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A partnership between University of Oxford, the Earlham Institute, and the global pharmaceuticalcompanies Biogen Inc and Boehringer Ingelheim is announced today to investigate a new drug target for the treatment of schizophrenia.
These digital twins allow pharmaceuticalcompanies to design clinical trials with fewer participants, while still providing reliable evidence to assess a drugs effectiveness. As a result, 2025 could be the year AI truly transforms the pharmaceutical sector.
The Swiss pharmaceuticalcompany has agreed to buy Televant, a company set up by Roivant and Pfizer to develop a promising inflammatory bowel disease treatment.
However, getting essential treatments to patients quickly and safely requires more than just technological innovation. A global network with local expertise To ensure the delivery of treatments to patients worldwide, biotech and biopharma companies also need partners that can provide comprehensive solutions from a geographic perspective.
Identifying branded drugs with a low likelihood of generic entry has become a crucial strategy for companies looking to expand their product portfolio through in-licensing. This approach not only helps maintain market exclusivity but also ensures a steady revenue stream for pharmaceuticalcompanies.
Finally, while there are clear front runners among the pharmaceuticalcompanies developing targeted therapeutics for these antigens there are also emerging biotechs aggressively pursuing these targets. Toxicities were challenging enough to cause 13% of patients to reduce dose or skip doses and 3% to discontinue treatment.
They might involve collaborations between pharmaceuticalcompanies, research institutions, and regulatory agencies. Whatever the form, the end result is the same: more effective, more affordable, and more accessible treatments for patients. Read more about the role of partnerships in generic drug development here: [link]
Obesity treatment is undergoing a major shift, much like the advances seen in cancer care. Phenomix Sciences , led by CEO Mark Bagnall, is using precision medicine to make treatments more targeted and effective. Phenomix Sciences, built on over a decade of clinical research at the Mayo Clinic, is disrupting this outdated approach.
One company that stands out is R-Pharm, a leading Russian pharmaceuticalcompany that has been at the forefront of innovation in the country. Another notable player is Pharmstandard, a Russian pharmaceuticalcompany that has been a pioneer in the development of innovative medicines.
This includes: Preclinical studies Clinical trials Regulatory approval Manufacturing and marketing Throughout this process, pharmaceuticalcompanies seek to protect their investments through patents.
Autoimmune diseases : Rheumatoid Arthritis : ADCs targeting specific immune cells or inflammatory mediators can provide more precise treatment options with potentially fewer side effects. Obesity : By targeting adipose tissue or specific metabolic pathways, ADCs could offer new treatments for obesity and related metabolic disorders.
Novartis Finalizes Acquisition of Regulus Therapeutics, Strengthening Its Renal Disease Portfolio with Promising ADPKD Therapy Novartis AG, a leading global pharmaceuticalcompany, has officially completed its acquisition of Regulus Therapeutics Inc. , a biotechnology firm known for its expertise in microRNA-targeting therapies.
A world where patients have access to life-saving medications sooner, and pharmaceuticalcompanies can bring new treatments to market faster. Will we see a surge in new treatments and medications? Imagine a world where generic drugs can be developed and approved in a fraction of the time it takes today.
Inspired by its success, pharmaceuticalcompanies are pursuing the development of drugs with similar therapeutic profiles, aiming to expand treatment options. Key Players and Challenges For pharmaceutical giants like Novo Nordisk and Eli Lilly, 2024 presents both opportunities and challenges.
Metastatic castration-resistant prostate cancer represents the most advanced and lethal form of the disease, defined by progression despite androgen deprivation therapy and subsequent ARPI treatment. This has created an urgent need for more effective and tolerable treatments for this population.
NASDAQ: SBFM), a pharmaceuticalcompany focused on developing and commercializing life-saving medicines across oncology, antiviral therapies, and other therapeutic areas, has announced the commercial launch of its first biosimilar drug, NIOPEG® , in Canada.
The weight loss industry has emerged as a major hub for innovative research, groundbreaking treatments, and economic opportunity. Mounjaro received approval as a treatment for diabetes in 2022, then in late 2023, under the brand name Zepbound (tirzepatide), it was approved for weight loss. With sales soaring to $2.2
We are proud that our partnership with Tsinghua University has set a benchmark for scientific research collaboration between multinational pharmaceuticalcompanies and high-profile academic institutions in China.
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18, 2020 /PRNewswire/ — Camurus AB (NASDAQ STO: CAMX) announced today that the Swiss agency for therapeutic products, Swissmedic, has approved weekly and monthly Buvidal ® prolonged release buprenorphine for the treatment of opioid dependence in adults and adolescents from 16 years of age. LUND, Sweden , Dec. About Buvidal.
It is becoming increasingly evident that generative artificial intelligence (GenAI) is a resourceful tool for helping pharmaceuticalcompanies reduce manual tasks required by clinical trials. This is especially relevant with today’s heavier focus on enhancing personalised medicine via broader emerging scientific findings.
Consider using a variety of claim types, including: Compound claims Method of treatment claims Formulation claims Dosage regimen claims Each type of claim offers different protections and can be valuable in different scenarios. Method claims related to diagnostic tests and personalized treatment regimens are becoming increasingly important.
