CLINICAL ROLE -
Kennedy Ferruggia is an assistant editor at Pharmacy Times®. She graduated from The College of New Jersey in 2023 in journalism and marketing. Prior to this position, she worked as a pharmacy associate for community pharmacies.
Study Finds High Prevalence of Vitamin and Mineral Deficiency in Type 2 Diabetes
Investigators found that 60% of individuals with type 2 diabetes are vitamin D deficient.
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Expert: FDA Approves Tocilizumab-Anoh as a Biosimilar to Actemra
Tocilizumab-anoh is expected to increase competition, improve patient access, and deliver cost savings in the treatment of various inflammatory conditions.
Oral Antiviral Candidate Shows Promise for Respiratory Syncytial Virus Treatment
S-337395 demonstrated an 88.4% reduction in viral load and had a statistically significant improvement in clinical symptoms scores.
Study: Radiotherapeutic Agent for GEP-NETs Demonstrates Positive Results
Lu-edotreotide (ITM-11; ITM) met its primary endpoint of prolonging progression-free survival (PFS).
Belzutifan Receives FDA Priority Review for Advanced Pheochromocytoma and Paraganglioma
The supplemental new drug application is based on objective response rate and duration of response results from a phase 2 study that assessed the efficacy and safety of belzutifan.
FDA Accepts Review of Biologics License Application for AVT05, a Biosimilar Candidate for Golimumab
This marks the first US biologic license application filing acceptance for a biosimilar candidate to golimumab.
CD5 CAR-T Cell Therapy Receives FDA Orphan Drug Designation for T-Cell Lymphoma
MB-105 is a first-in-class CD5-targeted chimeric antigen receptor (CAR) T-cell therapy for the treatment of relapsed or refractory CD5-positive T-cell lymphoma.
Pembrolizumab Plus Lenvatinib Combination Shows Mixed Results in Gastroesophageal Cancer
The trial meets one of the study’s dual primary endpoints of progression-free survival, but did not meet its other primary endpoint of overall survival.
A Single Sample Sexually Transmitted Infection System Receives FDA Clearance With CLIA Waiver
The cobas liat system is a closed system that aims to reduce contamination risks and enhances the reliability of results at the point of care.
The Role of Antivirals in Managing RSV Infections
Antiviral treatments for respiratory viruses such as respiratory syncytial virus (RSV) are crucial, especially with the rise of the "triple-demic."
Study: Bile Acid Supplement Shows Promise for Liver Cancer
Boosting ursodeoxycholic acid (UDCA) levels through dietary supplementation was shown to control tumor growth in mice with liver cancer.
Study: Biosimilar Efficacy and Safety in Pediatric Inflammatory Bowel Disease
Biosimilar use is not linked to an increased risk of treatment failure among pediatric patients with inflammatory bowel disease (IBD).
Observational Study Aims to Assess RSV Incidence and Impact in Older Adults
Point-of-care testing implementation could provide valuable data on community respiratory syncytial virus incidence and enhance sentinel surveillance efforts.
DYNE-101 Receives FDA Fast Track Designation to Treat Myotonic Dystrophy
The fast-track designation follows the FDA orphan drug designation that was granted for DYNE-101 in September 2023 for the same treatment population.
Study: Biotin Could Protect Against Manganese-Induced Parkinson Disease
Biotin supplementation could mitigate manganese-induced damage caused by manganese deficiency and excessive exposure.
FDA Gives Priority Review to Vusolimogene Oderparepvec for Melanoma
Vusolimogene oderparepvec in combination with nivolumab is being assessed to treat individuals with unresectable or metastatic stage IIIb-IV cutaneous melanoma.
SEL-212 Shows Promise in Treating Chronic Refractory Gout with High Response Rates
Pharmacists play a significant role in managing gout by educating patients about the disease and ensuring proper medication adherence to urate-lowering therapy.
FDA Targets Nicotine to Reduce Lung Cancer and Other Tobacco-Related Diseases
The FDA proposes to cap the nicotine level at 0.7 mg per gram of tobacco in cigarettes and certain other combusted tobacco products.
FDA Approves Axatilimab-csfr 9 mg and 22 mg Vial Sizes for cGVHD
The current approved dose of axatilimab-csfr is 0.3 mg/kg up to a maximum dose of 35 mg and will be administered as an intravenous infusion over 30 minutes every 2 weeks.
Survey Shows Gaps in Consumer Awareness of Pharmacist Services
Rite Aid survey highlights underutilized role of pharmacists in health care, with 62% of respondents viewing their pharmacists as a crucial part of their health and wellness care team.
mRESVIA RSV Vaccine Is a Key Area to Watch for Community Pharmacy in 2025
mRNA-1345 (mRESVIA; Moderna) has the potential to significantly transform the RSV disease state in 2025, according to data analysts.
Dietary Supplement Age Restrictions: Concerns for Consumers, Retailers, and Public Health
The proposed age restrictions on dietary supplements would limit consumer access to safe products.
FDA Grants Breakthrough Therapy Designation to GSK’227 to Treat Osteosarcoma
The designation was supported by data from the phase 2, open-label, randomized, multi-center ARTEMIS-002 clinical trial, which assessed the safety and efficacy of GSK’227.
Phase 2 Study Evaluates Serplulimab Plus HLX04 as First-Line Treatment for Advanced Hepatocellular Carcinoma
Serplulimab plus HLX04 demonstrates a favorable safety profile in patients with advanced hepatocellular carcinoma.
Posdinemab Receives FDA Fast Track Designation for Treatment of Alzheimer Disease
As an investigational monoclonal antibody, posdinemab targets the mid-domain of AD-specific phosphorylated tau.
Rise in RSV Infections Is Associated With a Decrease in Vaccine Hesitancy
Approximately 61% of individuals said respiratory syncytial virus (RSV vaccination for adults 60 years and older is effective.
Avutometinib Plus Defactinib Moves One Step Closer to Approval for Treatment of Ovarian Cancer
If approved, the combination of avutometinib with defactinib could be the first FDA-approved treatment option for low-grade serous ovarian cancer.
Study Misinterprets Heavy Metal Levels in Prenatal Vitamins, Causing Unnecessary Concern
The inaccurate claim that these products pose a heavy metal risk is potentially detrimental, as it could discourage pregnant women from using vital prenatal supplements.
Study Suggests Weakened RSV Vaccine Response in Immunocompromised Individuals
Immunocompromised older adults developed fewer antibodies against RSV following vaccination compared with immunocompetent individuals.
Study: Shingles Could Significantly Increase Risk of Dementia and Parkinson Disease
Researchers recommend early vaccination against herpes zoster to mitigate the risks.