Pharmaceutical Technology

MAY 2, 2023

There are more than 20 marketed ICIs with approvals across a very wide spectrum of solid tumour indications. While initially only approved for metastatic disease, ICIs have now moved into earlier disease settings, reducing the risk of disease progression and relapse. Cost-related unmet needs also scored highly.

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pharmaphorum

MAY 10, 2022

The two partners have also requested a priority review for the Biologics License Application (BLA) for lecanemab, which if granted by the FDA could result in an approval before the end of the year. The post Exit Aduhelm, enter lecanemab. Biogen and Eisai have another go appeared first on.

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pharmaphorum

APRIL 27, 2022

Drugs given the designation are hastened through the development process by the FDA, which can grant them a faster six-month review. The post Enhertu gets breakthrough tag in HER2-low breast cancer appeared first on.

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Chemotherapy FDA 57

Pharmaceutical Technology

APRIL 13, 2023

Two gene therapies up for approval this year for sickle cell disease could be cost effective in some cases at a $2 million price point, based on a draft evidence report published by the Institute for Clinical and Economic Review (ICER). If approved, exa-cel would be the first FDA-approved gene therapy based on CRISPR editing.

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FDA 59

The Checkup by Singlecare

DECEMBER 5, 2023

The #ozempic tag on TikTok has amassed over 1 billion views to date. Although weight loss is a side effect of Ozempic, it isn’t approved as a weight loss drug. It can help trigger a feeling of fullness after a meal and slow the digestion process. Ozempic became one of the most talked about drugs in 2023.

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Insurance Prescription Filling FDA Dosage 105

Viseven

JUNE 23, 2022

In a few words, you can adapt it, but the core always stays the same, as you have a pre-approved solution. Thanks to the unification, there’s no need to look out for a branding design code or create content from scratch — go on with pre-approved modular content, interpreting it to suit your needs. How to calculate cost efficiency?

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Communication 52

pharmaphorum

DECEMBER 23, 2022

Add to this the considerable cost of these medications – the first approved CAR-T, Novartis’ Kymriah (tisagenlecleucel), had a U.S. price tag of $475,000 when it was first launched in 2017 – and it becomes apparent that these may not be desirable treatment options for every patient and in every setting.

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Pharmaceutical Technology

APRIL 5, 2023

More than a decade after the first patient was treated with a CAR-T therapy, six therapies relying on the same principles have been approved by the US Food and Drug Administration (FDA) and marketed to thousands of patients. It will be six years since the US FDA approval of Kymriah in August this year.

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FDA Immunization 59

pharmaphorum

JANUARY 31, 2023

With the recent rapid rollout of Covid-19 vaccines, many people have raised questions about whether adequate research was conducted on these vaccines before approval. What people did not understand was that “fast tracking” approval does not limit the rigorous process involved in ensuring that a medication or vaccine is safe for market use.

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Pharmaceutical Companies Pharmaceutical Companies Vaccines Communication 52

pharmaphorum

MAY 24, 2021

Robb DeFilippis, managing director, life sciences, for end-to-end global creative production and sourcing partner Tag in the Americas agrees. Modular content, or ‘atomic’ design as it’s sometimes known, is the process of creating modules of content to be assembled in any way the user requires. Robb DeFilippis. ” Robb DeFilippis.

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Communication Packaging Pharmaceutical Companies Pharmaceutical Companies 101

pharmaphorum

DECEMBER 2, 2020

They developed a deep tank fermentation process, the principles of which would later be applied to the production of penicillin. For all the latest Pfizer news follow pharmaphorum’s Pfizer tag. Pfizer initiated its first major internationalisation at this stage, moving into nine new countries in 1951.

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Compounding Vaccines Pharmaceutical Companies Pharmaceutical Companies 127

pharmaphorum

NOVEMBER 16, 2022

It is no secret that the drug development process for the pharmaceutical industry has undergone a major transition in the last few decades. Previously, the discovery of small molecule treatments had been the priority, with their development and manufacturing process being an established formula. However, with a price tag of €1.58

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The Checkup by Singlecare

MARCH 21, 2023

Belbuca (buprenorphine) Belbuca is a buccal film of the active ingredient, buprenorphine , that is approved for chronic pain. Belbuca is a good alternative to opioid treatment that needs to be taken around the clock, but it may come with a hefty price tag. With that said, tapering should be an individualized process.

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Dosage Controlled Substances Labelling Packaging 52

Pharmaceutical Technology

JUNE 21, 2023

CSL announced the first patient with haemophilia B has been treated with its recently approved gene therapy Hemgenix (etranacogene dezaparvovec). Hemgenix is the first and only gene therapy approved for haemophilia B. Despite the limited market, the price tags of haemophilia make it potentially lucrative.

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FDA 98

Viseven

SEPTEMBER 14, 2023

The pharma sector now reconsiders its procurement process for improved efficiency, resilience, and cost optimization. Climate change is another factor, potentially disrupting supplies and contributing to hefty price tags. Discover the innovative approaches that pharma brands employ to effectively address challenges and drive progress.

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Packaging Pharmaceutical Companies Pharmaceutical Companies Pharmacy Procurement 52

Roots Analysis

SEPTEMBER 13, 2023

Conjugation is the process of formation of a single, stable hybrid, wherein one of the entities is a molecule, such as protein, antibody, peptide and small molecule. These conjugates lead to elucidation of complex biological processes via signal amplification and high biological specificity.

