Thu.Oct 31, 2024

article thumbnail

Access Insights 2024: The Value of Retail Consumerism

Pharmaceutical Commerce

Albert Thigpen, co-founder, Talentwise Consulting, shares how today’s consumer is empowered to make their own decisions as it relates to consumer choices in general, while outlining how the concept can be applicable to the healthcare and pharma industry.

59
article thumbnail

Evommune raises $115M to accelerate immune drug tests

Bio Pharma Dive

The biotech expects three Phase 2 readouts in urticaria and eczema over the next two years, and will keep its “options open” regarding an IPO, its CEO said.

Drugs 262
Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Reeves’ 2024 budget promises life sciences investment

Pharmaceutical Technology

Reeves' budget promised investment for innovation and R&D with a view to "harnessing the full potential of the UK’s science base”.

article thumbnail

Roche weighs whether speedy approval path is open for latest Alzheimer’s drug

Bio Pharma Dive

In an investor presentation, executives hinted at the possibility of seeking an accelerated approval of trontinemab if it can significantly lower levels of amyloid in a Phase 3 trial.

Drugs 184
article thumbnail

From Diagnosis to Delivery: How AI is Revolutionizing the Patient Experience

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

article thumbnail

Matinas BioPharma mulls wind-down as antifungal therapy deal falls through

Pharmaceutical Technology

The company has axed 80% of its staff and is considering a wind-down after the out-licencing deal of its lead antifungal was terminated.

130
130
article thumbnail

Jade, another biotech spinout of Paragon, to merge with Aerovate

Bio Pharma Dive

The immune disease drug developer expects to raise $300 million in a private financing set to close before its combination with the struggling Aerovate.

More Trending

article thumbnail

FDA’s new device chief faces challenges. Patient groups, industry are still optimistic.

Bio Pharma Dive

Patient advocates are hoping for change under new director Michelle Tarver, while industry groups hope she will build on former director Jeff Shuren’s leadership.

144
144
article thumbnail

Amgen earns higher revenues in Q3 2024, puts rare diseases in the spotlight

Pharmaceutical Technology

As the Horizon acquisition reaps its benefits, Amgen is now turning eyes to its obesity and diabetes portfolio.

130
130
article thumbnail

Compass delays anticipated psilocybin readout, cuts staff

Bio Pharma Dive

The company’s moves come after the FDA seemed to place a new hurdle in the path of psychedelic treatments for mental disorders.

144
144
article thumbnail

Community Pharmacies in Crisis: Navigating the Challenges and Closures

Pharmaceutical Commerce

With today's pharmacy landscape shaken by unprecedented and wider disruption to healthcare support and delivery, community and independent entities strive to remain an integral cog in the mix.

Pharmacy 123
article thumbnail

Optimizing Clinical Supply Strategy: Navigating Challenges & Finding Your Ideal Model

article thumbnail

As new drugs deliver, Bristol Myers CEO looks to 'further improve productivity and efficiency'

Fierce Pharma

Bristol Myers’ $1.5 billion restructuring initiative that runs through 2025 may not be the end of the company’s ongoing efficiency push. | Bristol Myers' $1.5 billion restructuring initiative that runs through 2025 may not be the end of the company's ongoing efficiency push. The drugmaker is "exploring opportunities to further improve productivity and efficiency," CEO Chris Boerner said Thursday.

article thumbnail

Why language training is crucial for healthcare teams

pharmaphorum

Effective language training for healthcare teams within the NHS is crucial for providing quality care and communication with diverse patient populations. Learn why it is essential for healthcare professionals.

104
104
article thumbnail

FDA removes Novo's Wegovy from shortage list, marking end of semaglutide supply rout in US

Fierce Pharma

Less than a month after the FDA removed Eli Lilly’s tirzepatide from its shortage list, the agency has done the same for Novo Nordisk’s rival GLP-1 semaglutide, potentially signaling the end of a d | The FDA this week revised its shortage list to note that the.25 mg starter dose of Novo’s semaglutide-based obesity med Wegovy is now available in the U.S.

Medicine 116
article thumbnail

Teva fined €462.6m for antitrust delay to MS drug rivals

pharmaphorum

The European Commission has delivered a hefty fine to Teva for abusing a dominant position in multiple sclerosis by artificially extending the patent protection for former blockbuster Copaxone.

Drugs 102
article thumbnail

The New Age of Decentralized Clinical Trials

White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations

article thumbnail

Gardasil's China troubles haunt Merck in Q3, with execs warning of more obstacles ahead

Fierce Pharma

While Merck's oncology powerhouse Keytruda delivered another multibillion-dollar sales haul in the third quarter, regional fright surrounding another staple product took the spotlight during the co | Despite the China growth woes, Merck is still confident it can achieve its $11 billion sales goal for the HPV vaccine by 2030.

Sales 115
article thumbnail

Alpha-9's $175m third-round heads latest biotech financings

pharmaphorum

Our latest round-up of financings in the biotech sector features Alpha-9 Oncology, Axonis, Kivu Bio, SynOx, Agomab, and Blue Earth Therapeutics.

