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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. On June 9, 2025, Secretary of Health and Human Services Robert F. June 9, 2025.
The new manufacturing lines will be operational in phases, with existing lines at the Suzhou and Rewari sites already functional since Q4 2024, and additional lines expected to start operations by Q3 2025. Thanks to their favorable dissolution rates, these capsules are valuable for developers of medicines and nutraceuticals.
Attorneys Office, Northern District of Illinois, April 21, 2025. Opioid prescriptions for high dosages and quantities, including prescriptions that individually or in combination, provide patients with daily dosages of greater than or equal to 300 Morphine Milligram Equivalents (MMEs). 81, 89, 251.
On June 15, 2025, Celltrion announced that the FDA has approved a new 45mg/0.5mL single-dose vial presentation of STEQEYMA (ustekinumab-stba) for subcutaneous injection. According to Celltrion, the new dosage form is intended to give physicians more flexibility while maintaining STEQEYMA’s safety and efficacy.
European geopolitical shifts In two installments of Pharmaceutical Technology ®’s “Industry Outlook 2025” series, Alexander Seyf, CEO and co-founder of Autolomous, and Edwin Stone, CEO of Cellular Origins, discussed European political impacts on the pharmaceutical industry at large, and the pharma supply chain in particular. June 12, 2025.
billion in 2025 to approximately $174.45 Packaging types generating demand in the market include tamper-proofing drug packaging against counterfeiting, as well as single-dosage packaging, according to the research. The worldwide pharmaceutical container packaging market is expected to rise in revenue from $104.12
On January 16, 2025, the FDA approved acalabrutinib (Calquence; AstraZeneca) in combination with bendamustine and rituximab for the treatment of adult patients with previously untreated mantle cell lymphoma (MCL) who are ineligible for autologous hematopoietic stem cell transplantation (HSCT). January 16, 2025. Accessed May 14, 2025.
In the same dosage group, further data showed that these participants lost an average of 16.0 Findings from the ATTAIN Phase III clinical trial programme investigating orforglipron as a tool for weight management will be shared later in 2025. Submission for the use of the drug to treat type 2 diabetes is expected next year.
Image credit: LASZLO | stock.adobe.com Gabrail et al presented data from a novel strategy involving continuous subcutaneous (SC) infusion of lenalidomide in a poster at the American Association for Cancer Research (AACR) Annual Meeting 2025 in Chicago, Illinois. Subscribe Now!
Morepen Laboratories has announced the launch of four new productsTicapen, UdoFix, LycoMore, and Acifix Raftin April 2025 for the Indian market. These launches form part of Morepens broader strategy to enhance its finished dosages segment while leveraging its internal research and development (R&D) capabilities.
Published June 27, 2025 Meagan Parrish Lead Editor post share post print email license Justin Sullivan via Getty Images Listen to the article 7 min This audio is auto-generated. 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.
Soefje, PharmD, MBA, BCOP, during the Hematology/Oncology Pharmacy Association (HOPA) 2025 Annual Conference in Portland, Oregon. Additionally, ANDA submissions should extrapolate the RLD safety and effectiveness data for drugs with the same active ingredients, dosage forms, strengths, routes, and labeling. REFERENCE Soefje SA.
Animal studies reveal dose-dependent hepatic responses to CBD, supporting the need for cautious monitoring even at consumer-relevant dosages. Pharmacists should review patient medication profiles, advise on appropriate dosage adjustments, and monitor for cumulative toxicity. of healthy adults, necessitating liver function monitoring.
SHOW MORE This abstract will be presented at the Oncology Pharmacists Connect (OPC) meeting in Austin, Texas, from June 19 to 20, 2025. CE hours from BCOP Updates 2024 and the Annual Conference 2025, featuring topics such as acute leukemia, cellular therapy for solid tumors, and the pharmacist’s role in serious illness conversations.
Patients with inflammatory conditions achieved similar clinical outcomes after switching from the reference adalimumab (Humira; AbbVie) to a biosimilar, according to real-world data presented at the 2025 American Society of Health-System Pharmacists Pharmacy Futures Meeting. Accessed June 26, 2025. June 12, 2025. June 7–11.
