FDA Approves Takeda’s Subcutaneous Form of Entyvio as a Maintenance Therapy in Adults with Moderately to Severe Crohn Disease
Approval was based on positive data from Takeda’s Phase III VISIBLE 2 study, which displayed long-term clinical remission in approximately half of patients with Crohn disease receiving Entyvio.
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Essential Pharma Acquires Reminyl, a Cholinesterase Inhibitor to Treat Mild to Moderately Severe Dementia from Janssen Pharmaceutica NV
Acquisition includes rights to marketing in the European Economic Area, Thailand, South Korea, and other regions for oral treatment of mild to moderately severe dementia associated with Alzheimer disease.
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Texas Biomed Developing Potential Bird Flu Vaccine
While human infections of the virus are rare, a strain recently appeared in dairy cows before infecting a human in Texas.
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Will Synthetic, AI-Based Digital Humans Change Pharma and Life Sciences? Q&A with Abid Rahman, SVP Innovation, EVERSANA
Rahman discusses the new opportunities that digital twins present to researchers.
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Phase III SELECT-GCA Trial for Rinvoq Yields Promising Results in Treating Patients with Giant Cell Arteritis
According to results of the study, 46% of patients with giant cell arteritis administered Rinvoq achieved sustained remission from weeks 12 to 52.
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Coya Therapeutics CEO Discusses Recent Data Discovery from a Study of Coya 302, a Potential Treatment for ALS
In an interview with Pharm Exec Associate Editor Don Tracy, Howard Berman, Chairman, CEO, Coya Therapeutics, provides an update on the progress of Coya 302 as a treatment for ALS.
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Pharmaceutical Executive: April 2024 Issue (PDF)
Click the title above for a link to open the Pharmaceutical Executive April 2024 issue in an interactive PDF format.
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FDA Approves Stelara Biosimilar Selarsdi to Treat Psoriasis, Psoriatic Arthritis
Alvotech’s and Teva’s Selarsdi (ustekinumab-aekn), the second FDA-approved biosimilar to Stelara, is indicated to treat patients aged 6 years and above with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy and for patients aged 6 years and above with active psoriatic arthritis.
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The IRA Impact: Navigating Its Evolving Complexities
Amid lingering questions and uncertainty, a look at ways pharma companies can prioritize incorporating the Inflation Reduction Act into their strategic planning process—and do it now.
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Pharma Pulse 4/16/24: Mitigating Drug Shortages, PBM Legislation in Washington & more
The latest news for pharma industry insiders.
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Fighting for Innovation
Damien Bailly, president of established markets at Astellas, discusses why partnerships and collaborations are a critical organizational—and wider ecosystem—imperative in ensuring that patients have access to the medicines they need.
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Rare Disease Summit Recap
Greater Than One’s Chief Strategy Officer, Andrew Bast, shares his takeaways from 2024 Rare Disease Summit in Philadelphia, PA.
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Supply Shortages in Weight Loss Drugs
In this Pharmaceutical Executive video interview, Currax Pharmaceuticals, CEO, George Hampton, discusses factors that are contributing to ongoing supply issues and if prices for these therapies are coming down anytime soon.
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Trends in Continuing Medical Education
Elliott Yoo, Senior Media Strategist at epocrates, takes a closer look at the trends in CME consumption and what the future of medical education will be – from the priorities for physicians as they juggle learning with patient care, to what type of activities resonate most with prescribers.
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The Rapid Growth of Remote Patient Monitoring Solutions Can Accelerate Decentralized Clinical Trials
Pharma companies and RPM manufacturers must work together to find solutions to make DCT more commonly available.
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Aspiring for the C-Suite? Consider Being a Chief of Staff
Why this role provides a critical ‘boot camp’ for future pharma leaders.
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Novartis, Arvinas Agree to Strategic Collaboration to Develop Treatment for Prostate Cancer
Partnership also includes an agreement for Arvinas to sell its preclinical AR-V7 program to Novartis.
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Vera Whole Health Announces Launch of Value-Based Primary Care Center in Atlanta
This facility is the first of four facilities to be built in the area.
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FDA Approves New Administration Methods for SK Life Science’s Xcorpi for Adults with Partial-Onset Seizures
New methods allow the antiseizure treatment to be crushed and mixed with water for oral suspension or for use through a nasogastric tube.
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Embedded and agile–The next phase of the DCT evolution
Ellenor discusses key points from the recent SCOPE presentation.
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Invenra, Astellas Launch Partnership Focused on Discovering Therapeutic Bispecific Antibodies
Joint venture aims to implement Invenra’s B-Body bispecific antibody platform to enhance Astellas’ research and development efforts.
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Pfizer Asks FDA to Approve RSV Vaccine for Adults as Young as 18 Years Old
The vaccine is already approved for older adults.
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Lonza, NeuroSense Strike Deal Focused on Exploring Biological Markers for Neurodegenerative Diseases
Collaboration aims to advance the development of treatments for multiple neurodegenerative conditions, including amyotrophic lateral sclerosis.
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Labcorp Announces Expansions to Oncology Portfolio
These expansions include a new product, along with improvements to existing products.
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FDA Approves Expanded Indication for Dovato to Include Adolescent Patients with HIV
Dovato is the first oral, two-drug, single-tablet regimen approved for patients 12 years of age and older who are living with HIV-1.
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Pharma Pulse 4/8/24: Rite Aid Announces Availability of Opill, List Prices for Pharmaceuticals in the US Compared to Other Countries & more
The latest news for pharma industry insiders.
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Pharma Pulse 4/5/24: Patient with Pig Kidney Goes Home, Combining AI and Market Access & more
The latest news for pharma industry insiders.
