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Immunocore Holdings Limited: Immunocore presents phase 3 data comparing tebentafusp with investigator's choice in the clinical trial plenary session at the American Association for Cancer Research 2021 Annual Meeting

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PRESS RELEASE
Immunocore presents phase 3 data comparing tebentafusp with investigator s choice in the clinical trial plenary session at the
American Association for Cancer Research 2021 Annual Meeting
Tebentafusp is the first investigational therapy to improve Overall Survival (OS) in patients with metastatic uveal melanoma
First positive Phase 3 clinical trial for any T cell receptor therapeutic and first for any bispecific in a solid tumor
(Nasdaq: IMCR), a late-stage biotechnology company pioneering the development of a novel class of T cell receptor (TCR) bispecific immunotherapies designed to treat a broad range of diseases, including cancer, infectious and autoimmune disease, presented data from a phase 3 randomized trial comparing tebentafusp (IMCgp100) with investigator s choice in first-line metastatic uveal melanoma (mUM) in the clinical trial plenary session at the American Association for Cancer Research (AACR) Annual Meeting 2021. ....

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[특징주]SK바이오사이언스 등 K백신 주목 '급등'

[특징주]SK바이오사이언스 등 K백신 주목 '급등'
edaily.co.kr - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from edaily.co.kr Daily Mail and Mail on Sunday newspapers.

United States , Lee Ji Hyun , Life Sciences , United States Clinical , ஒன்றுபட்டது மாநிலங்களில் , லீ ஜி யுங் , வாழ்க்கை அறிவியல் , ஒன்றுபட்டது மாநிலங்களில் மருத்துவ ,

Dante Labs achieves ISO 13485 certification for its Genomic Interpretation Software Immensa, leveraging an 18 month long clinical validation study of 500,000 samples

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Dante Labs, a world leader in genomic sequencing and data analysis, announced today that it received ISO 13485:2016 certification for its Immensa Genomic Interpretation Software as a medical device. The highly coveted industry certification involved a deep clinical validation study carried out by several teams at Dante Labs over an 18 month period. The accreditation was awarded by The British Standards Institution (BSI) Group.
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210405005027/en/
Dante Labs Automatic Lab (Photo: Business Wire)
This is a great achievement for all of the team members at Dante Labs who worked very hard to implement a brand-new ISO-compliant quality system and develop the software, says Dante Labs CEO Andrea Riposati. The bioinformatics team ran a clinical validation study the size of a population genomics program. ....

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Novavax Initiates COVID - 19 Vaccine Clinical Trial Crossover

Novavax Initiates COVID - 19 Vaccine Clinical Trial Crossover
(Di martedì 6 aprile 2021) . today announced the initiation of
Crossover arms in two ongoing
Clinical
Trials of NVX - CoV2373, . NVX - CoV2373 contains purified protein antigen and can neither replicate, nor can it cause
COVID - . ....

Novavax Initiates , Clinical Trial Crossover , Co Vid , மருத்துவ சோதனை குறுக்குவழி , இணை வித் ,

Moleculin Biotech Engages IQVIA To Manage Potential COVID-19 Clinical Trial

Moleculin Biotech Engages IQVIA To Manage Potential COVID-19 Clinical Trial
SOUTH SAN FRANCISCO (dpa-AFX) - Moleculin Biotech Inc. (MBRX) said that it has engaged IQVIA Biotech, a contract research organization, to manage the company s effort to begin potential clinical trials of WP1122 for the treatment of COVID-19.
WP1122 is a prodrug of 2-DG, a well-known antimetabolite with the ability to inhibit glycolysis and alter glycosylation, two processes critical to coronaviruses like SARS-CoV-2, the virus responsible for COVID-19.
The company noted that 2-DG has shown activity against SARS-CoV-2, other coronaviruses and other non-coronaviruses. But the company believes its therapeutic potential is limited by its inherent lack of drug-like properties. ....

Moleculin Biotech Inc , Co Vid , இணை வித் ,