Generics are exact chemical copies of small-molecule drugs, with identical active ingredients, strengths, dosage forms, and routes of administration. Accessed May 13, 2025. Accessed May 13, 2025. Accessed May 13, 2025. Accessed May 13, 2025. REFERENCES 1. Updated June 20, 2024. Biosimilar medicines: overview.
The sNDA submitted July 8, 2025, is based on a phase 3 randomized withdrawal trial involving adults with stable schizophrenia who continued treatment with lumatperone for a 26-week double-blind phase. Time to relapse was significantly delayed in the lumatperone arm compared to placebo.
HME in drug manufacturing typically employs corotated twin extruders and uses heat and pressure to create solid dosage forms, dispersing the active pharmaceutical ingredient within a molten polymer matrix, and forming a solid solution or amorphous solid dispersion. Accessed May 27, 2025. May 21, 2025. Accessed May 27, 2025.
SHOW MORE This abstract will be presented at the Oncology Pharmacists Connect (OPC) meeting in Austin, Texas, from June 19 to 20, 2025. The abstract was originally shared at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago, Illinois. However, dosage modifications affect clinical outcomes.
Accessed May 15, 2025. Accessed May 15, 2025. Accessed May 15, 2025. Accessed May 15, 2025. Related Videos Related Content Advertisement June 20th 2025 OTC Case Studies: Summer Skin Care Sneha Baxi Srivastava, PharmD, BCACP, CDCES, DipACLM, FADCES Rupal Patel Mansukhani, PharmD, FAPhA, NCTTP June 3rd 2025 S2.
Challener News Article Pharmaceutical Technology Pharmaceutical Technology June 2025 Volume 49 Issue 5 Unique surface properties and ligand functionalization provide real advantages. 2025 19 (4). Efficient and effective delivery of complex and challenging drug substances is an ongoing issue facing developers of modern medicines.
2-4 In the United States, the FDA had approved 44 cell therapy products as of March 6, 2025. Accessed January 17, 2025. Accessed February 2025. March 6, 2025. Accessed May 12, 2025. Accessed January 15, 2025. Accessed January 15, 2025. Accessed January 15, 2025. Accessed January 20, 2025.
1 "[Meloxicam injection] demonstrates our commitment to improving patient care by providing an alternate dosage form for pain management," Ron Scarboro, chief executive officer at Azurity Pharmaceuticals, said in a press release. June 10, 2025. Accessed June 10, 2025. PR Newswire. Seminars in Arthritis and Rheumatism.
I recently had the opportunity to blend my own science and philosophy at the Hematology/Oncology Pharmacy Association (HOPA) 2025 Annual Conference in Portland, Oregon, presenting on psychedelic medicines in oncology and palliative care. Potential Roles of the Oncology Pharmacist My friend died of his metastatic cancer in early 2025.
Image Credit: Adobe Stock Images/Artur.com Key Takeaways Sanofi is shipping Beyfortus early to ensure strong supply for the 2025–2026 RSV season and avoid past shortages. As of now, supply for this coming season matches last year’s total dosage, with production expected to continue. June 9, 2025. Accessed June 9, 2025.
Limitations included open-label design and dosage constraints, but the multicountry approach enhanced generalizability and external validity. All patients underwent a 20-week correction period for dosage titration and Hb correction, which was followed by an 8-week evaluation for efficacy assessments. Accessed July 1, 2025.
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. Accessed June 13, 2025. June 12, 2025. Accessed June 13, 2025. Updated April 7, 2025. P = 0.04).
And in March 2025, Simtra head of Development Services Lidia Serina, PhD, spoke with Pharmaceutical Technology ® Group at the Drug, Chemical & Associated Technologies Association (DCAT) Week 2025 about the key challenges in aseptic processing for sterile injectables. June 11, 2025. June 10, 2025. Press Release.
