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As the pharmaceutical industry continues to evolve, drugdevelopers encounter new challenges and opportunities in their pursuit of innovation. These annual results provide valuable insights into the state of drugdevelopment, highlighting shifts in industry practices and illuminating emergent areas of focus.
Our annual look at the state of the drugdevelopment industry highlights a dual set of challenges complicating progress. Rising costs have become a persistent challenge for drugdevelopers, driven by a combination of internal and external pressures that have intensified in recent years.
As the clinical trial landscape evolves, drugdevelopers are faced with novel challenges and changes in study recruitment, trial size and structure, and more. The adoption of new innovations, strategies and technologies offers opportunities to address persistent challenges and develop suitable approaches for the future.
The PPD clinical research business of Thermo Fisher Scientific has surveyed more than 150 drugdevelopers around the globe to gather annual data on trends in pharmaceutical research and development. Applying artificial intelligence (AI) to drugdevelopment (e.g.,
The world of drug discovery is in a state of transformation, with advancements in biotechnology opening doors to new possibilities for targeting previously "undruggable" disease mechanisms. Addressing Industry Challenges We then dig into the broader challenges the pharmaceutical industry is facing in drug discovery and development.
The PPD clinical research business of Thermo Fisher Scientific conducts an annual survey of more than 150 leaders at pharmaceutical companies around the globe to assess trends in drug discovery and development, including preferences around outsourcing and functional service provider (FSP) utilization.
During drugdevelopment, active pharmaceutical ingredients are often formulated as salts to provide the final pharmaceutical product. From the database with SQL In the downloaded database, the drug mechanism may be mapped to a single member of the compound family in the drug_mechanism table, typically the approved form.
15, 2020 /PRNewswire/ — Armata Pharmaceuticals , Inc. Patrick , Chief Executive Officer of Armata Pharmaceuticals.
About Armata Pharmaceuticals, Inc.
Armata is committed to advancing phage with drugdevelopment expertise that spans bench to clinic including in-house phage specific GMP manufacturing. .
28, 2021 /PRNewswire/ — CASI Pharmaceuticals (Formerly Known As EntreMed, Inc.).
About CASI Pharmaceuticals.
CASI Pharmaceuticals, Inc. The Company’s operations in China are conducted through its wholly-owned subsidiary, CASI Pharmaceuticals ( China ) Co., and BEIJING , Jan.
Fast Track designation facilitates the development and expedites the review of drugs that are intended to treat serious and life-threatening conditions and show the potential to fill an unmet medical need. A preprint supporting Brilacidin’s COVID-19 treatment potential can be downloaded at the link below.
Source link.
27, 2021 /PRNewswire/ — Armata Pharmaceuticals , Inc.
About Armata Pharmaceuticals, Inc.
In addition, in collaboration with Merck, known as MSD outside of the United States and Canada , Armata is developing proprietary synthetic phage candidates to target an undisclosed infectious disease agent.
With a team of more than 300 AI professionals, including data scientists, data engineers, AI architects, and AI developers, Perficient has extensive knowledge and skills in various AI domains. Download the Forrester report, The AI Services Landscape, Q1 2024 to learn more (available to Forrester subscribers and for purchase).
To view the full announcement, including downloadable images, bios, and more, click here. Key Takeaways:
CEO Laurie Heilmann will be presenting the strategic roadmap for accelerating growth of tech-enabled drug discovery in cancer.
Click image above to view full announcement.
When conducting first-in-human (FIH) clinical trials, small to midsize pharmaceutical and biotechnology companies are faced with several crucial choices that can shape the trajectory of their drugdevelopment pathway. For additional insights, download our full white paper, “ First-in-Human Studies: IND or CTA? ”.
As the clinical research landscape continually evolves, the choice of a Contract Research Organization (CRO) partner can significantly impact the success of drugdevelopment programs. Discover how Worldwide is positioned to meet your needs with agility, expertise, and a truly personalized approach.
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Psychedelic Pharmaceutical Scientist and Clinical Pharmacologist Robert Barrow Appointed as Chief Development Officer.
Mr. Barrow has over a decade of experience leading drugdevelopment programs aimed at identifying and testing novel treatments in a wide range of disease conditions under FDA and EMA.
” “Dynacure is a leader in rare disease drugdevelopment, as evidenced by its lead product candidate DYN101, which is in clinical development for the treatment of Myotubular and Centronuclear Myopathies for which there are no FDA or EMA approved therapeutics,” said Ms. Previously, Ms. Prior to Merrimack, Ms.
Roquinimex (Linomide), a drugdeveloped by Pfizer for the treatment of multiple sclerosis, is structurally related to laquinimod. Figure 3: Roquinimex (linomide) Clinical development of both laquinimod and roquinimex was halted due to serious cardiovascular events. Teva Pharmaceuticals licensed laquinimod from Active Biotech.
