MedPath

BRISTOL MYERS SQUIBB

🇫🇷France
Ownership
-
Established
1989-01-01
Employees
30K
Market Cap
$97.5B
Website
https://www.bms.com/
morningstar.com
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Halozyme Announces FDA Approval of Roche's Subcutaneous OCREVUS ZUNOVO™ with ...

FDA approves Roche's OCREVUS ZUNOVO™ with Halozyme's ENHANZE® for RMS and PPMS, offering a 10-minute subcutaneous injection.
prweb.com
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Trialbee Adds Industry Authority John Murray-Pryce to Its Distinguished Advisory Board

John joins Trialbee for its global team, industry-leading patient recruitment platform, and Swedish culture, aiming to contribute to equity in clinical research.
prnewswire.com
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Halozyme Announces FDA Approval of Roche's Subcutaneous OCREVUS ZUNOVO™

Roche received FDA approval for OCREVUS ZUNOVO™, a subcutaneous injection using Halozyme's ENHANZE® technology for RMS and PPMS, offering a 10-minute, twice-a-year treatment.
globenewswire.com
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7MM Migraine Drug Market Forecast and Analysis to 2033

The 'Migraine: Seven-Market Drug Forecast and Market Analysis' report, added to ResearchAndMarkets.com's offering, forecasts the migraine market in the US, France, Germany, Italy, Spain, the UK, and Japan to grow from $9.2 billion in 2023 to $16.4 billion by 2033, driven by a 6.0% CAGR. The report covers epidemiology, treatment options, unmet needs, pipeline analysis, and market competition.
quantisnow.com
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Halozyme Announces FDA Approval of Roche's Tecentriq Hybreza™ With ENHANZE®

Halozyme announces FDA approval for Roche's Tecentriq Hybreza™, a subcutaneous anti-PD-(L)1 immunotherapy using ENHANZE® technology, offering faster administration and broader treatment options for lung, liver, skin, and soft tissue cancers.
stocktitan.net
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Halozyme Announces FDA Approval of Roche's Tecentriq Hybreza™ With ENHANZE® for ...

FDA approves Roche's Tecentriq Hybreza™, a subcutaneous anti-PD-(L)1 immunotherapy using Halozyme's ENHANZE® technology, reducing injection time to 7 minutes from 30-60 minutes for IV infusion, available for adult indications of IV Tecentriq® in the U.S.
benzinga.com
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Gearing up for the European Society for Medical Oncology (ESMO24) Congress with OBiS

OBiS Insights pre-meeting ESMO24 report profiles 275 new, unapproved cancer drugs, classified as 40% antibody-based, 37% small molecule, and 23% mixed bag. The report excludes drugs not in abstract titles and will update during the conference. 43% of these drugs were discussed at recent ASCO24 meetings.
eurekalert.org
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BMI's relation to cancer therapy mortality risks not so straightforward

Immunotherapy less risky for non-small cell lung cancer patients with BMI under 28, while chemotherapy is optimal for those with BMI 28 or higher, according to Osaka Metropolitan University study.
geneonline.com
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Illumina's IVD Biomarker Test Becomes the First FDA-approved Pan-cancer Companion

Illumina's TruSight Oncology Comprehensive, an FDA-approved IVD biomarker test kit, detects variants in 517 genes across nearly 30 solid tumor types, enabling personalized targeted therapies and faster treatment interventions within 4-5 days.
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