Dupilumab Is Safe and Effective for Long-term Use in Kids
Drug Topics
SEPTEMBER 15, 2022
Improvements in atopic dermatitis symptoms were seen in children taking dupilumab, with minimal adverse events.
Drug Topics
SEPTEMBER 15, 2022
Improvements in atopic dermatitis symptoms were seen in children taking dupilumab, with minimal adverse events.
PharmaVoice
SEPTEMBER 15, 2022
Sonara Health’s inexpensive, specially engineered label and web app allow for at-home, digitally supervised dosing of high-cost or high-risks drugs.
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Drug Topics
SEPTEMBER 15, 2022
William J. Muller, MD, PhD, discusses COVID-19 vaccinations for children of all ages and describes what is on the horizon for RSV.
STAT
SEPTEMBER 15, 2022
Artificial intelligence is a transformative tool in the workplace — except when it isn’t. For top managers, state-of-the art AI tools are a no-brainer: in theory, they increase revenues, decrease costs, and improve the quality of products and services. But in the wild, it’s often just the opposite for frontline employees who actually need to integrate these tools into their daily work.
Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.
The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven
Pharmacy Times
SEPTEMBER 15, 2022
Deucravacitinib is a selective, allosteric tyrosine kinase 2 (TYK2) inhibitor, which is a member of the Janus kinase (JAK) family.
pharmaphorum
SEPTEMBER 15, 2022
The competition authorities in Switzerland said this morning they have carried out a raid on a pharma company – now confirmed to be Novartis – as part of an investigation into a “possible unlawful use of a patent to reduce competitive pressure.” The Swiss Competition Commission (COMCO) arrived unexpectedly at Novartis at dawn on Tuesday morning, to gather information on an unidentified dermatology drug, as part of a wider investigation into the drugmaker by the European Commission.
Pharmacy Technician Pulse brings together the best content for pharmacy technicians from the widest variety of industry thought leaders.
Drug Store News
SEPTEMBER 15, 2022
According to a survey by Reach 3 Insights, 80% of Americans say that rising prices have driven them to purchase more store-brand products.
Pharmacy Times
SEPTEMBER 15, 2022
Researchers have identified hydroquinine as a potential treatment against drug-resistant bacteria, which can cause infections with a 70% mortality rate.
Pharmaceutical Technology
SEPTEMBER 15, 2022
Last year was a positive year for biopharmaceutical companies, particularly those with Covid-19 vaccines. The top 13 players reported more than 10% revenue growth, with BioNTech (3,834.4%), Moderna (2,199.1%), Pfizer (95.2%) and Regeneron Pharmaceuticals (89.1%) reporting a more than 80% year-on-year (YoY) revenue growth from 2020 to 2021, according to GlobalData’s Pharma Intelligence Centre Companies Database.
Pharmacy Times
SEPTEMBER 15, 2022
Alopecia areata is an autoimmune disease with an underlying immuno-inflammatory pathogenesis.
Speaker: Chris Antypas and Josh Halladay
Access to limited distribution drugs and payer contracts are key to pharmacy expansion. But how do you prepare your operations to take the next step? Meaningful data: Collect and share clinical data regarding outcomes, utilization, and more Reporting: Limited distribution models require efficient tracking and reporting systems Workflows: Align workflows with specific pharma and payer contractual requirements For in-depth, expert insights on pharmacy expansion, watch this webinar from Inovalon.
Pharma Tutor
SEPTEMBER 15, 2022
AN APPROACH TO THE HAIR FALL & HAIR GROWTH MANAGEMENT. About Authors Avdesh Thassu. MPharm (Nat. Chem.); MBA(Mkt.). Associate Vice President. Global Regulatory Affairs, Emami Limited, 7044455199. athassu@hotmail.com. Chandra Mohan Nandi. MSc. (Organic Chem.). Deputy Manager, Global Regulatory Affairs, Emami Limited, 9051706947 chandramohannandi@yahoo.in. admin.
pharmaphorum
SEPTEMBER 15, 2022
The potential for technology to transform the way we deliver healthcare is nothing new. We’ve been discussing it for some years now and are starting to see more widespread adoption, particularly post-pandemic. But the area where I believe technology can have the greatest impact – and where there is still plenty of work to do – is women’s health. Today, women spend around a quarter of their lives in poor health or disability, compared with one fifth for men.
STAT
SEPTEMBER 15, 2022
The Swiss Competition Commission has begun an investigation into Novartis over the possible unlawful use of a patent to block competitors for some of its medicines, the latest instance in which European authorities have probed drug companies for antitrust infractions. Earlier this week, the Swiss agency conducted a dawn raid on Novartis headquarters in Basel, Switzerland, seeking information about efforts the company allegedly made to protect a drug for an unspecified skin treatment.
European Pharmaceutical Review
SEPTEMBER 15, 2022
Investing close to €300 million, Takeda plans to construct a new state-of-the-art production facility for plasma-derived therapies and a net-zero carbon emissions warehouse in Lessines, Belgium – the largest investment Takeda has ever made in the country. The investment is part of the company’s global effort to implement the most innovative technologies and most sustainable processes at its manufacturing sites.
Speaker: Dr. Ben Locwin - Biopharmaceutical Executive & Healthcare Futurist
What will the future hold for clinical research? A recent draft from the FDA provides valuable insight. In "Optimizing the Dosage of Human Prescription Drugs and Biological Products for the Treatment of Oncologic Diseases," the FDA notes that "targeted therapies demonstrate different dose-response relationships compared to cytotoxic chemotherapy, such that doses below the Maximum Tolerated Dose (MTD) may have similar efficacy to the MTD but with fewer toxicities.