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FDA Approves Abecma for Patients with Relapsed or Refractory Multiple Myeloma Following Two Prior Lines of Therapy
Abecma was found to triple progression-free survival compared to standard regimens with a 51% decline in the risk of disease progression or death in patients with relapsed or refractory multiple myeloma who were previously administered two or more lines of therapy.
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A Decade of Data Under the Belt
In this Pharmaceutical Executive video interview, Currax Pharmaceuticals, CEO, George Hampton, discusses their drug Contrave and the data they have to show after a 10 years in the weight loss/obesity space.
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Amylyx Begins Process of Discontinuing Relyvrio/Albrioza for Treatment of ALS
Decision to discontinue marketing authorizations for Relyvrio/Albrioza comes as a result of topline results from the Phase III PHOENIX trial in patients with amyotrophic lateral sclerosis.
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Johnson & Johnson Set to Acquire Shockwave Medical, Aiming to Strengthen Company’s MedTech Division
The deal, which is worth approximately $13.1 billion, is part of J&J MedTech’s goal to expand into high-growth markets.
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QuantalX Joins FDA’s Total Life Cycle Advisory Program
FDA’s program will provide guidance to the development of the company’s Delphi-MD technology.
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Moderna Releases Promising Data from Phase I/II Clinical Trial on mRNA-3927 for Propionic Acidemia
Early results have demonstrated that mRNA-3927 has led to a 70% reduction in the relative risk for metabolic decompensation events in patients with propionic acidemia.
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CVS Health Announces New Offerings for Pharmacy Students
The two programs will be offered to students and CVS interns.
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FDA Approves Vanda Pharmaceuticals' Fanapt to Treat Adults with Bipolar I Disorder
Fanapt was previously approved by the FDA in 2009 as an antipsychotic treatment for schizophrenia.
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Non-Gene Edited Therapeutics: Q&A with Jeffrey Erickson, Vice President of Business Development at Triumvira
Erickson discusses his work developing unique, targeted autologous and allogeneic T cell therapeutics.
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FDA Approves Abbott’s i-STAT TBI Whole Blood Rapid Test to Assess Patients for Concussions at Bedside
The concussion test, which shows results after 15 minutes, can help evaluate patients up to 24 hours after injury, company says.
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Pharma Pulse 4/2/24: Bird Flu in Texas, Anxiety/Depression Treatment Linked with Heart Disease Outcomes & more
The latest news for pharma industry insiders.
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Mishe Announces Omnichannel Pharmacy Network
The network will work with DiRx and MakoRX.
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President of Petros Pharmaceuticals Discusses the Future of OTC Contraceptives
In an interview with Pharm Exec Associate Editor Don Tracy, Fady Boctor, President, Chief Commercial Officer, Petros Pharmaceuticals provides his thoughts on what the future looks like when it comes to over-the-counter (OTC) contraceptives.
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Pharma Pulse 3/29/24: Super Micro’s AI Boom Carries a Big Price Tag, Leveraging Digital Tools to Optimize Manufacturing & more
The latest news for pharma industry insiders.
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Gilead, Xilio Therapeutics Ink Exclusive Licensing Agreement to Develop Early Phase Tumor-Activated IL-12
Deal aims to commercialize XTX301 for treating advanced solid tumors by leveraging Xilio’s tumor-activated immuno-oncology therapies.
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FDA Hands Expanded Indication to Gilead’s Vemlidy for Chronic HBV Infection in Pediatric Patients
Phase II clinical study showed that children as young as six years of age with hepatitis B virus could benefit from treatment with Vemlidy.
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Researchers Present First Study Using Biomimetic AI Digital Twins
The study used technology developed by a variety of companies, including RYLTI.
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Pfizer Makes Publicis New Global Creative Duties Partner
The news comes less than a year after Pfizer announced that IPG would handle this role.
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Fierce Females in the Life Science Space
In this week’s episode, in recognition of international women’s month, Editor Miranda Schmalfuhs has compiled audio clips from interviews with female KOLs that she’s been fortunate enough to speak with over this past month for content across a few of our brands.
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FDA Grants 501(k) to Two Avicenna.AI Products
Both products are designed to help radiologists.
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Beyond the Scrubs: Understanding Healthcare Providers as People for Increased Engagement
The benefits of adopting a humanized approach to healthcare provider marketing extend across the healthcare spectrum, enhancing engagement rates, brand loyalty, and marketing ROI, while also driving better outcomes for patients.
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FDA Approves Roche’s Cobas Malaria Test, Designed to Screen for Malaria in Potential Blood Donors
Action marks the first FDA-approved blood screening test for malaria.
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Pharma Pulse 3/27/24: Patients Hate ‘Forever’ Drugs—Is Wegovy Different? Low Melatonin Can Increase Risk of Neurological Disorders & more
The latest news for pharma industry insiders.
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Viking Therapeutics Reveals Positive Results from Oral Obesity Drug
Reportedly, the oral weight loss pill VK2735 showed promising signs of effectiveness and a tolerable safety profile.
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Operating Models for Successful DOL Engagement
How life sciences companies can design an effective operating model for DOL engagements.
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FDA Approves AstraZeneca’s Ultomiris for Neuromyelitis Optica Spectrum Disorder
Action marks the first FDA approval of a long-acting treatment for adult patients with neuromyelitis optica spectrum disorder who are positive for the anti-aquaporin-4 antibody.
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Influencer Marketing, Digital Opinion Leaders
How consumer goods marketing approaches can support pharmaceutical and life sciences companies in their growth this year.
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Pharma Pulse 3/22/24: Surgeons Transplant Pig Kidney into a Patient, Effective Ways to Engage Patients, Caregivers, and Advocacy Groups & more
The latest news for pharma industry insiders.
