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Moderna has been awarded $176 million by the Biomedical Advanced Research and Development Authority to accelerate development of messenger RNA-based pandemic influenza vaccines, the company announced in a statement Tuesday. Read the rest…
s CDC Vaccine Committee Overhaul for the Pharmaceutical Industry June 10, 2025 By Christopher Cole News Article The dismissal of all 17 members of the Advisory Committee on Immunization Practices has far-reaching impacts for the industry and beyond. Kennedy Jr.
Hyderabad-based Indian Immunologicals (IIL) announced the launch of its pediatric dose of indigenous Hepatitis A vaccine, Havisure (0.5 IIL organised free Hepatitis A vaccination drives for children in two orphanages in Hyderabad to start with, which includes one specifically for blind children.
ImmunityBio has licensed technology underpinning a COVID-19 vaccine that could be administered orally rather than by injection from UK biotech iosBio. Non-injectables remove the need for health professional-led immunisation programmes, making widespread vaccine roll-outs quicker and easier and more affordable,” Channon told pharmaphorum.
Sanofi and GlaxoSmithKline are restarting clinical development of their COVID-19 vaccine, which was delayed after hitting a snag late last year. In December interim phase 1/2 trial results showed the vaccine produced a lower immune response in older adults.
The Brazilian Health Regulatory Agency (Anvisa) has granted emergency use authorization for Sinovac Biotech’s Covid-19 vaccine, CoronaVac, in children aged three to five years. Subjects in this age group can receive the same vaccinedosage authorised in patients aged six to 17 years, as well as adults.
Two trials ( Phase I and Phase II ) of a vaccine given to healthy adults from Mali has demonstrated its potential as a safe and effective way to immunise against malaria, prior to and during pregnancy. In one trial, the PfSPZ vaccine was evaluated in 300 healthy women ages 18 to 38 years.
AstraZeneca is to run an additional global trial to test its COVID-19 vaccine at a lower dosage, as the UK regulator begins to review trial data. Health secretary Matt Hancock has asked the UK’s regulator the Medicines and Healthcare products Regulatory Agency (MHRA) to begin its review of the vaccine.
Health Canada has granted authorisation for Pfizer ’s unit Pfizer Canada and BioNTech’s Covid-19 vaccine, Comirnaty, as a three 3?g This dosage was chosen as the preferred dose in children aged under five years based on safety, tolerability and immunogenicity findings. g paediatric vaccine doses following the authorisation.
Pfizer and BioNTech have filed an application seeking Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) for a booster dosage of an Omicron BA.4/BA.5-adapted 5-adapted bivalent vaccine for Covid-19 in people aged 12 years and above. 1-adapted vaccine. 5-adapted bivalent vaccine.
When it comes to vaccines and other high-value biologics, it is essential that effective formulations go hand in hand with safe delivery. This also has clear advantages in healthcare settings, particularly when it comes to vaccines. In general, a prefilled syringe is clearly preferred for vaccines.”. A new challenge .
A group of experts will present an encore abstract titled " Prevalence of Dosage Modifications and Impact on Response Milestone Among Patients With CML Treated With Imatinib Using Real-World Data " at the 2025 Oncology Pharmacists Connect (OPC) meeting in Austin, Texas, from June 19 to 20.
There are two different-sized doses for Beyfortus, depending on a baby’s weight, and a single dosage of Enflonsia used for all babies. While the price points are the same, the two products have differences. That could give the product an advantage in that pediatricians would not have to worry about giving the wrong dose to a baby.
Other PrEP regimens on the market require daily oral dosages or shots every few months, but the latest version is only administered twice a year. A long-time leader in vaccines, the U.K. The FDA approved the updated formulation, which will be sold under the brand name Yeztugo, earlier this month.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines Feliza Mirasol April 30th 2024 Podcast In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
.” Dr Veeramani, Chairman, Pharmexcil, said “ The Indian pharmaceutical industry stands as a global leader, exporting to over 200 countries and providing comprehensive solutions across APIs, finished dosages, clinical research, and pharmacovigilance. With exports nearing $27.84
How to get it right -A practical framework Start with a Risk Assessment: Map out materials, dosage form, route of administration, and expected interactions. Real example: Injectable in a glass vial We supported a vaccine company using Type I glass vials they assumed were inert. Many Indian companies skip this step.
All these challenges tend to lead to high costs for therapeutics and vaccines leveraging nanoscale drug delivery systems. The improved targeting capability of nanoscale delivery systems also leads to improved activation of immune cells in cancer vaccines.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines Feliza Mirasol April 30th 2024 Podcast In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
A magnifying glass examining a vintage vaccine vial surrounded by four minimalistic chart icons, symbolizing healthcare, medicine, and analytics in the context of global health monitoring.
