Pharmaceutical Technology

AUGUST 12, 2022

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.

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Food and Drug Administration Pharmacology Side effects Physicians 141

pharmaphorum

SEPTEMBER 16, 2022

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, side effects do happen.

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pharmaphorum

JANUARY 6, 2023

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

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Prescription Manufacturing Patients Side effects 105

European Pharmaceutical Review

JUNE 12, 2024

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.

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pharmaphorum

JUNE 24, 2022

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.

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European Pharmaceutical Review

MAY 23, 2024

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.

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Food and Drug Administration Food Medical Medicine 110

pharmaphorum

JULY 13, 2022

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.

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European Pharmaceutical Review

OCTOBER 19, 2023

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.

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Food and Drug Administration Manufacturing Side effects Doctors 105

Pharmaceutical Technology

NOVEMBER 1, 2022

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 side effects of different therapies.

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Pharmaceutical Technology

JULY 29, 2022

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.

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PM360

OCTOBER 22, 2024

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).

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pharmaphorum

SEPTEMBER 22, 2022

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.

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Pharmaceutical Technology

SEPTEMBER 23, 2022

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 side effects including loss of appetite, nausea, and ototoxicity (hearing loss).

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European Pharmaceutical Review

AUGUST 14, 2023

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 side effects of the available drugs, according to Dalsgaard. C21 was also trialled in a study for patients with COVID-19.

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Pharma Side effects Patients Manufacturing 98

pharmaphorum

SEPTEMBER 8, 2022

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 side effects which can impact patients’ lives. billion acquisition of Endocyte in 2018 , with estimations that sales could reach $600 million in this first indication alone.

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Pharmaceutical Technology

AUGUST 17, 2022

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

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Pharmaceutical Technology

NOVEMBER 3, 2022

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 side effects usually seen with antipsychotic agents.

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Food and Drug Administration Side effects Food Patients 52

European Pharmaceutical Review

DECEMBER 14, 2023

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

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Pharmaceutical Technology

SEPTEMBER 26, 2022

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.

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Clarivate

SEPTEMBER 25, 2024

A ‘magic bullet’ medicine that can cure a disease quickly and completely, [1] without deleterious side effects. [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

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Medicine Side effects Patients Pharmaceutical 59

Pharmaceutical Technology

OCTOBER 13, 2022

Most currently available therapeutic options for endometriosis often have a diminished efficacy over time and result in negative side effects such as menopausal-like side effects and bone mineral density (BMD) loss.

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Food and Drug Administration Pharma Side effects FDA 52

PM360

AUGUST 9, 2022

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.

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Education Side effects Physicians Patients 59

European Pharmaceutical Review

AUGUST 24, 2022

The ultimate goal of the ADC concept is to maximise the potency of treatment and reduce unwanted side effects 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.

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Engineering Side effects Marketing Patients 104

pharmaphorum

JULY 11, 2022

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 side effects. Sanofi acquired the drug when it bought Bioverativ in 2018 for $11.6

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European Pharmaceutical Review

AUGUST 15, 2024

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

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Pharmaceutical Technology

JANUARY 22, 2023

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.

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Pharmaceutical Technology

NOVEMBER 30, 2022

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 side effects. The same can be said for the US. of adults were overweight, 42.4%

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Medical Manufacturing Insurance Side effects 105

Pharmaceutical Technology

NOVEMBER 30, 2022

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 side effects. The same can be said for the US. of adults were overweight, 42.4%

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Medical Manufacturing Insurance Side effects 98

Pharmaceutical Technology

MARCH 24, 2023

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.

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Pharma Side effects Marketing Biopharma 64

World of DTC Marketing

FEBRUARY 23, 2021

How long do you believe it will be before the media once again runs stories about drug prices or drug side effects? 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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Pharmaceutical Technology

MAY 31, 2023

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.

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