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Results from the head-to-head study showed treatment with Zepbound resulted in 47% greater relative weight loss than Wegovy, a finding that could advantage Lilly in the companies’ market competition.
We just finished talking to over 200 hundred HCPs about pharma marketing and salespeople to measure any differences since before the pandemic. Attitudes are indeed changing, but one need remains clear: access to data obtained during clinical and ongoing trials. Will they transform their HCP marketing or stick to dated models?
The post Small Pharma stock market launch funds DMT-based depression drugtrial appeared first on. “Given most other psychedelics focused companies have only been formed in the last 2 years, we believe our focus on IP since inception in 2015 gives us the potential to build a robust portfolio of valuable assets,” he added.
86% of diagnostic device companies, 65% of pharma marketers, and over half of biotechs use social as a critical part of their marketing mix to reach HCPs. The best approach is to use social media to connect HCPs to clincial information and drugtrials. Doximity was flagged for having anti-vaccine information.
Under the terms of its ongoing collaboration agreement with GSK, Immutep is eligible to receive up to a total of £54 million in remaining developmental milestone payments, as well as single-digit tiered royalties, if GSK2831781 is marketed.
Unlike commercial pharmaceutical packaging, the primary consideration in clinical trial packaging is protecting the product quality and reliability for research. Finding the best clinical trial packaging services providers.
Amid a period of clinical holds and legal tangles, the US antibody specialist CytoDyn has reached a settlement to resolve legal disputes with its former contract research organization (CRO) Amarex Clinical Research.
A former employee of Tellus Clinical Research in Miami has admitted to charges related to a conspiracy to falsify data on a list of clinical drugtrials.
A Florida doctor has been sent to prison after submitting a false affidavit claiming she had screened children in a clinical study looking at the effectiveness of drugs given to children with asthma when she had not.
Shares of Zealand Pharma experienced a significant surge, jumping 16% as the market opened on Monday, following the release of groundbreaking phase II trial results for an experimental obesity treatment being developed in collaboration with Boehringer Ingelheim.
With the acquisition MindMed gains access to HealthMode’s intellectual property, platforms for clinical drugtrials, and its entire 24-strong digital medicine team. MindMed will buy HealthMode in a cash and shares deal that values the digital firm at around CAD $41.3 ($32.2
Use your energy where it’s needed most — ensuring that your products are in compliance and getting to market as quickly as possible. Don’t waste your time on unending, unproductive online searches for news stories, reports and opinion; let DID’s experienced in-house editorial team do the work for you.
And a fragmented clinical trials industry has made it a prime target for private equity, which often consolidates markets by merging companies. To date, 11 of the 25 private equity firms identified by industry tracker PitchBook as the top investors in health care have bought stakes in clinical research companies.
Several factors make it difficult for HTA bodies often to assess orphan drugs, including a lack of robust trial data due to difficulties in finding patients, the absence of randomised controlled trials, the use of surrogate endpoints, and the lack of active drug comparators. Source: CRA Analysis.
It was our third time receiving the award, which recognizes the fastest-growing mid-market businesses in the state. For a clinical trials organization to achieve this level of scale is notable. Many people don’t even realize they may qualify for a trial or how it could benefit them.
LinkedIn has evolved into a critical tool for pharma marketing professionals to build meaningful relationships. Start by ensuring your headline and summary clearly state your role in pharma marketing. Incorporate SEO-friendly keywords like pharma marketing , drug commercialization , and healthcare innovations.
Pharmacovigilance refers to the practice of collecting, detecting, assessing, monitoring and preventing adverse effects (AEs) caused by new drug substances.
The need for new medical treatments and drugs has never been greater. But before pharmaceutical companies can go to market with a breakthrough drug, they need to ensure safety and efficacy through clinical trials. Even reaching the clinical trial phase offers no guarantees, as only 12% of such drugs receive U.S.
According to the FDA’s 2020 DrugTrials Snapshot Report , only 8% of clinical trial participants are Black or African American, as compared to nearly 14% of the US population. The fact is, many minorities never learn about vital clinical trials in play, or that they’re eligible to participate. About the author.
COVID-19 spurred a significant increase in Virtual Pre-Site inquiries to accommodate site monitoring for existing studies and to expedite study startups for COVID and other drugtrials. Working together we can bring better medications to market more quickly. To learn more about VirTrial, visit [link].
Upon starting the phase 2 trial in March, Visus targeted the delivery of top-line data in mid-2021. The slight slip could see Visus fall further behind Eyenovia and, in particular, AbbVie in the race to get a presbyopia treatment to market.
The greater the risk, the more likely a series of trials for market clearance or approval will be required. These products will require clinical trial data to get to market, but with significantly fewer participants required as compared to a drugtrial.
In 2024, there have been significant pharma and biotech layoffs as companies restructure to navigate financial challenges and shifting market dynamics. Takeda has forecasted continued financial pressure but is banking on new drugtrials to stabilize its position. What’s Driving the Pharma and Biotech Layoffs?
This morning I ran across a bit of a coffee-spitter : in the middle of an otherwise opaquely underinformative press release fromTranscelerate Biopharma about the launch of their Counterfeits flooding the market? citation needed ] And on that point, I think we can agree: Citation needed. I hope the folks at Transcelerate will oblige.
(CDS), a leading technology provider focused on data collection and clinical trial management, today announced several updates in celebration of its tenth anniversary, including the company’s latest technological development, TrialKit AI, a machine-learning API. About Crucial Data Solutions.
The drug development process is a lengthy and time-intensive process that ends up causing fortunes to industries and organizations sponsoring the process. According to a study by the Tufts Centre for the Study of Drug Development, approximately USD 2.6B Regulatory agencies have always prioritized the well-being of the patients.
“Biopharmaceutical industry insiders frequently have access to material non-public information about mergers, drugtrials, or regulatory approvals that impacts the stock price of not only their company, but also other companies in the industry,” said Gurbir Grewal, director of the SEC’s Enforcement Division.
CDC and new drugs have fostered an era of mistrust with some people. DTC marketers need to be more forthcoming when it comes to drugtrials and side effects. So how should DTC marketers view this? We need to talk more about clinical trials to understand terms and reassure a public that is skeptical of new drugs.
Some Phase I trials are also first-in-human (FIH) studies, meaning the treatment has not previously been tested in people. Approval confirms the experimental drug or therapy meets the government’s standards for safety and efficacy, and can be used to treat patients outside of clinical trials.
LNPs are an adaptable, modular technology and when combined with microfluidic mixing, have the potential to accelerate development and commercialisation timelines and provide drug developers with an early foothold into a largely untapped market. This is what SUT offers.” Please check your email to download the Whitepaper.
Regeneron resumes enrollment in lymphoma drugtrials ( Reuters ).
Incyte’s vitiligo treatment meets main goal in late-stage trial ( Reuters ).
$DNA is once again on NYSE; FDA clears Soliris challenger for the market; Flagship’s thinking big again with eRNA; and more ( Endpoints ).
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