While some speculate the move is related to an ongoing patent dispute, the panel suggested the transaction also reflects broader strategic concerns, including a cooling vaccine market and a desire to bolster oncology capabilities and mRNA manufacturing scale.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines Feliza Mirasol April 30th 2024 Podcast In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines Feliza Mirasol April 30th 2024 Podcast In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines Feliza Mirasol April 30th 2024 Podcast In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
The second most commonly used pharmaceutical dosage form, capsules, are anticipated to be a $5.2 Compared with other oral solid dosage forms (OSDs), capsules also offer the easiest method to achieve fixed-dose combinations (FDCs) of incompatible drug substances. Dr Bhat : As with any dosage form there are benefits and drawbacks.
Pharmacists offer personalized advice on common womens needs, whether understanding the dosage or side effects of medication or helping them make informed choices regarding their unique health circumstances. As womens health needs change over time, the need for screening conditions becomes more important.
Dosage: Adults, elders, and children 16 years and over: Two tablets up to four times a day with a maximum of 8 tablets/ day. Apply 4 hours as a minimum safe interval between dosages. Dosage: Menstruating women above 12 years: One-Two tablets up to three times a day as needed with a maximum of 6 tablets in 24 hours.
H3: Use Keywords With Compliance in Mind Branded terms like Dupixent for eczema or Entresto heart failure dosage can rank well, but they require regulatory scrutiny. Brands supporting vaccination awareness or community clinics benefit from optimizing location-specific content.
However, during the second half, the surge in demand for vaccines to fight the coronavirus enhanced the industry’s need for raw materials and product intermediates of API molecules. However, due to the small volumes required for dosage, small-scale providers are also gaining importance, findings from the report show.
In addition, the dosage [of 2000 IU per day] used in the research is far below the target dose for correcting vitamin D deficiency, which is usually 50,000 IU per week,” Carvalho-Pessoa said in a news release. 1,2 “Even with a small sample of participants, it was possible to observe a significant difference in the response to chemotherapy.
Last month, European Commission approved the new subcutaneous (SC) formulation of Bristol Myers Squibb’s (BMS) Opdivo (nivolumab) with a dosage strength of 600 mg/vial, expanding treatment options for various adult solid tumours. Sign up for our daily news round-up! Give your business an edge with our leading industry insights.
Vaccination No Vaccine for the common cold Vaccines are available to help prevent the flu. Follow the recommended dosage and avoid exceeding the daily limit. Pay attention to the dosage, frequency, and any warnings or interactions. Stay hydrated: Drink plenty of fluids to stay hydrated and help thin mucus.
Research has reported that fear of needles constitutes about 20-50 per cent among children and 20-30 per cent among adults globally; often leading to missed vaccinations and delayed treatments. How does the company collaborate with pharma and vaccine companies to optimise efficacy of medicines with this delivery system?
The extraordinary scenario of producing vaccines for a global pandemic led to a well-documented shortage of vials, stoppers, and syringes, and finding a solution is no easy task. And while there are occasional discussions about pharma companies re-shoring API production facilities, the process would be extremely expensive and complex.
According to the authors, self-amplifying RNA (saRNA) could be a next-generation vaccine platform, but it requires smart drug delivery vehicles to maintain the long-term stability and efficiency of the drug. The current NA dosage forms and novel DDSs have enabled the successful launch of NA therapeutics globally. Ingle et al.
The spectrum of such products includes new chemical entities (NCE), new drugs with new indications or new routes of administration or new dosage forms, modified or sustained release formulations, novel drug delivery forms, vaccines, medical devices, and in-vitro diagnostic medical devices.
Additionally, ANDA submissions should extrapolate the RLD safety and effectiveness data for drugs with the same active ingredients, dosage forms, strengths, routes, and labeling. In the 505(j) ANDA approval pathway, on the other hand, submissions can be multisource generic drugs; however, this pathway requires bioequivalence to the RLD.
CCI is the ability of a container closure system to maintain the sterility of final pharma, biological and vaccine products throughout their shelf life. Otherwise, the presence of oxygen can lead to the breakdown of fats, lipids, proteins, and other ingredients, compromising the drug formulation and impact of the dosage.
Steqeyma provides a new dosage form and strength, enhancing treatment flexibility for young patients with chronic inflammatory conditions. The biosimilar demonstrated comparable efficacy and safety to Stelara in a phase 3 clinical trial, supporting its FDA approval.
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