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FDA Approves Italfarmaco SpA’s Duvyzat for Duchenne Muscular Dystrophy
Duvyzat (givinostat) is histone deacetylase inhibitor that was previously granted priority review, orphan drug designation, and rare pediatric disease designation by the FDA for patients 6 years of age and older with Duchenne muscular dystrophy.
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Addressing Unmet Needs in Schizophrenia, Pulmonary Arterial Hypertension & NASH
In this Pharmaceutical Executive video interview, Optum Rx clinical pharmacist, Arash Sadeghi, discusses the three drugs featured in their Drug Pipeline Insights Report for 2024 and which unmet needs they address.
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Clinical Trial of Keytruda and Lynparza Combination Fails to Meet Primary Endpoint for Treatment of Metastatic Nonsquamous Non-Small Cell Lung Cancer
Despite not having a positive outcome, safety profiles for Keytruda and Lynparza were consistent with previous findings.
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Medicare to Cover Wegovy for Certain Indications
The drug was recently cleared to treat cardiovascular risks, making it eligible for Medicare Part D.
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CDC Releases Health Alert and Pushes for Increase in Measles Vaccinations
The agency released guidelines for vaccinations guidelines for children as young as 6 months old.
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Research Lab Unveils Tool to Improve Clinical Trial Participation
Cold Spring Harbor Laboratory details how the new tool will help reduce common barriers to trial participation.
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OncoHost Wins AI Excellence Award
The technology platform won the award for its work using AI to improve precision medicine.
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Cambrex Plans to Complete $100 Million Investment Strategy Earlier Then Planned
The company will see the completion of its projects about a year earlier than expected.
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FDA Grants Accelerated Approval to Takeda's Iclusig for Ph-Positive Acute Lymphoblastic Leukemia
Label expansion approval for Iclusig (ponatinib) addresses adult patients with newly diagnosed Philadelphia chromosome–positive acute lymphoblastic leukemia.
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Lunit Expands AI Cancer Screening to France and Portugal
The company’s software will be used to help with chest and breast cancer screenings.
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FDA’s Oncologic Drugs Advisory Committee Recommends Earlier Treatment with Carvykti for Relapsed or Refractory Multiple Myeloma
In a unanimous decision, the committee recommended Carvykti based on promising data from the Phase III CARTITUDE-4 study, which showed a positive risk-benefit assessment.
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BeiGene and Leukemia & Lymphoma Society Sign Three Year Agreement
As part of the partnership, BeiGene will serve as a sponsor at LLS events.
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Pharma Pulse 3/15/24:Pharma Dealt Loss Over Discount Program, Adopting New Manufacturing Technologies & more
The latest news for pharma industry insiders.
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FDA Approves First Treatment for Noncirrhotic Nonalcoholic Steatohepatitis (NASH)
Madrigal Pharmaceuticals’ Rezdiffra (resmetirom) was granted accelerated approval for the treatment of adult patients with noncirrhotic nonalcoholic steatohepatitis (NASH).
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FDA Grants Accelerated Approval to Bristol Myers Squibb’s Breyanzi for Relapsed or Refractory CLL, SLL
CAR T-cell therapy Breyanzi (lisocabtagene maraleucel) approved for adults with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who were previously administered at least two lines of therapy.
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FDA Approves Tevimbra, BeiGene’s Treatment for Adults with Unresectable or Metastatic Esophageal Squamous Carcinoma
Tevimbra (tislelizumab-jsgr) has been approved as a monotherapy for adult patients with unresectable or metastatic esophageal squamous cell carcinoma who have previously undergone systemic chemotherapy excluding PD-L1 inhibitors.
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Hurdles Hindering the Translation of AI-Powered Research into Tangible Clinical Benefits
In this Pharmaceutical Executive video interview, Murray Aitken, Executive Director of the IQVIA Institute for Human Data Science, discusses why no novel active substances have yet been brought to market through AI technology despite increasing investments in the space for drug discovery as shown in IQVIA’s Global Trends in R&D 2024 report.
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How AI Could Have Helped Past Challenges
In this Pharmaceutical Executive video interview, Kaveh Vahdat, Founder and President of RiseOpp, discusses how AI could have helped address past challenges.
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AstraZeneca Acquires Amolyt Pharma with the Aim of Developing Rare Endocrine Disease Treatments
Acquisition is highlighted by eneboparatide, Amolyt’s Phase III peptide for hypoparathyroidism with a novel mechanism of action.
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How’s Business?
The new season could bring with it more possibilities for renewal in the biotech sector, as our coverage this month highlights.
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Par Pharmaceutical Issues Recall of Single Lot of Treprostinil
The voluntary recall was ordered due to potential silicon particulate exposure.
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Putting Menopause Medication on the Main Stage
In this Pharmaceutical Executive interview, Jill Jaroch, Senior Director, Women’s Health & Urology Marketing at Astellas, discusses the decision to continue VEOZAH’s presence during the big game, the inspiration and message behind the commercial, and if Taylor Swift played a factor in their decision making
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Positioning Medical Information as a Trust Driver for Your Brand
Four steps to maximize the impact of medical information services as an engagement gateway.
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Contributing Factors to the Growing Gap in Access Between the US and Europe
In this Pharmaceutical Executive video interview, Murray Aitken, Executive Director of the IQVIA Institute for Human Data Science, discusses findings from IQVIA’s Global Trends in R&D 2024 report that shows why the US continued to lead in new drug launches in 2023.
