Pharmaceutical Technology

MAY 19, 2023

The US Food and Drug Administration (FDA) has approved AbbVie’s Rinvoq (upadacitinib) for patients with Crohn’s disease who do not respond to TNF blockers, a common immune suppressant treatment for the condition. Data from two Phase III studies, U-EXCEED and U-EXCEL, involving 857 patients was used to support the approval.

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Food and Drug Administration FDA Sales Food 105

pharmaphorum

JANUARY 10, 2023

Astellas has licensed rights to a drug developed by Selecta Biosciences that could make more patients eligible for treatment with its gene therapy for inherited neuromuscular disorder Pompe disease. There has been no update from Astellas since the clinical hold was imposed last June.

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Patients FDA 119

European Pharmaceutical Review

FEBRUARY 8, 2023

The number of blood cancer patients receiving CD19-directed CAR-T therapies is set to boom over the next decade from approximately 3,700 patients in 2021 to nearly 13,500 patients in 2031. This allows for a large total eligible patient population despite capturing less patient share relative to other CD19 CAR-T agents.

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Marketing Sales Physicians Patients 98

European Pharmaceutical Review

JULY 18, 2022

Nebido is also patented until March 2024 in the European Union and until May 2027 in the United States. Too few of these patients receive appropriate treatment. We are committed to facilitating access to treatment for even more patients in need,” commented Gabriel Baertschi, CEO of Grünenthal.

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Medicine Physicians Competition Patients 98

European Pharmaceutical Review

MAY 4, 2023

Data announced at the European Lung Cancer Congress (ELCC) earlier this month revealed the long-term efficacy and safety of RYBREVANT ® (amivantamab) in patients with post-platinum EGFR Ex20ins-mutated advanced non-small cell lung cancer (NSCLC). 3 , 4 There is a high unmet need for novel and targeted therapies for this patient population.

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Food and Drug Administration Safety Patients Medicine 98

European Pharmaceutical Review

DECEMBER 2, 2022

The facility is planned for completion in 2027. We continue to invest in our global manufacturing infrastructure to bring much-needed medicines and vaccines to patients, around the world, and to deliver the next scientific breakthroughs.”. In 2021, the company invested €40 million in its Grange Castle facility. The post Pfizer’s €1.2

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European Pharmaceutical Review

JUNE 15, 2023

Importantly, they identify potential sources of microbial contamination and assess their risk to patients. This microbial contamination can lead to a range of adverse events, such as infections, adverse reactions, or device failures, which can compromise patient safety and health outcomes. Sharma et al.

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Manufacturing Medical Safety Transportation 103

European Pharmaceutical Review

NOVEMBER 20, 2023

This will ensure that patients have rapid access to new treatment options and make us more independent from fragile supply chains,” commented Professor Dr Karl Lauterbach, Federal Minister of Health. But we will continue to improve the framework conditions for research and production.

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European Pharmaceutical Review

JANUARY 19, 2023

The contribution will enable the programme to reach additional physicians and medical students, further expanding the initiative that aims to extend the reach of clinical trials in underserved patient populations in US communities. The Winn Award Program has so far trained 114 early-stage investigator physicians.

Food and Drug Administration 98

Food and Drug Administration Physicians Medicine Food 98

European Pharmaceutical Review

JANUARY 10, 2023

Treatments identified in the report are predicted to be potential blockbuster drugs by 2027 or have potential to serve unmet patient needs for millions of patients worldwide. The drug can be used to treat a niche group of patients with high unmet need.

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Food and Drug Administration FDA Food Medicine 98

European Pharmaceutical Review

NOVEMBER 18, 2024

Furthermore, to address the demand due to more transplant patients worldwide, the company highlighted developed a new manufacturing process to increase production capacity, enhancing the reliability of supply and lowering Thymoglubulin’s environmental impact. These will be available for marketing from 2027, according to Sanofi.

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European Pharmaceutical Review

DECEMBER 16, 2024

Construction is expected to be finished in 2027, the pharma company confirmed. The investment will also provide economic benefit, with 400 permanent jobs anticipated to be generated following completion of the site.