109
109
article thumbnail

It's a monster MASH for Madrigal as Rezdiffra has caught on in a flash

Fierce Pharma

Forget about the “bumpiness” analysts expected from Madrigal Pharmaceuticals’ launch of potentia | Forget about the “bumpiness” analysts expected from Madrigal Pharmaceuticals’ launch of potential blockbuster Rezdiffra. In its second full quarter on the market, the fatty liver disease drug racked up sales of $62 million, which routed Wall Street's expectations and triggered a 16% surge in Madrigal's share price.

Sales 112
article thumbnail

Paragonix’s KidneyVault Gets FDA Clearance, Aims to Improve Kidney Preservation for Transplants

XTalks

Paragonix Technologies, an innovator in organ transport and preservation solutions, has received US Food and Drug Administration (FDA) 510(k) clearance for its KidneyVault Portable Renal Perfusion System. This clearance allows the KidneyVault system to be used in the US to improve the quality of kidney preservation and ultimately improve outcomes for patients undergoing kidney transplants.

article thumbnail

European Clinical Supply Planning: Balancing Cost, Flexibility and Time

article thumbnail

Regeneron's Eylea HD makes progress but doesn't dent the momentum of Roche's Vabysmo

Fierce Pharma

With U.S. | With U.S. sales of $392 million in the third quarter, Regeneron’s high-dose version of Eylea is closing in on blockbuster sales in its first full year on the market. The bad news for the company, however, is that while sales from Eylea HD increased by 29% sequentially, this didn't translate to a similar bump in overall U.S. revenue for the Eylea family of eye medications.

Sales 103
article thumbnail

Competitors race to launch GLP-1 drugs amid soaring weight loss demand

Outsourcing Pharma

Demand for weight loss drugs targeting GLP-1 has exploded in recent years, leading to disruptions in supply chains. Here are the companies racing for approval of their own versions of these highly coveted drugs.

Drugs 94
article thumbnail

Compass points to job cuts as it defers trial readouts

pharmaphorum

Compass Pathways will cut its headcount by 30% as it defers phase 3 readouts for its psychedelic therapy for treatment-resistant depression.

Trials 108
article thumbnail

Top 10 Medical Device Inventions of 2024, According to TIME

XTalks

Each year, TIME Magazine curates its “Best Inventions” list to showcase innovations that push the boundaries of technology, healthcare and everyday living. For the 2024 list , TIME collected nominations from editors, correspondents and industry experts using an open submission platform. Each nomination was evaluated on criteria including originality, effectiveness, ambition and impact.

article thumbnail

The New Age of Decentralized Clinical Trials

This new white paper defines and details the impact of Decentralized Clinical Trials on the Pharmaceutical industry and how the impact can be measured along with steps companies can take to ensure adoption.

article thumbnail

Nasdaq debutante Septerna swells its IPO to $331m

pharmaphorum

Septerna's protracted IPO on the Nasdaq has finally reached its conclusion, with the final amount raised by the GPCR-focused biotech above $331m

101
101
article thumbnail

Teva slapped with €463M fine over accusations it stymied Copaxone competition in Europe

Fierce Pharma

Some two years after the European Commission accused Teva of meddling with the competition for its former multiple sclerosis blockbuster Copaxone, the other shoe has finally dropped. | The European Commission has fined Teva 462.6 million euros over allegations that the company “[abused] its dominant market position to delay competition” to Copaxone across multiple EU member states.

article thumbnail

Lexeo shares dip on early data with Alzheimer's gene therapy

pharmaphorum

Lexeo reveals "promising" early data for gene therapy for APOE4-associated Alzheimer's, but shares in the biotech fall.

article thumbnail

NICE recommends remote monitoring technology for heart failure patients

Pharma Times

Heart failure accounted for approximately 90,000 hospital admissions in England in 2019 to 2020

108
108
article thumbnail

Unlocking Excellence: How Catalent Is Transforming Japan’s Clinical Research

Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud

article thumbnail

Axonis raises $115 million to overcome drug resistance in epilepsy

Outsourcing Pharma

The Boston-based startup Axonis Therapeutics has bagged $115 million in a Series A round to fuel its pipeline of treatments for pain, epilepsy and other conditions.

Drugs 82
article thumbnail

UK dementia clinical trial participation set to boost by ‘tens of thousands’

Pharma Times

The new Dementia Trials Accelerator is set to receive £20m of government funding

article thumbnail

How CDMOs are Transforming the Industry

Drug Patent Watch

The pharmaceutical industry has undergone significant transformations in recent years, driven by the COVID-19 pandemic and the subsequent need for rapid innovation and adaptation.

article thumbnail

AI Assistants, Agents and a New Era of AI in Life Sciences

Fierce Pharma

Author: Harietta Eleftherochorinou, Vice President, AI Strategy and Operations, IQVIA | We are entering a new era of AI in life sciences, where generative AI, conversational AI and AI agents are transforming day-to-day operations.

article thumbnail

How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.