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FDA Approves Expanded Indication for Praluent to Lower LDL-C in Pediatric Patients with HeFH
Regeneron’s PCSK9 inhibitor approved to reduce low-density lipoprotein cholesterol in patients 8 years of age and older with heterozygous familial hypercholesterolemia.
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Boehringer Ingelheim Unveils New Out-of-Pocket Cap Initiative for its Inhaler Product Portfolio
Starting June 1, Boehringer Ingelheim plans to cap inhaler products for respiratory diseases at $35 per month for eligible patients.
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FDA Grants Accelerated Approval to Brukinsa Plus Gazyva for Relapsed or Refractory Follicular Lymphoma
BeiGene’s Brukinsa is a small molecule Bruton’s tyrosine kinase inhibitor indicated as a monotherapy and in combination with other treatments for various B-cell malignancies.
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Approval of Eli Lilly's Alzheimer Drug Donanemab Delayed as FDA Seeks More Information
Because of the unique trial design of the Phase III TRAILBLAZER-ALZ 2 study, the FDA is seeking additional input regarding the safety and efficacy of donanemab for the treatment of early symptomatic Alzheimer disease.
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How Data Integrity Landscape Will Evolve Over the Five Years
In this Pharmaceutical Executive video interview, Daniel Ayala, Chief Security and Trust Officer, Dotmatics discusses how the data integrity landscape will evolve over the next five years and what extent bench scientists in the lab focused on data integrity.
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FDA Approves Expanded Indication for Wegovy to Lower Cardiovascular Risk in Adults with Heart Disease, Obesity
FDA approves Wegovy (semaglutide) to lower the risk of major adverse cardiovascular events in adults with known heart disease and with either obesity or overweight, in addition to a reduced calorie diet and increased physical activity.
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Relyvrio Falls Short of Primary Endpoint in Phase III PHOENIX Trial in Patients with ALS
Relyvrio did not significantly alter amyotrophic lateral sclerosis disease progression as measured by the ALSFRS-R total score at Week 48 compared to placebo.
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FDA Approves Opdivo Plus Chemotherapy for Frontline Treatment of Unresectable, Metastatic Urothelial Carcinoma
Opdivo (nivolumab) plus cisplatin and gemcitabine was found to improve overall survival and progression-free survival compared with chemotherapy alone in patients with unresectable or metastatic urothelial carcinoma.
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Gilead, Merus Strike Deal to Develop Novel Trispecific T-Cell Antibodies for Cancer Treatment
Agreement to focus on research, option, and licensing for discovery of dual tumor-associated antigen-targeting antibodies.
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Bayer Won’t Be Splitting Up
The company plans to spend the coming years strengthening its market position and pipeline while also clearing its issues with litigation and debt.
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FDA Approves Pair of Interchangeable Denosumab Biosimilars
The biosimilars Wyost and Jubbonti (denosumab-bddz) were approved as interchangeable products for Prolia and Xgeva for the treatment of osteoporosis, hypercalcemia, and to prevent skeletal-related events associated with bone metastases from solid tumors.
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Bringing Neuroplastogens to the Window: Q&A With Delix CEO Mark Rus
Rus discusses his company’s work with neuroplastogens and how they differ from similar, psychedelic treatments.
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How the Pandemic Changed the Way Pharma Looks at Data Integrity in 2024
In this Pharmaceutical Executive video interview, Daniel Ayala, Chief Security and Trust Officer, Dotmatics, discusses data security threats from human error to AI tech and how COVID-19 impacted data integrity.
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Amring Changes Name to Nordic Pharma, Inc. Amid Ownership Change
Rebranding aims to align company with its parent company and other subsidiaries.
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Indapta Therapeutics Granted FDA Fast Track Designation for Natural Killer Cell Therapy for Hematologic Malignancies
IDP-023 is a highly potent natural killer cell platform under evaluation for patients with multiple myeloma and non-Hodgkin lymphoma.
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CDC’s Advisory Committee Recommends Another Round of Covid-19 Shots for Seniors
The agency updated its recommendations after a vote by the ACIP advisory committee.
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The State of Obesity-Related Clinical Research: Q&A with Simon Bruce, Vice President, Internal Medicine, Drug Development Solutions, ICON
Simon discusses a recent survey ICON conducted with professionals in obesity-related clinical research.
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Bristol Myers Squibb Reveals Promising Results from Trial of Zeposia for Multiple Sclerosis
Phase III DAYBREAK study found consistent safety with Zeposia in patients with relapsing forms of multiple sclerosis.
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CMS Signals Looming Sunshine Act Audits: How to Prepare
New guidance suggests that CMS may be ramping up Sunshine Act auditing activities, potentially resulting in monetary liability for noncompliant reporting entities.
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With the Rise of GLP-1 Agonists for Treating Obesity, Will Access Challenges Prevent Progress?
JAMA commentary suggests that issues such as high costs, access, and equity will stop patients from obtaining GLP-1 agonists to treat obesity.
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FDA and Workflow Services Detail First 100 Days of Data Collection Partnership
The agency teamed up with the software company to develop platforms and networks to collect de-identified data.
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Biosimilars Report Shows Challenges, Opportunities Across Disease States
Cardinal Health report highlights new biosimilar treatments, legislative developments, and multiple industry perspectives.
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Viking Therapeutics’ GLP-1/GIP Receptor Agonist Shows Positive Results in Obesity Clinical Trial
The trial reportedly showcased significant weight reduction in those treated with VK2735, a dual GLP-1/GIP receptor agonist.
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AbbVie, OSE Immunotherapeutics Strike Deal to Develop Monoclonal Antibody for Chronic Inflammation
OSE-230 was developed to activate a unique mechanism for resolving chronic inflammation, focusing on modulation of macrophages and neutrophils.