By harnessing the vast amounts of data generated throughout the development pipeline, pharmaceuticalcompanies can accelerate the discovery of novel therapies, optimize clinical trial design, enhance drug safety monitoring, and deliver personalized medicine, ultimately improving patient outcomes and transforming the future of healthcare.
In emerging markets, where healthcare budgets are often stretched thin, generics have been a lifeline for patients who might otherwise go without the treatments they need. By investing in generic drug development, pharmaceuticalcompanies can tap into this lucrative market and make a real difference in the lives of millions.
Finally, while there are clear front runners among the pharmaceuticalcompanies developing targeted therapeutics for these antigens there are also emerging biotechs aggressively pursuing these targets. Each target and each therapeutic modality induces varying degrees of clinical efficacy, as well as causing toxicities.
Brain disorders are difficult to study and many drug candidates have failed in clinical trials, causing pharmaceuticalcompanies to reduce their investments or even exit the field entirely. But a new path for bringing treatments to patients is starting to emerge. We all recognize the vast, unmet medical need.
The search for effective treatments for neurodegenerative diseases like Parkinson’s disease has long been hindered by the brain’s complexity and the absence of adequate models for drug discovery. This approach has the potential to revolutionise clinical trial design and lead to more effective, personalised treatments.
Boehringer Ingelheim and Gubra today announced a new research and licensing agreement focused on the identification and validation of targets and innovative peptide compounds for the treatment of obesity. iii Current treatment options have limited efficacy in terms of weight loss or are often associated with adverse events. “We
Despite continuous innovations in the treatment landscape, unmet needs remain. Overall, the number of treatment-emergent adverse events reported was similar between the ponesimod and teriflunomide treated groups, and the majority were mild/moderate and did not warrant treatment discontinuation. vs. 9.4%), nasopharyngitis (19.3%
Astellas”) today announced topline results from the Phase 3 SKYLIGHT 4™ clinical trial investigating the long-term safety of fezolinetant, an investigational oral, nonhormonal compound being studied for the treatment of moderate to severe vasomotor symptoms associated with menopause (VMS) which will support future regulatory filing submissions.
Our lead program utilises OSK for the treatment of age-related optic neuropathies. a commercial stage pharmaceuticalcompany. a clinical-stage private biopharma company developing therapies for neurological and psychiatric diseases. What evidence is there that we can reverse aging with drugs?
The Strategic Role of CSOs in a Changing Pharmaceutical Landscape Pharmaceutical contract sales outsourcing is no longer viewed as a temporary or stop-gap measure. Equally important is regulatory compliance. Today’s CSOs are expected to adhere to frameworks like HIPAA , GDPR , the Sunshine Act , and regional promotional codes.
The Janssen PharmaceuticalCompanies of Johnson & Johnson today announced preliminary data from the Phase 1 CHRYSALIS study evaluating RYBREVANT TM (amivantamab-vmjw) for the treatment of patients with non-small cell lung cancer (NSCLC) with mesenchymal-epithelial transition (MET) exon 14 skipping (METex14) mutations.
Oral drug delivery remains the gold standard in pharmaceutical administration. It offers convenience for patients, promotes medication adherence, and improves treatment outcomes. This could aid in treatment for diabetic patients who currently rely on injections. This knowledge is instrumental in optimizing treatment plans.
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Takeda PharmaceuticalCompany Limited ( TSE:4502/NYSE:TAK ) (“Takeda”) today announced that it has submitted a New Drug Application (NDA) to the Ministry of Health, Labour and Welfare (MHLW) in Japan for lanadelumab subcutaneous injection, a monoclonal antibody therapy for prophylaxis against attacks of hereditary angioedema (HAE).
How do pharmaceuticalcompanies work with payers? In this blog post, we’ll take a closer look at how payer trends can reveal insights into the way patients use their medications – and how pharmaceuticalcompanies can use this data to help improve patient outcomes.
As the pharmaceutical and biotech industries continue to push for faster drug development, the importance of equity and diversity in clinical trial recruitment cannot be overlooked. With the rise of digital health and data, there are endless possibilities for reaching vulnerable populations and improving access to treatment.
While the primary goal of clinical trials is to help identify potential new treatments that improve people's health and save lives, it's the unfortunate truth that the patient experience is often not prioritized.
This deal means the French pharmaceuticalcompany will take full control of Principa, which includes its development of treatments for multiple sclerosis and a range of other autoimmune disorders. Sanofi is attempting to grow its pipeline of BTK inhibitors to rejuvenate the company by focusing on high priced medicines.
While this strategy is widely adopted by modern pharmaceuticalcompanies, in recent years, its effectiveness has begun to wane. This novel approach promises to create great advantages for the pharmaceuticalcompanies who adopt it and might become the future of medicine.
The FDA’s Response: A Real-World Study In response, the FDA sponsored a study that examined over 15,000 patients undergoing levothyroxine treatment[2]. The Plot: Generic vs. Brand-Name Two major pharmaceuticalcompanies sued over 10 generic drug manufacturers for infringing on a patent for their schizophrenia medication[4].
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Bioconjugates are rapidly emerging as a key frontier in targeted therapies, particularly through Antibody-Drug Conjugates (ADCs) , which combine antibodies with cytotoxic drugs to deliver more precise and effective treatments.
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