By observing the microscopic effects of potential treatments, students will be able to gain insight into toxicity, dosage response, and disease progression. 2025, May 10). Retrieved May 12, 2025, from [link] -access/integrative-physiology- connection between-anatomy- and-function-107352.html. 2024, December). link] 022.02.002.
Selection of an appropriate OTC analgesic should take into consideration various patient factors, including the patient’s overall health status, current medical conditions, and medication profile, as well as patient preferences, which are often influenced by dosage form, required dosing intervals, and cost of OTC medication. December 2018.
On May 8, 2025, the Court of Appeals for the Third Circuit affirmed the district courts dismissal of AstraZenecas challenges to the Inflation Reduction Acts Drug Price Negotiation Program and CMSs Guidance implementing the Program.
June 27, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook Label updates have been approved for BMS’ CAR T cell therapies, Breyanzi and Abecma, to treat multiple myeloma. It is approved for the treatment of adult patients with relapsed or refractory multiple myeloma who have undergone two or more earlier lines of therapy.
In this article, well unpack the most effective SEO marketing strategies that align with pharma brands and the 2025 shifting strategyhelping you drive organic traffic while remaining compliant and trusted. H3: Use Persona-Based SEO Research In 2025, audience segmentation is evolving with AI-driven persona modeling.
Encelto (Neurotech Pharmaceuticals), which leverages an encapsulated cell therapy technology to continually deliver therapeutic doses of ciliary neurotrophic factor to the retina to treat macular telangiectasia type 2, received FDA approval in early 2025 (9). ClevelandClinic.org (accessed June 20, 2025). Press Release, March 6, 2025.
The data from an ongoing phase 1 LIMBER trial (NCT04279847) were presented at the 2025 American Society of Clinical Oncology Annual Meeting in Chicago. Updated June 12, 2025. Accessed June 30, 2025. 2025 ASCO Annual Meeting. May 30, 2025, to June 3, 2025. REFERENCES 1. Wang ZQ, Zhang ZC, Wu YY, et al.
Steqeyma provides a new dosage form and strength, enhancing treatment flexibility for young patients with chronic inflammatory conditions. June 15, 2025. Accessed June 16, 2025. Accessed June 16, 2025. Accessed June 16, 2025. March 12, 2025. Accessed June 16, 2025. Accessed June 16, 2025.
The investigators assessed a total of 90 patients who received talquetamab at a dosage of 0.8 mg/kg once every 2 weeks plus teclistamab at a dosage of 3.0 Updated May 23, 2025. Accessed June 16, 2025. June 15, 2025. Accessed June 16, 2025. European Hematology Association 2025 Congress. PR Newswire.
Results will be shared at the 2025 Oncology Pharmacists Connect meeting, potentially aiding oncology pharmacists in refining treatment strategies for sAML. SHOW MORE This abstract will be presented at the Oncology Pharmacists Connect (OPC) meeting in Austin, Texas, from June 19 to 20, 2025. HOPA has selected 4.0
April 14, 2025, LinkedIn Post. June 12, 2025. Recent Videos Related Content BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing. Spain’s Hospital-Based CAR-T Goes Global: A Therapy, a System, or a New Paradigm?
On April 18, 2025, Regeneron Pharmaceuticals announced that the U.S. The FDA disagreed with Regenerons proposal to add additional extended dosage intervals of greater than every 16 weeks, which is the maximum dosing interval on the currently approved label. Regeneron has not yet responded to the letter.
Compounding, by definition, involves customizing medications to meet individual patient needs, such as altering dosage forms or removing allergens. This all leads to an increased risk of adverse events, like contamination, incorrect dosages, or unexpected side effects, simply because production can vary wildly. May 30, 2025.
It co-developed Comirnaty, the COVID-19 vaccine in partnership with Pfizer, and is gearing up for the commercial launch of its variant-adapted COVID-19 vaccine for the 2025/2026 season, pending regulatory approval. In the US, seven patents are being assessed, and the trial is expected to start in September 2025. falciparum malaria.
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