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FDA Approves Imbruvica Label Expansion to Include Oral Suspension Formulation
New label marks the first Bruton’s tyrosine kinase inhibitor to be approved with an oral suspension formulation.
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Allecra Therapeutics' Exblifep Approved by FDA for Complicated Urinary Tract Infections
The FDA granted Allecra with a five-year marketing exclusivity extension for Exblifep (cefepime/enmetazobactam) through the Generating Antibiotic Incentives Now Act.
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GSK Reports Promising Results from Clinical Trial of Oral Antibiotic for Uncomplicated Urogenital Gonorrhea.
In the EAGLE-1 Phase III trial, gepotidacin met the primary efficacy endpoint of non-inferiorty to the current leading treatment for uncomplicated urogenital gonorrhea.
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Asthma Medication Xolair May Reduce Peanut Allergies, New Study Finds
FDA has approved the medication in adults and children with allergies.
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IQVIA Executive Director Discusses Global Use of Medicines 2024 Report – Part 1
Murray Aitken, Executive Director of the IQVIA Institute for Human Data Science, discusses key findings from their Global Use of Medicines 2024 report as well as the significant projected growth in spending and growth in diabetes and global obesity
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HLTH Inc. and GE Healthcare Reveal Healthcare-Themed Art Gallery
The gallery will be a part of the HLTH Europe event and will be open to all attendees.
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FDA Grants Priority Review to Dupixent for Uncontrolled Chronic Obstructive Pulmonary Disease
The FDA has assigned a supplemental Biologics License Application submitted by Regeneron and Sanofi for Dupixent in the treatment of COPD with type 2 inflammation with a PDUFA date of June 27, 2024.
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Frontier Medicines Announces Series C Funding to Advance Development of Next Generation KRAS Blocker
Funds expected to advance multiple programs into clinical studies, including FMC-376, which targets KRASG12C cancers.
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NIH Study Estimates Pfizer’s Paxlovid Could Reduce COVID-19 Hospitalizations, Saving Billions in Healthcare Costs
Results of a study conducted by the National Institutes of Health indicate that the Paxlovid prevented a substantial number of hospitalizations associated with COVID-19.
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FDA Warns Against Using Smartwatches or Smart Rings to Measure Blood Glucose Levels
The agency issued a statement reminding the public that it has not approved any such devices for this use.
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Study Finds Parkinson Disease Drug Nearly Matches Wegovy in Weight Loss Effects
Early-stage trial results indicate that NLRP3 inflammasome inhibitors were able to achieve nearly the same weight loss as Wegovy while also reducing inflammatory biomarkers linked to heart disease.
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Senators Pen Letter to FDA Urging Stronger Enforcement on Deceptive Direct-to-Consumer Social Media Ads Promoting Prescription Drugs
Letter emphasizes the need to protect children from potentially harmful medical advice spread on social media.
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Regeneron's Linvoseltamab Granted FDA Priority Review for Relapsed/Refractory Multiple Myeloma
The FDA assigned the biologics license application for linvoseltamab to treat relapsed/refractory multiple myeloma with a Prescription Drug User Fee Act of August 22, 2024.
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AbbVie’s CEO Announces Retirement, To Be Succeeded by Robert A. Michael
The previous CEO, Richard A. Gonzalez, has served as CEO since 2013.
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WuXi Advanced Therapies’ Philadelphia Site Approved by FDA to Start Manufacturing Iovance’s Melanoma T-cell Therapy
Amtagvi is the first one-time, individualized T-cell therapy approved by the FDA for any solid tumor cancer.
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The Shifting Landscape of the Life Sciences Job Market
Planning for a post-recession scenario is essential, ensuring companies are prepared to scale up when funding permits.
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AstraZeneca’s Tagrisso With Chemotherapy Gets FDA Approval for EGFR-Mutated Non-Small Cell Lung Cancer
The FDA has also approved Tagrisso (osimertinib) as a monotherapy for the first-line treatment of patients with locally advanced or metastatic EGFR-mutated non-small cell lung cancer (NSCLC), locally advanced or metastatic EGFR T790M mutation-positive NSCLC, and adjuvant treatment of early-stage EGFRm NSCLC.
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Copay Adjustment Programs: What’s Next for Manufacturers?
Amid shifting healthcare cost strategies, how manufacturers can apply past lessons to best support patients and help boost drug adherence.
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Study Shows Potential of Artificial Intelligence in Predicting Responses to Treatment for Major Depressive Disorder
Investigators harness machine learning to evaluate response to sertraline treatment for major depressive disorder.
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Cultivating a Bespoke Recruitment Strategy for Your FSP Partnership
How a multipronged approach to staff recruitment can accelerate trial success.
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FDA Grants Traditional Approval to Tepmetko for Metastatic Non–Small Cell Lung Cancer
The FDA previously granted accelerated approval to Tepmetko for metastatic non–small cell lung cancer harboring MET exon 14 skipping alterations.
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Cancer & Work: Acting Together: An Interview With Raj Verma, Chief Diversity, Culture, and Experience Officer at Sanofi
In an interview with Pharm Exec Associate Editor Don Tracy, Raj Verma, Chief Diversity, Culture, and Experience Officer, Sanofi, discusses features of the company’s support program for patients diagnosed with cancer and other critical illnesses.
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Xolair Approved by FDA as First Treatment for Multiple Food Allergies in Adult, Pediatric Patients
Novartis’ and Roche’s Xolair (omalizumab) is indicated to treat severe allergic reactions after accidental exposure to one or more foods in individuals aged one year and above.
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Digging Deeper Into Bayer’s ASCO GU Presentation
Iris Kuss, head of clinical development, and Jorge Ortiz, head of medical affairs, discuss the company’s recent presentation at ASCO GU.
