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Yet the media has led with “diabetes drug leads to major weight loss” Will doctors inform patients? Wegovy’s most common sideeffects were gastrointestinal problems, including nausea, diarrhea, and vomiting, which 80% of patients reported, according to USA Today.
Using 2018 National Health Interview Survey (NHIS) data, we provide estimates of the prevalence of single and multiple chronic conditions among US adults. Our healthcare system is designed to treat health conditions, not patients. The post Quality of life in patients with chronic health conditions. That needs to change.
billion in 2018, and is expected to grow at a CAGR of 7.20% to reach $86.01 Jazz Pharmaceuticals has introduced a new prescription medication for patients with sleep apnea/narcolepsy that “helped adults get up to 9 hours of improved wakefulness in clinical studies at 12 weeks” and they’re using a flying pig on their DTC.
The Medicines and Healthcare products Regulatory Agency (MHRA) aims to launch a pilot genetic biobank that will gather patient data to associate drug-related adverse events to their genetic makeup. Sideeffects due to drugs are responsible for one in every 16 hospital admissions in the UK, based on the announcement.
Cancer-support programs provide vital assistance to patients and their caregivers as they face one of the toughest times of their lives. Yet while patients are interested in these programs, new survey data suggests they aren’t taking advantage of them. We’re committed to serving the entire patient community.”
Amgen CEO Bob Bradway racked up a 2018 pay package of $18.6 Food and Drug Administration (FDA) is meant to help patients and warn of potential drug sideeffects but a Vice report indicates something more. She later learned that her manager’s boss was behind the termination because she feared for her own job.
The availability of oral chemotherapy treatments would provide stomach cancer patients with the option of more efficacious drugs with improved tolerability in a more convenient dosage format” The poor clinical outcomes of stomach cancer make it a key target for drug development. New hope for stomach cancer patients.
The FDA’s breakthrough device programme is for medical devices or device-led combination products that provide more effective treatment or diagnosis of diseases. The aim of the programme is to expedite the development, assessment and review of medical devices in order to provide timely access to patients and healthcare providers.
Atopic dermatitis (AD) is a highly prevalent chronic dermatological disease, with symptoms which include itching, dry skin, severe pain, and inflammation – all of which create considerable stress in the daily lives of patients and often negatively affect their day-to-day and long-term well-being. However, sideeffects do happen.
In 2023, expect manufacturers to further shift their focus away from acquiring new patient prescriptions to retaining existing customers. Ensuring patient access. Retaining business begins with patient access. Preventing patient drop-off. in 1979 to 2.8%in
Since 2018, biotech company Mikrobiomik has been researching, development and producing innovative biological medicines based on the human microbiome. The study included 92 adult patients with confirmed CDI. After treatment, patients were followed up at intervals of 72 hours, three weeks, eight weeks, three months and six months.
If treatment is prompt and effective, patients can live a normal lifespan, but left untreated the disease can be fatal. Some patients do not respond adequately to current treatment like penicillamine or trientine and zinc therapy, however, and continue to experience symptoms.
The best reps focus on patients, not prescriptions. These reps are engaged in the community around their disease state, focused on the health and needs of patients over their product. They are focused on patient outcomes, not just patient onboarding. Thats how I get information to help patients, one HCP said.
1 Particularly, CAR-T cell therapy, which uses a patient’s T-cells to fight cancer by altering them so they can find and destroy cancer cells, has emerged as a valuable option for many patients. 2 With this new indication, more patients will be able to access this innovative treatment.
Verve Therapeutics has started dosing patients in a phase 1b trial of its in vivo gene-editing drug for high cholesterol, designed to permanently switch off the PCSK9 gene with a one-shot treatment. 2018: @VerveTx founded with concept of one-time Rx to lower LDL as low as possible for as long as possible. . Today: we are announcing.
The development of novel radiotherapeutics ushered in a new era in targeted treatment 1 for cancer, with two separate radiotherapeutic approvals in Europe and the US, in 2018 and 2022. These diagnostics are also paired with therapeutics and act as an imaging biomarker to identify patients who may benefit from the paired therapies.
In Estonia, every patient who visits a doctor immediately has their own personal e-Health record updated with new information, which can be referred to in future appointments. intervention) was the “cause” of an effect. These studies are often done to understand the sideeffects of different therapies.
While the prevalence was 1 in 150 children in 2000, it reached the rate of 1 in 44 in 2018, in the US, according to the Centers for Disease Control and Prevention. A nasal spray might a preferred option for some patients, especially if it acts faster than an injection, which often takes effect after the agitation period ends, he says.
In the pharmaceutical industry, patient support programs (PSPs) and brand teams often work in silos, despite their shared goal of helping patients achieve a certain health outcome. Pharma brands work diligently to win the trust of key stakeholders—namely patients, caregivers, and healthcare providers (HCPs).
California biotech Calibr and partner AbbVie have reported the first clinical data on a new CAR-T technology, which uses “switchable” cells that aim to eliminate the life-threatening side-effects that can occur with this type of immunotherapy.
