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Adalimumab Clinical Trial Updates

LexBlog IP

In July 2022, clinical trial data was published from a real-life retrospective observational study of pediatric (<18 years) and geriatric (≥65 years) patients with psoriasis in Italy. A total of 11 children and 23 elderly psoriasis patients were enrolled. Patients received either adalimumab or etanercept biosimilars.

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Time to look Beyond Compulsory Licenses? A Glimpse at the Ribociclib Case

SpicyIP

[ This post is authored by SpicyIP Intern Tejaswini Kaushal with inputs and comments from Swaraj and Praharsh. In July 2021, the wife was diagnosed with metastatic HR+/HER2- Breast Cancer, for which she was prescribed Ribociclib (INR 58,140 per month), Letrozole (INR 1027.75 Tejaswini is a 3rd-year B.A. of GDP in FY23.

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EMA Accepts MAA for Dong-A ST’s Ustekinumab Biosimilar

LexBlog IP

On July 14, Dong-A ST announced that the European Medicines Agency accepted its Marketing Authorization Application (MAA) for DMB-3115, a biosimilar referencing STELARA (ustekinumab). STELARA is approved for the treatment of plaque psoriasis, psoriatic arthritis, Crohn’s disease, and ulcerative colitis.

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Diagnosing the Future of Telemedicine: COVID-19-Motivated Regulation Changes Should be Permanently Adopted

LexBlog IP

As the world came to a screeching halt, healthcare providers and essential businesses were tasked with maintaining function while protecting patients, employees, and customers amidst a rapidly changing health and technological landscape. Telemedicine is the use of telecommunications to deliver medical care to patients from a distance.

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Fish Attorneys Author Biosimilar Development Article, “Regulatory And Legislative Actions Set The Tone For Biosimilars In 2021”

Fish & Richardson Trademark & Copyright Thoughts

Fish attorneys Jenny Shmuel , Philip Chen , and Kayleigh McGlynn authored a Biosimilar Development article, “ Regulatory And Legislative Actions Set The Tone For Biosimilars In 2021.” Already, FDA has licensed almost 30 biosimilars, nearly 20 of which are available to patients in the United States. Biosimilar Regulatory Updates.

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An Outline on South Africa and India’s WTO IP waiver

IP and Legal Filings

However, the proposal observes that Intellectual Property Rights (IPR) has managed to potentially hinder the timely provisioning of affordable medical products and facilities to COVID 19 patients. TRIPS Council meeting, which was held on 20 th July 2021. LinkedIn.

IP 52
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No "German injunction gap" expedition in Abbott v Dexcom global diabetes battle, as Mr Justice Mellor expresses "some regret"

The IPKat

Most UK diabetes patients monitor their glucose levels using the "fingerprick" method. But around 30% of patients require the more sophisticated method called "continuous glucose monitoring" or CGM. Abbott commenced its expedition application on 14 July to expedite its revocation claim of four of Dexcom's patents.