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GSK Completes Acquisition of Aiolos Bio
This acquisition will add asthma treatment A1O-001 to GSK’s portfolio.
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Citius Pharmaceuticals Resubmits BLA for Lymphir to Address FDA Complete Response Letter
Lymphir is an immunotherapy under evaluation for the treatment of patients with relapsed/refractory cutaneous T-cell lymphoma following at least one previous line of systemic therapy.
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Aurlumyn Becomes First Severe Frostbite Medication to Receive FDA Approval
Treatment aims to reduce the risk of finger or toe amputation due to frostbite.
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FDA Approves Ipsen’s Onivyde Combination for Metastatic Pancreatic Adenocarcinoma
Pancreatic adenocarcinoma is the most common form of pancreatic cancer, with more than 60,000 diagnoses per year in the United States.
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Roche Ends Agreement With Repare Therapeutics to Develop ATR Inhibitor Camonsertib
Roche halts agreement with Repare Therapeutics to develop and commercialize camonsertib just weeks after triggering a $40 million milestone payment when the first patient was dosed with the novel cancer drug.
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Building Resiliency: Essential Leadership Principles for 2024
Embracing business imperatives such as operational efficiency and a focus on a patient-centric approach can help pharma leaders provide a stable foundation amid lingering uncertainty.
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FDA Fast Tracks GSK's Bepirovirsen for Chronic Hepatitis B Virus
In clinical trials, bepirovirsen showed the potential to address a significant unmet medical need for patients with chronic hepatitis B by reducing hepatitis B surface antigen levels and HBV DNA.
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Using AI to Solve Drug Shortage Issues
In this video interview with Pharm Exec Associate Editor Miranda Schmalfuhs, Dr. Jo Varshney, CEO & Founder of VeriSIMLife, discusses how artificial intelligence and machine learning can assist in the drug shortage problem.
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How to Stand Out in the Wellness Space as a Pharma Brand
Key steps in relationship-building beyond just treatment options.
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Takeda's TAK-861 Shows Promising Results in Phase IIb Trial for Narcolepsy Type 1
Novel oral orexin receptor 2 agonist produced statistically significant and clinically meaningful improvements in wakefulness compared with placebo in patients with narcolepsy type 1.
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Samgsung Biologics, LegoChem Biosciences Partner on Development of Antibody-Drug Conjugate
Joint venture aims to submit an Investigational New Drug application to the FDA by early next year for treatment that targets solid tumors.
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The Promise and Peril of AI in the Physical World
The use of artificial intelligence (AI) in drug development has been hampered by issues that have caused a gap between AI’s potential and its full utilization in this space.
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New Report Says Generic Drug Market Is Set to Grow Over $175 Billion by 2027
According to the study conducted by Technavio, North America will contribute to 37% of the expected growth.
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BioNTech and Autolus Announce Strategic Alliance to Bolster CAR-T Cell Pipeline
BioNTech will invest $200 million and get access to Autolus’ manufacturing sites.
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2024 Life Sciences Accounting & Reporting Congress
2024 Life Sciences Accounting & Reporting Congress
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Johnson & Johnson’s Novel Targeted Oral Peptide Shines in Phase II Trial for Plaque Psoriasis
JNJ-2113, an oral IL-23–receptor antagonist peptide, showed consistency across clinician and patient-reported outcomes in patients with moderate-to-severe plaque psoriasis.
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Gilead Discontinuing Development of Magrolimab in Hematologic Cancers Following Full Clinical Hold by FDA for Increased Risk of Death
Data from the ENHANCE-3 trial of magrolimab in combination with azacitidine plus Venclexta showed futility and an increased risk of death in patients with acute myeloid leukemia.
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Bristol Myers Squibb Seeks Approval for Opdivo Regimen in Resectable Non-Small Cell Lung Cancer
Results from the Phase III CheckMate -77T trial show that Opdivo (nivolumab) plus chemotherapy followed by surgery and adjuvant Opdivo produced statistically significant and clinically meaningful improvements in event-free survival in patients with resectable stage IIA to IIIB non-small cell lung cancer.
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Amgen's Novel Weight Loss Drug Shows Potential for Longer Lasting Effect With Less Frequent Dosing Than Wegovy, Zepbound
In a Phase I trial, data suggest that Amgen’s maridebart cafraglutide (MariTide) may allow patients to take lower and less frequent doses over time while still maintaining significant weight loss.
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FDA Fast Tracks Antibody-Drug Conjugate for Epithelial, Fallopian Tube, Primary Peritoneal Cancers
BioNTech SE and Duality Biologics’ next-generation antibody-drug conjugate is being evaluated for patients with platinum-resistant ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer previously administered one to three systemic treatment regimens.
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Synchron, Potential Competitor to Elon Musk’s Neuralink, Obtains Equity Interest in Acquandas to Accelerate Development of Brain-Computer Interface
Synchron’s brain-computer interface device is being developed to allow patients with mobility challenges to operate certain technology with their mind.
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Beyond Images: 2024 Trends Reshaping Healthcare with Radiopharmaceuticals
By capitalizing on AI advancements, pushing the boundaries of personalized medicine with theranostics, and strengthening digital healthcare networks, radiopharmaceuticals are poised to transform healthcare from a reactive to a proactive discipline.
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Novartis Terminates Licensing Rights With Allarity for Cancer Drug Due to Missed Payments
Novartis rescinds rights to to develop and commercialize multi-tyrosine kinase inhibitor dovitinib due to a material breach by Allarity for lack of financial payment.
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Novo Nordisk Increases Supply of Lower-Dose Wegovy to Meet Continued Demand
The company has struggled to supply the drug to patients due to overwhelming popularity.