Our new directors are well-recognized for their leadership and accomplishments in the biopharmaceutical, biotechnology and pharmaceutical industries, as well as in public capital markets and corporate governance.” Russell served as a director of Endocyte, a Nasdaq-listed public company acquired by Novartis, and AMAG Pharmaceuticals.
Nasdaq: MBRX) (Moleculin or the Company), a clinical stage pharmaceutical company with a broad portfolio of drug candidates targeting highly resistant tumors and viruses, today announced that the US Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to Annamycin for treatment of soft tissue sarcomas. .
She most recently comes from a position as Senior Medical Director at Ferring Pharmaceuticals in Copenhagen. Dr Reimer will replace Dr Charlotte Russel and be overall medically responsible for Alligator’s drugdevelopment candidates, with an emphasis on bringing mitazalimab and ATOR-1017 into Phase II efficacy studies.
who brings to the Company over 25 years of neuroscience leadership experience in the pharmaceutical and biotech industries, including most recently as Chief Operating Officer of Therachon Holding AG until its acquisition by Pfizer in July 2019. View original content to download multimedia: [link]. SOURCE Corlieve Therapeutics.
Dr. Liu shared his over 30 years of R&D experience in drugdevelopment both in the global pharmaceutical companies and world renowned scientific research institutions. By joining Innovent, Dr. Liu will be responsible for global R & D, pipeline strategy, business development and international operations.
As drug molecules become more complex so do the options to deliver them. This novel nanoparticle formation technology provides hope for improving the possibilities and probabilities of developing better medicines for patients and it expands Nanoform’s reach into the growing biological market. HELSINKI , Nov. ” Prof.
8, 2020 /PRNewswire/ — At its Investor Day yesterday, Ionis Pharmaceuticals, Inc. ” Dr. Monia continued, “For years we have been recognized for our excellence in research, early drugdevelopment and scientific innovation. About Ionis Pharmaceuticals, Inc. SOURCE Ionis Pharmaceuticals, Inc.
At the beginning of 2023, the PPD clinical research business of Thermo Fisher Scientific surveyed 120 drugdevelopers across the pharmaceutical, biopharmaceutical and biotechnology sectors (referred to collectively as “pharma”) to learn more about sponsors’ current needs for site and patient recruitment services.
Perficient is listed as a medium-sized consultancy with our industry focus being industrial products, pharmaceuticals and medical equipment, and retail. To find out more, download the Forrester Commerce Services Landscape, and contact our commerce experts today.
Drugdevelopers need to staff RA teams that can handle regular lifecycle maintenance ebbs and flows across lifecycle maintenance tasks, and plan for a workload that sometimes requires senior-level expertise, while at other times is much more suited to support staff. However, completing this work is only half the challenge.
18 , 2021 /PRNewswire/ — Hanmi Pharmaceutical Co., plans to create a global R&D achievement based on innovations of inflammation–fibrosis treatment, Triple-acting new drug for NASH (non-alcoholic steatohepatitis) treatment as well as various other innovations in metabolic disease, oncology and rare disease fields.
Drug Channels readers will save $200 off the standard rate when they use code ZZX688 and register prior to November 13th.*. You can download the complete agenda here. Visit www.raredisease-summit.com for further details and to register. David Fajgenbaum, M.D., Visit www.raredisease-summit.com for further details and to register.
patent is part of a patent family, exclusively licensed from Ionis Pharmaceuticals, which covers modulators of DNM2 expression. The Dynacure team leverages its proven track record in rare disease drugdevelopment to build a pipeline of novel drug candidates. View original content to download multimedia: [link].
The pharmaceutical industry stands at an exciting crossroads, with groundbreaking innovations in drug discovery and delivery redefining what’s possible in patient care. Innovating Beyond Challenges: Emerging Therapies and Technologies The evolution of drug delivery systems tells a compelling story of human ingenuity.
The weakened dose of phages helped bacteria develop resistance, and the trial became yet another study that provided evidence phages are safe, but little more. Phages that can be essentially downloaded and synthesized by anyone, in any location, would solve those problems, he says. 4 But the same barriers still exist today. .
Pharmaceutical, biotechnology and medical device companies have been uniquely impacted by the Covid-19 pandemic, posing both opportunities and challenges for the life sciences industry. Source link.
TOMI-T1D is an international partnership between academia, the pharmaceutical industry and nonprofit organizations. The project also seeks to engage the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) to identify opportunities for regulatory endorsement of such drugdevelopment tools.
Unlocking the Potential of Biocatalysis The pharmaceutical industry is evolving, and biocatalysis is at the forefront of this transformation. Access our comprehensive guide to learn how drug manufacturers can create more sustainable, cost-effective, and efficient production processes by harnessing natures catalystsenzymes and cells.
Planning the journey from data to deliverables The future of AI-enabled drugdevelopment benefits from the continued advancement of multimodality and clinical genomics, with a focus on integration, efficiency and personalisation to transform both care and R&D.
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