STAT
SEPTEMBER 15, 2022
WASHINGTON — A Democratic House lawmaker with oversight authority is calling for an investigation into the largest for-profit hospital chain in the country, HCA Healthcare. Rep. Bill Pascrell (D-N.J.), the chair of the House Ways and Means Committee’s subcommittee on oversight, this week asked the Department of Health and Human Services to investigate whether HCA is improperly admitting emergency department patients to the hospital when they don’t need inpatient care.
European Pharmaceutical Review
SEPTEMBER 15, 2022
According to Novartis, Kisqali ® (ribociclib) plus endocrine therapy in the first-line setting added nearly a year of additional overall survival (OS) benefit in a subgroup of patients with aggressive forms of hormone receptor-positive, human epidermal growth factor receptor-2 negative (HR+/HER2-) advanced breast cancer (aBC). The pooled exploratory analysis from the MONALEESA Phase III programme revealed that patients with visceral metastases, including liver metastases and multiple metastatic
STAT
SEPTEMBER 15, 2022
A host of health tech startups and companies are advertising their apps and platforms as key solutions to improving diversity in clinical trials, promising to help researchers improve their outreach, enrollment, and retention — what one researcher calls a “modern-day gold rush.” The Power platform focuses on breaking down medical jargon and helping users connect with trial sponsors nearby.
Drug Store News
SEPTEMBER 15, 2022
The beauty category, most notably the skin care space, has seen a massive resurgence in the demand for environmentally friendly, clean, vegan and cruelty-free products.
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STAT
SEPTEMBER 15, 2022
You’re reading the web edition of STAT Health Tech, our guide to how tech is transforming the life sciences. Sign up to get this newsletter delivered in your inbox every Tuesday and Thursday.
ISPE
SEPTEMBER 15, 2022
Annex 1 Implementation Strategies. Trudy Patterson. Thu, 09/15/2022 - 13:50. iSpeak Blog. iSpeak. Annex 1 Implementation Strategies. Thomas Zimmer, PhD. 15 September 2022. Annex 1 of the EC GMP Guide " Manufacture of Sterile Medicinal Products " has a long history. First published in 1989, there have been a total of 5 adaptations in 1996, 2003, 2005, 2007 and 2009, but no complete revision.
STAT
SEPTEMBER 15, 2022
Rise and shine, everyone, another busy day is on the way. This morning is getting off to a fabulous start, though, as a delightfully cool breeze and warm sun are enveloping the subdued Pharmalot campus, where the official mascot is snoozing nearby. As always, we are quaffing some cups of stimulation — chocolate raspberry is our choice du jour — and assembling some tidbits for your pleasure.
Drug Store News
SEPTEMBER 15, 2022
Utilizing Amazon Customer Engagement’s Tailored Audiences, sellers can now increase their email marketing reach and build brand loyalty, the company said.
Pharmacy Times
SEPTEMBER 15, 2022
Services such as managing/updating patient programs and working with non-profits can go a long way in healthcare education for patients.
Drug Store News
SEPTEMBER 15, 2022
Dr. Scholl’s is working with former head football coach and analyst Rex Ryan and surgeon Brad Schaeffer of TLC’s “My Feet Are Killing Me” on the launch of its Instant Cool Athlete’s Foot solutions.
Pharmacy Times
SEPTEMBER 15, 2022
Part A results from the 2-part LILAC study show that the therapy significantly reduced disease activity based on active joint count in individuals compared with the placebo.
Drug Store News
SEPTEMBER 15, 2022
Generic Faslodex is used to treat advanced-stage, hormone receptor-positive, HER2-negative breast cancer.
Pharmacy Times
SEPTEMBER 15, 2022
Panelists discuss pharmacist involvement in effective management, including disease burden and quality of life.
Outsourcing Pharma
SEPTEMBER 15, 2022
Faeth Therapeutics aims to remove roadblocks to âanyone other than the wealthiest patientsâ through remote trial partnership.
pharmaphorum
SEPTEMBER 15, 2022
Pfizer’s close-fought contest with GSK to bring a next-generation meningitis vaccine to market has entered the final rounds, with the former ahead on points following the readout of a pivotal phase 3 clinical trial. Both companies are developing MenABCWY vaccines that cover all five meningococcal strains in one go as an alternative to separate vaccinations, in the hope of simplifying immunisation schedules and reducing the number of injections needed, as well as potentially enhancing uptak
Outsourcing Pharma
SEPTEMBER 15, 2022
Australian CRO Avance Clinical has expanded in North America by acquiring C3 Research Associates, positioning it to continue supporting sponsors as they move into later-phase studies that need US sites.
PharmExec
SEPTEMBER 15, 2022
In episode 117, Helen Sabzevari, CEO of Precigen, discusses her drive to study science as a Persian-born woman, the opportunities she’s had to research immunology, and how she’s now developing next-generation CAR-T treatments for cancer, in addition to other therapies.
Pharmaceutical Technology
SEPTEMBER 15, 2022
Research by GlobalData (Contract Small Molecule API Manufacturing Industry by the Numbers – 2021 Edition) shows that containment facilities are in high demand as the use of cytotoxic drugs continues to grow. The same research also shows that all the top small molecule API contract manufacturing organisations (CMOs) increased the number of containment facilities they owned between 2019 and 2021, while at the same time, many companies decreased non-containment, small molecule manufacturing.
pharmaphorum
SEPTEMBER 15, 2022
The Clinical Data Interchange Standards Consortium (CDISC) is dedicated to the improvement of medical research through data standardization. CDISC has produced a suite of standards that should be used to standardize content from planning and data collection through to data analysis and reporting. The United States Food and Drug Administration (FDA) now requires studies to be submitted in this standardized format.
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