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FDA Issues Warning of Contaminated Copycat Eyedrops
The agency issued the warning against three brands of unapproved eyedrops designed to look like an approved brand.
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Sanofi Announces New Reservation Program to Mitigate Shortages of RSV Vaccine for Next Season
Beyfortus (nirsevimab-alip), a monoclonal antibody that protects against respiratory syncytial virus-associated lower respiratory tract disease, experienced higher than anticipated demand that led to shortages during the 2023-2024 season.
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Shubh Goel, VP, Head of Immuno-Oncology and Gastrointestinal Tumors Franchise, US Oncology Business Unit, AstraZeneca, Discusses Positive Results From Phase III Trial In Patients With HCC
In an interview with Pharm Exec Associate Editor Don Tracy, Shubh Goel, Head of Immuno-Oncology and Gastrointestinal Tumors, US Oncology Business Unit, AstraZeneca, provides her thoughts on the success of the trial.
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CDC STI Surveillance Report Finds Over 2.5 Million Cases of Sexually Transmitted Infections, Skyrocketing Rates of Syphilis
The US Department of Health and Human Services has initiated a comprehensive strategy to address the escalating syphilis rates, as a result.
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DELFI Diagnostics Launches Assay That May Improve Monitoring of Cancer Treatment Response
DELFI-Tumor Fraction assay was developed to improve noninvasive assessment of tumor burden and monitoring of treatment efficacy and resistance in patients with advanced cancers.
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Veracity Benefits, Levrx Technology Reveal New Digital Health Tech App
App aims to leverage digital technology to significantly reduce pharmacy costs.
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Biogen Pulls Plug on Controversial Alzheimer Disease Drug Aduhelm
Aduhelm (aducanumab-avwa) was granted accelerated approval by the FDA in June 2021 despite misgivings from the agency’s Peripheral and Central Nervous System Drugs Advisory Committee.
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New Lilly Marketing Campaign Highlights Patient Challenges in Road to Recovery
Eli Lilly advertisement emphasizes that advancements in in medicine can lead to improved population health.
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Bristol Myers Squibb's Breyanzi Granted FDA Priority Review for R/R Follicular Lymphoma, Mantle Cell Lymphoma
CAR T-cell therapy Breyanzi (lisocabtagene maraleucel) to be evaluated in patients with relapsed or refractory follicular lymphoma and mantle cell lymphoma following treatment with a Bruton tyrosine kinase inhibitor.
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FDA Approves Takeda's Gammagard Liquid for Chronic Inflammatory Demyelinating Polyneuropathy
This is Takeda’s second approval in chronic inflammatory demyelinating polyneuropathy this month after the FDA approved HyQvia to protect against relapse of neuromuscular disability and impairment in this patient population.
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EMA Grants Bersiporocin Orphan Drug Designation
The agency recognized the medication as a significant advancement for the treatment of IPF.
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FDA Grants Priority Review to AstraZeneca and Daiichi Sankyo's Enhertu for HER2+ Solid Tumors
Enhertu has been approved by the FDA for indications in breast cancer, non-small cell lung cancer, and gastroesophageal junction adenocarcinoma.
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Report: Three US Residents Suffering from Hypoglycemia Used Suspected Counterfeit Ozempic
Report comes after the FDA seized thousands of counterfeit Ozempic units.
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Combating the Opioid Crisis With Long-Acting Injectables
Substance use disorder is a complex condition that demands innovative solutions, one of which that has shown promise is the use of long-acting injectables.
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Recent Licensing Agreement Poised to Advance Company ADC
In an interview with PharmExec Associate Editor Don Tracy, Jingsong Wang discusses Nona Biosciences’ recent exclusive license agreement with Pfizer Inc. for the development and commercialization of HBM9033.
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GLP-1 Agonists May Lower Cirrhosis, Liver Cancer Risk in Type 2 Diabetes Patients
Study finds that individuals who took GLP-1 agonists for a long duration had a lower risk of going on to develop more severe forms of liver disease, including cirrhosis and liver cancer.
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Citing Severe Health Risks, FDA Issues Warning Against Using Tianeptine Products
Atypical antidepressant linked to severe adverse effects and death as a result of misuse.
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FDA Urges Caution Following Boxed Warning Requirements on CAR T-Cell Therapies
FDA leadership notes that the overall rate of secondary T-cell cancers among patients administered CAR T-cell therapies appears to be low, even if all reported cases are assumed to be related to treatment.
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FDA Approves Expanded Indication for Dupixent to Treat Eosinophilic Esophagitis in Pediatric Patients
The FDA previously approved Dupixent in May 2022 to treat eosinophilic esophagitis in patients aged 12 years and older.
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FDA Warns Drugmakers of Additional Cancer Risks Associated with CAR T-Cell Therapy
New FDA guidelines require manufacturers to add boxed warnings to CAR T-cell therapy products.
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Reimagining Medical Education for the Digital Age
Embracing new digital-based tools is critical throughout the healthcare landscape to prepare for the rise of telemedicine as a permanent way of life.
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FDA Grants Clearance to Clinical Trial for NK CellTech’s Non-Genetically Modified Natural Killer Cells
NK010 is reportedly the first Chinese trial of its kind to be approved by the FDA.
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Gilead's Trodelvy Falls Short of Phase III Trial Primary Endpoint of Improved Overall Survival in NSCLC
The EVOKE-01 trial compared Trodelvy with docetaxel for the treatment of patients with metastatic or advanced non-small cell lung cancer who progressed on or following platinum-based chemotherapy and checkpoint inhibitor therapy.