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Manufacturing Pharmaceutical Pharma Patients 52

PM360

JULY 13, 2023

1 This increased technology spending has led to industry fragmentation, creating siloed data—which can leave providers with an incomplete picture of a patient’s health record—and an often-cumbersome experience for patients, leaving them to shoulder the burden of managing their own care. billion in 2020 and is expected to reach $381.7

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European Pharmaceutical Review

SEPTEMBER 28, 2023

EMA prepares for winter antibiotic shortages PFAS restriction in pharmaceutical manufacturing In its current form, the procedure currently underway could lead to a ban on all PFASs by 2027, with very limited derogations, EFPIA acknowledged. The organisation’s response included results from a patient impact analysis.

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Pharmaceutical manufacturing Manufacturing Pharmaceutical Medicine 105

Impetus Digital

MARCH 15, 2024

In 2022, global spending on cancer medicines was approximately 196 billion USD, and this number is forecasted to reach $375 billion by 2027. In fact, for the past five years, the number of treated patients with cancer has seen an average annual increase of 5% globally (1). The field of oncology is rapidly growing and evolving.

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Recruitment Healthcare Provider Patients Healthcare 78

Medico Reach

DECEMBER 2, 2022

billion , and by 2027, it is expected to reach around an exciting amount of 115.1 from 2022 to 2027. Some clinical trials offered by PPD include: Early Development Consulting and Product Development PPD Biotech PPD FSP The site and patient-centered Solutions Clinical Development. billion with a CAGR of 11.0% Medpace Holdings.

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Medico Reach

APRIL 5, 2022

The use of IoT has grown exponentially in the field of Medicine providing better services to patients. This has transformed the way we analyze Medical Data , Patient information, and Medical device information. between 2022-2027. This along with remote supervision will create a 50% reduction in patient readmissions.

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PM360

SEPTEMBER 21, 2023

This article covers some of the reasons these drugs were chosen, how the process for price negotiation will occur, and the impact for the industry and for patients. Over the next few weeks, manufacturers will submit a range of clinical, marketing, sales, pricing, and patient data, and then meet with CMS to discuss submissions later this fall.

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PM360

MAY 21, 2024

From connecting with patients by interactive ads to dabbling into cross-platform integration, here is what our specialists had to say. What are new and effective ways of engaging patients who are now using streaming services? What are new and effective ways of engaging patients who are now using streaming services?

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Media Healthcare Healthcare Marketing 105

Penrod

APRIL 1, 2024

These policies aim to enhance prior authorization and efficiency for care providers, payers and patients. CMS has extended payers’ compliance dates to the new rule to January 2027, giving payers more time for implementation. Payers would be required to expand patient access APIs and implement Provider Access APIs.

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Electronics Insurance Healthcare Healthcare 52

pharmaphorum

JANUARY 16, 2023

Even where there has been innovation, for example in cholesterol lowering with PCSK-9s and the siRNA treatment Leqvio, the vast majority of patients are on generic versions of medicines launched in the 1990s, and innovative medicines have not transformed the treatment paradigm. Innovation will power the market.

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PM360

JUNE 29, 2022

But to succeed, players must deeply understand both the end-to-end consumer and patient experience and create an ecosystem of partners to deliver the care, products, and experiences that health-conscious consumers need. Prescription refills can now be placed with a simple click on a patient portal. Reconsider the Role of Packaging.

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Retail Marketing Healthcare Healthcare 97

European Pharmaceutical Review

MARCH 4, 2024

percent through 2027. Therefore, biologics identification and characterisation poses unparalleled challenges, as does their manufacturing processes and routes of administration while maintaining patient safety and clinical efficacy. Standardising isolation, purification and storage processes are crucial areas for further improvement.

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Food and Drug Administration Transportation FDA Medical 98

pharmaphorum

SEPTEMBER 23, 2022

In a statement , Ionis said that AZD8233 met its objectives in the phase 2b SOLANO trial in patients with hypercholesterolaemia, when given as a monthly 60mg dose, reducing LDL-C levels by 62% compared to placebo after 28 weeks, and thereby achieving the study’s primary endpoint. billion in sales by 2027, ahead of Repatha at $2.2

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Sales Education Pharma Patients 59

European Pharmaceutical Review

APRIL 14, 2023

billion by 2027… In five years and beyond… The event closed with further enthusiasm. It does take a community to move a drug into patients.” “There are challenges to overcome, but the depth of excitement around the field is such that the financing will come. That will solve problems and oligonucleotides will move forward.”

