop California Safety Rules, Building Patient-centric Technology & more
The latest news for pharma industry insiders.
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Finding the Trust in Clinical Trials: Q&A with Lisa Bailey
The Trinity Life Sciences managing director and head of DE&I strategy discusses recent research on the topic.
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Could the Jobs Report Help Reverse Biotech’s Underperformance?
The data may be a catalyst for sector with a now-likely rate pivot looming.
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Merck to Acquire Investigational Bispecific Antibody for B-Cell Associated Diseases From Curon Biopharmaceutical
As part of the acquisition of CN201, Curon is expected to receive an upfront payment of $700 million, with the opportunity to earn an additional $600 million in milestone payments linked to the drug’s development and regulatory approval.
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FDA Approves First Epinephrine Nasal Spray for Type I Allergic Reactions Including Anaphylaxis
Approval of neffy marks a significant advancement in epinephrine delivery, offering a less painful alternative to traditional needle injections.
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FDA Approves Citius Pharmaceuticals’ Lymphir for Relapsed or Refractory Cutaneous T-Cell Lymphoma
Lymphir is the first therapy to target the IL-2 receptor in the treatment of relapsed or refractory cutaneous T-cell lymphoma and the first FDA-approved product for Citius Pharmaceuticals.
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FDA Grants Accelerated Approval to Novartis’ Fabhalta for Primary IgA Nephropathy
Accelerated approval of Fabhalta for treating primary IgA nephropathy was based on positive results from the Phase III APPLAUSE-IgAN study.
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Supportive Oncology Care Shows Promising Results for Patients' Quality of Life: Study
Independence Blue Cross and Jefferson health published a study detailing the impact of such care.
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FDA Approves Medtronic’s Simplera Continuous Glucose Monitor, Announces Partnership with Abbott
Partnership with Abbott for Simplera CGM will expand access to the advanced automated insulin delivery.
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FDA Approves Servier’s Voranigo for Grade 2 IDH-Mutant Glioma
Voranigo is the first targeted therapy in almost 25 years to be approved by the FDA for grade 2 astrocytoma or oligodendroglioma with a susceptible IDH1 or IDH2 mutation following surgery.
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The Impact of Lynparza as a Cancer Treatment
In an interview with Pharm Exec Associate Editor Don Tracy, Carlos Doti, VP, head of medical affairs, US oncology business unit, AstraZeneca, provides an update on current research efforts for Lynparza and discusses its impact on cancer patients over the past decade.
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Pharma Pulse 8/6/24: The Evolution of Temperature-Sensitive Biologics, Is It Bad If AI Kills Meaningless Jobs? & more
The latest news for pharma industry insiders.
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FDA Approves Expanded Indication for Octapharma’s Fibryga for Patients Experiencing Bleeding Due to Acquired Fibrinogen Deficiency
Expanded indication makes Fibryga the first and only on-demand, virus-inactivated, human plasma-derived fibrinogen concentrate approved for this indication.
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FDA Grants De Novo Marketing Authorization to Labcorp’s Genomic Testing Kit
The PGDx elio plasma focus Dx offers laboratories testing options for situations where samples are hard to obtain.
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Informing Organon’s Strategic Approach From an OB-GYN POV
In this part of her Pharmaceutical Executive video interview, Charlotte Owens, MD, FACOG, Head of Medical Affairs and Outcomes Research at Organon, discusses how she’s using her in-practice experience as an OB-GYN to inform Organon’s strategic approach to addressing maternal health challenges.
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Pharma Pulse 8/2/24: Poor Data is a Population Health Risk, Meta’s Earnings Calm AI Jitters & more
The latest news for pharma industry insiders.
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Understanding IDNs and What They Mean to the Pharmaceutical Industry–Q&A with Greg Skalicky
Integrated Delivery Networks have impacted everything from drug launches to sales approaches.
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FDA Expands Approval of GSK’s Jemperli in Combination with Chemotherapy for Adults with Primary Advanced or Recurrent Endometrial Cancer
Approval marks the first time an immuno-oncology regimen has demonstrated a survival benefit for all adults with primary advanced or recurrent endometrial cancer, company says.
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FDA Grants Accelerated Approval to Adaptimmune Therapeutics’ Tecelra for Adults with Synovial Sarcoma Who Have Undergone Prior Chemotherapy
Regulatory action marks the first engineered cell therapy approved for a solid tumor cancer in the United States.
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Blue Shield of California Offers Blue Zones Challenge App to Members
The app provides users with lifestyle tips and plans based on the lifestyles of people living in regions with the highest lifespans.
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Daiichi Sankyo, Merck Launch Phase III Trial Evaluating Safety, Efficacy of Ifinatamab Deruxtecan in Patients with Relapsed Small Cell Lung Cancer
IDeate-Lung02 will compare ifinatamab deruxtecan to a physician’s choice of chemotherapy in patients with relapsed small cell lung cancer.
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AstraZeneca VP, Head of Medical Affairs, US Oncology, Discusses 10 Years of Lynparza Across Eight Indications
In an interview with Pharm Exec Associate Editor Don Tracy, Carlos Doti, VP, head of medical affairs, US oncology business unit, offers his thoughts on the evolution of Lynparza across indications such as breast, prostate, and pancreatic cancers.
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