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Weeding Out Data Inconsistencies in CDL: Q&A With Roxy McCloskey, Thought Leader at SCIEX
McCloskey discusses the steps that drug developers can take to ensure better CLD outcomes in 2024.
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Opdivo Plus Yervoy Reduces the Risk of Colorectal Cancer Disease Progression or Death by 79% Versus Chemotherapy
Opdivo plus Yervoy shows promise in treating patients with microsatellite instability-high or mismatch repair deficient metastatic colorectal cancer.
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Has Pharma Given Up on Long-Term Adherence?
Will the FDA ultimately step in and mandate a credible effort to eradicate the mindset that long-term adherence is not achievable?
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The Evolving Role of PBMs: An Interview with Bill Roth, General Manager, Managing Partner, Blue Fin Group
In an interview with Nicholas Saraceno, Bill Roth, General Manager, Managing Partner, Blue Fin Group, discusses the changing role of PBMs and recent price structure overhauls.
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Novartis' Lutathera Shows Significant Survival Benefit as First-Line Treatment for GEP-NETs
Lutathera plus long-acting release octreotide lowered the risk of disease progression or death by 72% in patients with somatostatin receptor-positive well-differentiated grade 2/3 advanced gastroenteropancreatic neuroendocrine tumors.
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Making the Case for Early-Stage Commercial Analytics
Analytics capabilities are no longer a nice-to-have, but a necessity to build and maintain a successful business and competitive edge.
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Pusan National University Announces Potential Breakthrough for Muscle Regeneration Using Nanotech
According to the university, new nanotech scaffolding can be used to support tissue growth.
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FDA Approves Balversa for Locally Advanced, Metastatic Urothelial Carcinoma
Today’s FDA approval amends a previously granted accelerated approval for Balversa (erdafitinib) to treat patients with metastatic urothelial carcinoma whose tumors harbor FGFR3 or FGFR2 alterations following prior platinum-based chemotherapy.
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Navigating Success During a Rare Disease Product Launch
Webinar Date/Time: Thu, Feb 15, 2024 11:00 AM EST
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Sun Pharma and Taro Reach Definitive Merger Agreement
Sun Pharmaceutical Industries will purchase Taro’s outstanding shares for $43 each, which will total $348 million.
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Poll Reveals Only a Small Number of Older Americans Have Used Online Direct-to-Consumer Health Services
Researchers believe low numbers in the use of direct-to-consumer healthcare services could rapidly trend up.
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FDA Approves Takeda’s HyQvia for Maintenance of Chronic Inflammatory Demyelinating Polyneuropathy
HyQvia is the only subcutaneous immune globulin infusion that can be administered once per month.
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Phesi Releases Annual Analysis of Clinical Development for 2023
New analysis for 2023 shows signs of post-pandemic recovery; breast cancer remains most studied disease area.
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Arcutis’ Zoryve Shows Progress for Individuals with Atopic, Seborrheic Dermatitis
Company displayed findings at the 2024 Winter Clinical Dermatology Conference in Hawaii demonstrating significant improvements in atopic dermatitis and seborrheic dermatitis.
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Report: Pharmaceutical Contract Manufacturing Market Expected to Hit $140 Billion by 2030
Roots Analysis report suggests increase can be attributed to the growing demand for advanced therapies and biologics.
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FDA Clears AnX Robotica’s NaviCam SB for Expanded Indications
The device can produce AI-assisted readings.
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Department of Defense Awards Emergent BioSolutions With $235.8 Million Contract for Anthrax Vaccine
The BioThrax vaccine is indicated for active immunization to prevent anthrax disease caused by Bacillus anthracis in individuals aged 18 through 65 years.
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Foundational Questions in Data Reporting, Analytics to Meet Reimbursement-Directed Marketing Goals
Measuring the relationship between a product’s reimbursement position and performance begins with gathering key data points for as many products as possible.
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Mucinex Survey Reveals Americans Only Feel Healthy For Half of Every Month
The survey is part of the brand’s new marketing campaign.
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RemeGen's Antibody-Drug Conjugate Gets FDA Fast Track Designation for Ovarian Cancer
RC88 is under evaluation for the treatment of patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, and primary peritoneal cancer.
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Dexcom Announces Preliminary and Unaudited Revenue For Fourth Quarter and Fiscal Year 2023
The company also announced that it has submitted its new glucose monitoring system to the FDA for approval.
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Will Employers Support Demand for Coverage Expansion of GLP-1 Agonists into Weight Loss?
Although medications such as Mounjaro and Zepbound have shown efficacy in helping individuals lose weight, there are not yet enough results to fully support these claims.
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S&P Global Releases Healthcare Industry Outlook for 2024
While the industry as a whole still faces challenges, there are positive trends appearing for pharmaceutical and medical device companies.
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FDA Accepts New Drug Application for Shorla Oncology’s Novel Treatment for Breast, Ovarian Cancer
SH-105 eliminates the need for powder reconstitution, which Shorla stated will bolster the novel product’s efficiency and lower the risks associated with drug preparation. The FDA has accepted Shorla Oncology’s New Drug Application (NDA) for SH-105 to treat patients with breast and ovarian cancers. The NDA was given a Prescription Drug User Fee Act action […]
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Moderna Highlights Respiratory Product Pipeline at JP Morgan Healthcare Conference
Moderna’s vaccine revenue dropped from $18.4 billion in 2022 to $6.7 billion in 2023, however the company anticipates profitability this year powered by COVID-19 vaccine sales and the launch of its mRNA-based respiratory syncytial virus vaccine. Sales of Moderna’s COVID-19 vaccine dropped from $18.4 billion in 2022 to $6.7 billion in 2023, which was ultimately […]
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