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Phillips-Medisize Arkansas plant expands medtech capacity

April 25, 2019 By Nancy Crotti

PhillipsMedisizeupdated

Phillips-Medisize said today that it now has FDA-compliant manufacturing space in the Little Rock, Ark. plant of its parent company, Molex. The 380,000-square-foot facility is now fully compliant with the Current Good Manufacturing Practice (CGMP) regulations (21 CFR part 820) enforced by the FDA. The plant can now be used for Phillips-Medisize’s medical manufacturing services, including […]

Filed Under: Business/Financial News, Contract Services, Drug-Device Combinations, Food & Drug Administration (FDA), Regulatory/Compliance, Uncategorized Tagged With: FDA, Phillips-Medisize

Cigna lowers insulin price to $25 per month

April 3, 2019 By Nancy Crotti

Under pressure from patients and the FDA, Cigna (NYSE:CI) and Express Scripts said today that they will lower the price of insulin to $25 per month for some patients. Three firms — Eli Lilly, Novo Nordisk and Sanofi — control 90% of the global insulin market and produce all the insulin used in the U.S. […]

Filed Under: Business/Financial News, Diabetes, Featured, Food & Drug Administration (FDA), Uncategorized Tagged With: cigna, elililly, expressscripts, FDA, novonordisk, sanofi

PolarityTE launches two chronic wound treatment trials

April 2, 2019 By Nancy Crotti

PolarityTE (NSDQ:PTE) said it has begun enrolling patients in two new randomized clinical trials of its SkinTE regenerative tissue product for chronic wounds. The trials will evaluate the SkinTE’s effectiveness in treating diabetic foot ulcers (DFUs) and venous leg ulcers (VLUs).  SkinTE is a human cellular and tissue-based product designed to regenerate full-thickness, functional skin […]

Filed Under: Clinical Trials, Featured, Regenerative Medicine, Uncategorized, Wound Care Tagged With: polarityte

West Pharma’s SmartDose will deliver scPharmaceuticals’ edema drug

February 12, 2019 By Nancy Crotti

scPharmaceuticals

scPharmaceuticals’ (NSDQ:SCPH) has signed a development agreement to incorporate West Pharmaceutical Services’ (NYSE:WST) SmartDose drug delivery system with Furoscix, a drug that scPharmaceuticals developed to treat edema in heart failure patients. Burlington, Mass.-based scPharmaceuticals recently completed preliminary feasibility studies of the drug-device combination. The testing included drug stability in the pre-filled cartridge, drug compatibility, and […]

Filed Under: Business/Financial News, Cardiovascular, Drug-Device Combinations, Uncategorized Tagged With: scPharmaceuticals, West Pharmaceutical Services

Mylan wins race for generic Advair approval

January 31, 2019 By Nancy Crotti

Mylan logo - updated

FDA has approved the first generic of GlaxoSmithKline‘s (NYSE:GSK) blockbuster Advair respiratory drug, this one by Mylan (NSDQ:MYL), six months after rejecting Mylan’s application. Canonsburg, PA-based Mylan’s shares jumped 7% to $30.82 at market close after yesterday’s late-afternoon announcement, and were trading at $30.96 mid-morning today. GSK’s stock dipped 2% to$38.70 on the news late yesterday, but had […]

Filed Under: Business/Financial News, Drug-Device Combinations, Featured, Food & Drug Administration (FDA), Respiratory, Uncategorized, Wall Street Beat Tagged With: FDA, GlaxoSmithKline plc, Mylan, Novartis

FDA approves J&J’s Tremfya self-injection pen for psoriasis

January 30, 2019 By Nancy Crotti

FDA has approved Johnson & Johnson’s patient-controlled injector for Tremfya, a treatment for adults with moderate to severe plaque psoriasis. The self-injection approval may help Tremfya compete with AbbVie’s  (NYSE:ABBV) Humira pen, which was previously approved for self-injection by psoriasis patients. Made by J&J subsidiary Janssen Pharmaceuticals (Horsham, Penn.), Tremfya is a biologic therapy that selectively […]

Filed Under: Auto-injectors, Drug-Device Combinations, Food & Drug Administration (FDA), Uncategorized Tagged With: AbbVie, FDA, Janssen Pharmaceuticals, johnsonandjohnson

Rgenix raises $40M to develop novel cancer drugs

October 10, 2018 By Nancy Crotti

Biopharma startup Rgenix said it has raised $40 million in Series C financing to further develop its clinical and pre-clinical oncology programs and for general corporate purposes. New York City-based Rgenix has discovered several novel RNA-regulated cancer targets that drive tumor growth and cancer progression, according to its website. These targets regulate key components of […]

Filed Under: Funding Roundup, Oncology, Preclinical Trials, Uncategorized Tagged With: rgenix

Philips’ HealthSuite will track Ypsomed’s connected self-medication devices

October 5, 2018 By Nancy Crotti

  Philips and Ypsomed said today that they will jointly develop a solution for Ypsomed’s new self-medication adherence monitoring services based on Philips’ HealthSuite digital platform. The combination of Ypsomed’s connected devices and Philips’ (NYSE:PHG) cloud-based digital platform will allow Ypsomed’s pharmaceutical customers to deliver value-added services aimed at improving patient outcomes, the companies said in […]

Filed Under: Auto-injectors, Business/Financial News, Diabetes, Drug-Device Combinations, Research & Development, Technology, Uncategorized Tagged With: Philips, Ypsomed

One Drop wirelessly connects to Apple Watch

September 12, 2018 By Nancy Crotti

One Drop

One Drop said today that its wireless blood glucose monitoring system can now connect directly to Apple Watch, making it the first diabetes company’s system to do so. One Drop was also the first such company to launch a companion Apple Watch app, but until now, users had to manually log blood glucose, food, medication, […]

Filed Under: Big Data, Business/Financial News, Diabetes, Technology, Uncategorized Tagged With: Apple, onedrop

MicroPort’s drug-eluting stent performs well in European study

September 4, 2018 By Nancy Crotti

MicroPort Scientific’s Firehawk rapamycin target eluting coronary stent performed comparably to Abbott’s Xience stent family in a study just published in The Lancet. The TARGET AC multi-center, randomized controlled trial enrolled 1,653 patients at 21 clinical study sites in Europe. Firehawk met the trial’s non-inferiority primary endpoint of target lesion failure rate at 12 months of 6.1% versus […]

Filed Under: Cardiovascular, Clinical Trials, Drug-Device Combinations, Implants, Stents, Uncategorized Tagged With: abbott, microportscientific

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