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Manufacturing Consulting Pharmaceutical Marketing 98

European Pharmaceutical Review

FEBRUARY 22, 2023

1 Used to treat a range of chronic diseases (eg, diabetes, rheumatoid arthritis, psoriasis, Crohn’s disease, haemophilia, etc), it is projected that the sales of biologics will rise from $380 billion in 2022 to $416 billion in 2023, and to almost $600 billion in 2027. We have confirmed this in close to 100 subjects who have swallowed the RP.”

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Food and Drug Administration Manufacturing Safety Pharmaceutical 105

pharmaphorum

NOVEMBER 18, 2022

At its second attempt, Provention Bio has secured FDA approval for teplizumab, as a treatment to delay late-stage type 1 diabetes (T1D) in at-risk individuals – becoming the first disease-modifying therapy for these patients. Teplizumab is thought to work by preventing the activation of T cells that attack those cells.

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FDA Patients Manufacturing Sales 52

Medico Reach

SEPTEMBER 12, 2022

Upon immediately subjecting the patient to an X-ray, the barium appears white as doctors observe how it outlines the digestive tract. . Option to treat the patient during endoscopy. But since the patient is already sedated while performing the procedure, the doctor can treat the problem during endoscopy. billion by 2027.

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pharmaphorum

JULY 18, 2022

If approved, atogepant is expected to be a strong competitor to Vydura, according to analysts at GlobalData, who point to strong clinical data in episodic and chronic migraine and the availability of three strengths that allows the dose to be more closely matched to a patient’s needs.

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Sales Marketing Patients FDA 52

LEVO Health

JULY 15, 2024

billion by 2027. To stand out in this competitive landscape, businesses must focus on patient engagement, comprehensive service offerings, strong marketing and branding, and strategic partnerships with top-tier telehealth service providers like WellSync and medical marketing experts like Levo Health.

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Pharmaceutical Technology

DECEMBER 16, 2022

GnRH antagonists have an improved safety and efficacy profile compared to the marketed GnRH agonists, which have significant side effects that are unappealing to patients. This therapy is currently in Phase II development and is expected to launch in the US and 5EU in 2027 and 2028, respectively.

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Marketing Side effects Sales Safety 59

pharmaphorum

SEPTEMBER 22, 2022

The “US-first” mindset will lead to higher proportions of American patients in its clinical trials and investment in “capability and talent” in the US, where it aims to become a top-five player by 2027 – a big advance on its current 10th place. billion by 2024.

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Management Sales Patients Marketing 52

pharmaphorum

OCTOBER 1, 2022

The latest judgments relate to an attempt by Chinese drugmaker HEC Pharma to bring a generic version of fingolimod to market in the US, and Novartis defense of the 9,187, 405 patent which expires in December 2027.

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Competition Pharma Marketing Sales 52

pharmaphorum

JULY 18, 2022

. “The acceptance of the filing of proposed biosimilar natalizumab by the European regulatory authorities means we are a critical step closer to getting this important medicine to the patients who need it the most,” said Polpharma Biologics’ chief executive Michael Soldan in a statement.

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pharmaphorum

JANUARY 9, 2023

Albireo secured approval in the US and Europe for the ileal bile acid transport inhibitor (IBATi) drug in 2021 for the treatment of pruritus (itching) in patients with rare disorder progressive familial intrahepatic cholestasis (PFIC), and has said sales should reach $24 million this year.

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Transportation Sales Leads FDA 52

PM360

DECEMBER 14, 2022

In its latest venture into the healthcare arena, Amazon is reaching out directly to the consumer via its soon-to-be-launched Amazon Clinic , a virtual health service for patients to see licensed clinicians about common medical issues. billion euros into its new facility where it is planning to hire 400 and 500 new personal by 2027.

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Manufacturing Medical Healthcare Healthcare 52

European Pharmaceutical Review

OCTOBER 12, 2023

With the goal of supplying cell therapies, vaccines and other essential medicines such as antibody drugs to patients, the facilities aim to address major supply challenges and navigate the intricacies of producing fragile biological products. Meath opened last month.

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