In 2022, the FDA approved only 37 new medicines, an underwhelming number compared to 98 in 2018. However, while only around 34% of the approvals in 2018 were for orphan drugs, 54% new approvals in 2022 were for drugs to treat rare diseases. The NSAA measures functional motor abilities in DMD patients.
The recent FDA approval of Fennec Pharmaceuticals’ drug PEDMARK (sodium thiosulfate injection) marks a significant advance for cancer treatment-associated hearing loss therapies, amidst a bid to improve quality of life for cancer patients. Cisplatin has multiple sideeffects including loss of appetite, nausea, and ototoxicity (hearing loss).
This data, together with a favourable safety profile, make C21 a potential game-changer for IPF patients, particularly those who are currently not treated due to the sideeffects of the available drugs, according to Dalsgaard. C21 was also trialled in a study for patients with COVID-19.
The problem with this form of treatment is that it is not targeted and, as a result, there are a number of short- and long-term sideeffects which can impact patients’ lives. billion acquisition of Endocyte in 2018 , with estimations that sales could reach $600 million in this first indication alone.
The funding will be used for the Phase III clinical trial and potential marketing of the investigational compound, ecopipam, for treating Tourette syndrome patients. Additionally, trial subjects did not have adverse movement or metabolic sideeffects usually seen with antipsychotic agents.
cases per 100,000 people in 2018. “In In a separate Phase II VLA15-221 study, which looked at adult and pediatric patients, the vaccine had stronger immunogenicity in children than in adults. In the UK, the mean annual incidence of Lyme disease grew from 0.38 cases per 100,000 people between 1997 and 2000 to a peak of 2.77
They also include many of the common “exclusions” in RCTs, such as pregnant women, children, the elderly and patients on multiple medications. million patients were registered with GP practices in England, which hold health information about each person “from the cradle to the grave”. 2018; 8(1). As of October 2023, 62.93
The UK National Institute for Health and Care Excellence (NICE) has granted approval for Pfizer ’s palbociclib (Ibrance) in combination with anti-cancer therapy, fulvestrant, to treat advanced breast cancer patients. In addition to palbociclib, NICE has granted approval for 15 other therapies for breast cancer since 2018.
A ‘magic bullet’ medicine that can cure a disease quickly and completely, [1] without deleterious sideeffects. [2] 3 Patients required many injections over a long time period, and problems also arose from the galenic preparation of arsphenamide, which was insoluble in water.3
Most currently available therapeutic options for endometriosis often have a diminished efficacy over time and result in negative sideeffects such as menopausal-like sideeffects and bone mineral density (BMD) loss.
Medication non-adherence has a staggering impact on the industry’s ability to serve patient well-being and achieve growth. A patient is diagnosed and prescribed a treatment to correct or mitigate a condition. However, most patients have very little time with their physician to learn all aspects of their prescribed medication.
The ultimate goal of the ADC concept is to maximise the potency of treatment and reduce unwanted sideeffects on healthy tissues. This excitement will surely propel a next generation of ADCs to patients in cancer indications with a high medical need that are currently not well served with standard of care.
A 2017–2018 National Health and Nutrition Examination Survey (NHANES), showed that 30.7% In the past, obesity medications were often dismissed due to insufficient efficacy data and the fact that they were associated with a high occurrence of sideeffects. The same can be said for the US. of adults were overweight, 42.4%
The company had been eyeing a possible regulatory filing for fitusiran this year, but has now set back the timeline – possibly until 2024 – while it gathers data on the revised dosing schedule, in the hope of maintaining efficacy with fewer clotting sideeffects. Sanofi acquired the drug when it bought Bioverativ in 2018 for $11.6
A 2017–2018 National Health and Nutrition Examination Survey (NHANES), showed that 30.7% In the past, obesity medications were often dismissed due to insufficient efficacy data and the fact that they were associated with a high occurrence of sideeffects. The same can be said for the US. of adults were overweight, 42.4%
BTKis, oral drugs given as continuous monotherapy, have revolutionised the treatment of CLL, with the first generation BTKi ibrutinib receiving European Medicines Agency (EMA) approval in 2014; however, side-effects (such as cardiovascular toxicities 2 ) have limited its suitability. for all-comers; HR=0.52
The proposed “ Patient Medication Information ” guide would be an FDA-approved, one-page document that includes the necessary information for patients to understand the drug product and how to use it. Due to this, patients often take their medications incorrectly, or stop taking them entirely, which causes further harm.
New Developments for TB In a recent Phase I clinical trial (NCT03722472), researchers have been able to test the first thermostable TB vaccine in patients. In this trial, patients were given a thermostable version of the vaccine or a non-thermostable vaccine in two treatment regimens.
How long do you believe it will be before the media once again runs stories about drug prices or drug sideeffects? The increase followed total Humira price hikes of 19 percent during 2017 and 2018, according to a survey by the nonprofit Institute for Clinical and Economic Review, which deemed the increases unjustified.
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