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Labelling 40

pharmaphorum

SEPTEMBER 30, 2022

Over the years, pharmaceutical companies seeking product approvals have submitted increasingly vast amounts of information to regulatory agencies. Regulatory agencies are embracing standardized review processes (such as the FDA’s KASA project) that benefit from direct data collection and incorporate review metrics. Making it happen.

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Pharmaceutical Technology

JANUARY 27, 2023

In 2019, Cablivi became the first FDA-approved , nanobody-based medicine for acquired thrombotic thrombocytopenic purpura (aTTP), an ultra-orphan condition that causes blood clots in small blood vessels around the body. Furthermore, he said extracting data to validate the criteria for a warranty reimbursement could be an onerous process.

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Documentation Immunization Pharmaceutical Companies Pharmaceutical Companies 52

The Checkup by Singlecare

MARCH 7, 2024

It was approved by the Food and Drug Administration (FDA) in 2017 for treating Type 2 diabetes. Ozempic cost Unfortunately, like many new drugs, Ozempic comes with a hefty price tag. Ozempic (semaglutide) is a weekly injectable drug that lowers blood sugar levels. Vet each pharmacy carefully This is arguably the most important step.

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Health and Personal Care Stores Insurance Packaging Insurance Coverage 52

pharmaphorum

DECEMBER 2, 2020

The New York-based firm has requested approval for the combination of its anti-CD20 antibody ublituximab and umralisib, an oral drug that inhibits PI3K-delta and CK-1 epsilon. The FDA had already granted fast-track designation to the combination therapy, allowing extra help during the development process on the basis of earlier clinical data.

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FDA Chemotherapy 52

pharmaphorum

FEBRUARY 26, 2021

J&J has been bullish in both its insistence that the claims are inflated or false and that it can easily deal with the lawsuits, but the company has both won and lost existing cases, with many still caught up in appeals processes, and it remains to be seen how the balance will eventually play out. Acquisitions post-Janssen.

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Vaccines Labelling Communication 125

European Pharmaceutical Review

NOVEMBER 10, 2022

There are three primary reasons for the failure of complex medicines: Biodistribution – due to physiological factors, complex formulations often preferentially target the liver, and as a result, many of the clinically approved complex medicines target liver disease. Physical characterisation.

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European Pharmaceutical Review

DECEMBER 27, 2023

Currently CAR T-cell therapy is approved for three indications: acute lymphoblastic leukaemia (ALL), non-hodgkin lymphoma (NHL), and multiple myeloma (MM) – and the strongest correlation between CAR T-cell efficacy and persistence has been demonstrated in ALL. This is in addition to its considerable price tag.

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Adverse Reactions Immunization Medical Schools Chemotherapy 92

The Social Pharmacist

AUGUST 23, 2022

Then, you need to label each self-created link with “no follow” tags. It includes content, keywords, meta tags, and backlinks. Each subtle indication functions as the person or company linking to your site approve of your blog or business. Backlinks tell Google that others approve of your content. Keyword: Backlinks.

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Labelling 52

The Social Pharmacist

AUGUST 23, 2022

Then, you need to label each self-created link with “no follow” tags. It includes content, keywords, meta tags, and backlinks. Each subtle indication functions as the person or company linking to your site approve of your blog or business. Backlinks tell Google that others approve of your content. Keyword: Backlinks.

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Labelling 40

The Social Pharmacist

JULY 28, 2022

The right tools help your overall social media management process push out great content and develop connections in real-time. Then, tag content for specific campaigns or label certain media types to maintain structure and keep your team on track. Approval workflows. Labeling systems. Shared calendars. Agorapulse.

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Labelling Customer Service Documentation 52

The Social Pharmacist

JULY 28, 2022

The right tools help your overall social media management process push out great content and develop connections in real-time. Then, tag content for specific campaigns or label certain media types to maintain structure and keep your team on track. Approval workflows. Labeling systems. Shared calendars. Agorapulse.

Labelling 52

Labelling Customer Service Community Pharmacies Documentation 52

The Social Pharmacist

JULY 28, 2022

The right tools help your overall social media management process push out great content and develop connections in real-time. Then, tag content for specific campaigns or label certain media types to maintain structure and keep your team on track. Approval workflows. Labeling systems. Shared calendars. Agorapulse.

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Labelling Customer Service Documentation 52

Pharmaceutical Technology

NOVEMBER 30, 2022

The drug was approved to treat type 2 diabetes mellitus in May. In the first quarter since its launch as an approved therapy for type 2 diabetes, Mounjaro has proven to be a lucrative drug, making $97.3 However, Novo Nordisk’s anti-obesity therapeutics have had rough rollouts following their approvals. million in Q3.

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Insurance Labelling Communication FDA 105

Pharmaceutical Technology

NOVEMBER 30, 2022

The drug was approved to treat type 2 diabetes mellitus in May. In the first quarter since its launch as an approved therapy for type 2 diabetes, Mounjaro has proven to be a lucrative drug, making $97.3 However, Novo Nordisk’s anti-obesity therapeutics have had rough rollouts following their approvals. million in Q3.

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Insurance Labelling Communication FDA 98

Pharmaceutical Technology

MARCH 17, 2023

Watt explained that for newer, first-in-class drugs these types of agreements can also give healthcare systems safety in their decisions to approve certain drugs. In some cases, she said, “[drug] innovation would have been otherwise hindered by their price tag alone”. Click here to watch this webinar and access the presentation.

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Pharmaceutical Companies Pharmaceutical Companies Communication 102