Thu.Feb 01, 2024

article thumbnail

Roche shuffles early stage pipeline as it joins obesity rush

Bio Pharma Dive

Roche said it was shelving those drugs in favor of experimental programs to treat obesity that it gained from its takeover of Carmot Therapeutics.

Drugs 292
article thumbnail

Keytruda remains Merck & Co’s biggest 2023 success story as patent expiry looms

Pharmaceutical Technology

Merck & Co (MSD) has reported a 1% revenue increase from 2022, and may face setbacks in the next few years from top-selling drugs.

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

Sanofi appoints Nestlé executive as new finance chief

Bio Pharma Dive

François-Xavier Roger will replace current CFO Jean-Baptiste Chasseloup de Chatillon as Sanofi continues a research pivot and cost-cutting drive.

Research 265
article thumbnail

Novartis reports 62% rise in FY 2023 net income

Pharmaceutical Technology

Novartis has announced net income soaring by 62% to $8.6bn for the full year 2023 (FY 2023) from the previous year’s $6.04bn.

246
246
article thumbnail

European Clinical Supply Planning: Balancing Cost, Flexibility and Time

article thumbnail

Takeda pays $300M to license Protagonist drug for blood disorder

Bio Pharma Dive

The agreement gives Protagonist an experienced hand in Takeda, which can help the former commercialize its product.

Licensing 273
article thumbnail

Vivet wins $5.3m grant to develop gene therapy for rare metabolic disorder

Pharmaceutical Technology

The French government grant will cover preclinical and clinical research for Vivet’s gene therapy for cerebrotendinous xanthomatosis.

More Trending

article thumbnail

NeoPhore adds $12.2m in Series B extension for immuno-oncology pipeline

Pharmaceutical Technology

The financing extension brings Series B total funding to $39.5m, helping advance the UK company’s lead DNA MMR protein candidate.

DNA 147
article thumbnail

Who's No. 1? With $25B in sales, Merck's Keytruda looks to be the top-selling drug of 2023

Fierce Pharma

With Merck reporting a whopping $25 billion sales haul for | With Merck reporting a whopping $25 billion sales haul for Keytruda on Thursday, the PD-1 cancer superstar appears to be the world’s top-selling drug in 2023. Keytruda looks set to take over the top spot from Pfizer and BioNTech’s Comirnaty, which ruled the previous two years, scoring sales of $55.9 billion in 2022 and $55.1 billion in 2021.

Sales 113
article thumbnail

Almirall and Microsoft partner for dermatological drug development

Pharmaceutical Technology

Almirall has entered a strategic collaboration with Microsoft to steer innovation and digital transformation in dermatology.

article thumbnail

In-person, hybrid, or digital? State of pharma meetings and events in 2024

pharmaphorum

Explore the current state of pharmaceutical meetings and events in 2024, including the shift from in-person to virtual and hybrid formats. Discover how the industry is embracing diversity, equity, and inclusion in these gatherings.

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

UK MHRA approves GSK’s momelotinib for myelofibrosis anaemia

Pharmaceutical Technology

The UK MHRA has approved the use of GSK’s momelotinib (Omjjara) for moderate to severe anaemia in adult patients with myelofibrosis.

130
130
article thumbnail

Lundbeck study knocks confidence in alpha-syn as CNS target

pharmaphorum

A phase 2 trial of Lundbeck’s alpha-synuclein-targeting drug Lu AF82422 has failed to reach statistical significance in patients with multiple system atrophy (MSA), although the company says there are encouraging “signals of efficacy” in the data.

Trials 108
article thumbnail

Takeda and Protagonist sign rusfertide development deal

Pharmaceutical Technology

Takeda has entered a global licence and partnership agreement with Protagonist Therapeutics for developing and marketing rusfertide.

article thumbnail

Making connections and getting noticed as a biotech start-up

pharmaphorum

On today's podcast, brought to you by Kadans Science Partners, host Jonah Comstock is joined by Bradley Hardiman, Astellas Pharma’s Senior Director of Business Development; Mike Murray, head of Murray International Partners Ltd; and Mairi Dillon, Kadans' Ecosystem Manager for UK & Ireland.

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

The new technologies helping biopharmaceutical trailblazers accelerate progress from research to market

Pharmaceutical Technology

Getting new drugs out of the research phase, and into clinical studies and commercialization, is an odyssey in quality control

Research 130
article thumbnail

Beyond chemotherapy: Navigating the promise and perils of CAR-T therapy in pediatric cancer

BioPharma Reporter

Upon hearing the phrase âcancer treatmentâ, the first word that can typically spring to mind is chemotherapy â a primary therapy which uses powerful chemicals to destroy rapidly growing cancer cells in the body.

article thumbnail

Healthcare providers favour pricing control as US drug costs soar

Pharmaceutical Technology

GlobalData reports that HCPs predict a continued increase in drug prices, as inflationary pressures rise.

Drugs 130
article thumbnail

Merck still in the market for deals in the $1B to $15B range, CEO says

Fierce Pharma

Even after the acquisitions of Prometheus and Acceleron, Merck is ready to make more deals in the $1 to $15 billion range, according to CEO Rob Davis.

Marketing 115
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

Excellence Awards Report 2023

Pharmaceutical Technology

Our Awards and Rankings report is available now to download

130
130
article thumbnail

£9.6M for NeoPhore's small molecule inhibitors targeting MMR pathway that could prevent cancer

Outsourcing Pharma

A company building a pipeline of small molecule drugs targeting novel proteins across the DNA mismatch repair (pathway) has announced a further extension to its series B financing round.

DNA 105
article thumbnail

Excellence Awards Report 2023

Pharmaceutical Technology

Our Awards and Rankings report is available now to download

130
130
article thumbnail

Startup founded to help an 'NHS in crisis' by creating digital clinics accessed as easily as online banking

Outsourcing Pharma

A husband-and-wife team keen to find a solution to an âNHS in crisisâ have secured $1.5 million in seed funding for their UK-based startup providing AI-powered clinical and drug prescription services for minor conditions.

Drugs 102
article thumbnail

Roles and Responsibilities of Specialized Clinical Supply Experts

When selecting a clinical supply provider, consideration often focuses upon the manufacturing, packaging, storage and distribution capabilities available that will, at face-value, be sufficient to meet the needs of the sponsor and their trial. However, there are human-based and knowledge-driven factors that are often overlooked that go beyond these basic physical capabilities and are integral to the development and delivery of high performing clinical supply chains.

article thumbnail

Healthcare sector cybersecurity retrospective and the year ahead

pharmaphorum

As cyberattacks continue to target the healthcare sector, it is crucial to look back at cybersecurity incidents from the past year and prepare for the challenges that lie ahead. This retrospective discusses the impact on patients, health systems, insurers, and vendors, and highlights the importance of cybersecurity measures in protecting sensitive healthcare information.

102
102
article thumbnail

In Medicare negotiation process, HHS sends 1st price offers as industry blasts lack of transparency

Fierce Pharma

Despite litigation and denouncements from the biopharma industry, Medicare price negotiations under the Inflation Reduction Act are rolling on. | Despite litigation and denouncements from the biopharma industry, Medicare price negotiations under the Inflation Reduction Act are rolling on. And today, the government is sending out its first round of offers on affected drugs.

Drugs 101
article thumbnail

Positive pre-IND meeting with FDA for new ovarian cancer cell therapy

BioPharma Reporter

Cartherics, a biotechnology company developing immune cell therapies for the treatment of cancer, has completed a pre-investigational new drug (pre-IND) meeting with the FDA for a phase 1/2 clinical trial of its cell therapy product, CTH-401 for the treatment of ovarian cancer.

article thumbnail

Sanofi expects RSV antibody to ?breach blockbuster status in 2024, even as supply hitch drags on

Fierce Pharma

As Sanofi strives to become a global immunology leader, it's also busy making the most of a crucial respiratory launch with partner AstraZeneca. | As Sanofi strives to become a global immunology leader, it's also busy making the most of a crucial respiratory launch with partner AstraZeneca. On both fronts, Sanofi expects to see dividends in 2024.

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.

article thumbnail

Cancer treatment could identify patients most likely to respond to cancer drugs

Pharma Times

Tumours with high mtDNA mutations more likely to respond to Opdivo

Drugs 141
article thumbnail

Despite Roche's sharp COVID sales decline, eye drug Vabysmo powers major revenue win, CEO says

Fierce Pharma

As Roche CEO Thomas Schinecker sees it, the Swiss pharma made a “major achievement” in 2023. Despite a sharp decline in COVID-related sales, the company was able to grow overall revenues | As Roche CEO Thomas Schinecker sees it, the Swiss pharma made a “major achievement” in 2023. Despite a sharp decline in COVID-related sales, the company was able to grow overall revenues thanks in large part to the performance of eye disease drug Vabysmo.

Sales 92
article thumbnail

Almirall, Microsoft team up on digital dermatology drive

pharmaphorum

Almirall has formed a three-year alliance with Microsoft designed to accelerate the discovery and development of personalised dermatology therapies.

article thumbnail

GSK inks another Zantac settlement ahead of trial in California

Fierce Pharma

After GSK spent the latter half of 2023 warding off concerns about the swelling Zantac product liability litigation, the company is back at the settlement table in 2024. | After GSK spent the latter half of 2023 warding off concerns about the swelling Zantac product liability litigation, the company is back at the settlement table in 2024.

Trials 88
article thumbnail

Accelerating Clinical Supply Through Integrated Drug Development

As the development pipeline for new drugs continues to grow, biopharmaceutical companies are re-evaluating how to best manage and balance resources across an increasing number of development projects and complex clinical trials. There are two approaches that can be used to speed a drug from development to clinic faster: timeline compression and parallel processing, but only one that considers the benefits of integrating clinical supply into the overall drug development process.