BRISTOL MYERS SQUIBB

🇫🇷France
Ownership
-
Established
1989-01-01
Employees
30K
Market Cap
$97.5B
Website
https://www.bms.com/
nature.com
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Datopotamab–deruxtecan plus durvalumab in early-stage breast cancer

R.A.S., M.S.T., C.Y., R.N., H.S.R., M.D., A.J.C., E.S.-R., J.C.B., C.O., K.K., A.D.E., C.V., N.W., K.S.A., A.S.C., C.F., C.I., A.T., J.T., K.Y., L.H., K.G., F.M.H., T.S., A.L.A., P.B., P.N., G.L.H., W.F.S., J.P., P.P., A.D.M., D.Y., L.J.v.V., N.M.H., L.J.E. report various institutional research funding, advisory roles, consultancy, honoraria, patents, and stock ownership.
stocktitan.net
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Immunocore Holdings plc American Depositary Shares - IMCR

Immunocore Holdings plc (NASDAQ: IMCR) develops TCR bispecific immunotherapies for cancer, infectious, and autoimmune diseases using its ImmTAC platform. Notable products include KIMMTRAK for metastatic uveal melanoma. Recent collaborations include a Phase 3 trial with Bristol Myers Squibb for advanced cutaneous melanoma. The company's pipeline includes programs for HBV and solid tumors, with a mission to improve patient outcomes.
statnews.com
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BMS immunotherapy hits in lung cancer, advancing to Phase 3

Bristol Myers Squibb's Phase 2 RELATIVITY-104 trial showed improved responses in certain lung cancer patients when adding a second immunotherapy to existing checkpoint inhibitor and chemotherapy, leading to a Phase 3 study.
aacrjournals.org
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CSF1R Inhibition in Patients with Advanced Solid Tumors or Tenosynovial Giant Cell Tumor

Various researchers report financial relationships with pharmaceutical companies, including Deciphera, during and outside the conduct of the study.
biopharmadive.com
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Subcutaneous Tecentriq gets FDA OK; Gilead shot succeeds in second HIV trial

Roche's subcutaneous Tecentriq approved for cancer treatment; Gilead's twice-yearly HIV shot reduces infection risk by 96%; Biogen appoints Lloyd Minor and Menelas Pangalos as independent directors; Sanofi secures rights to a rare cancer radiopharmaceutical; Eli Lilly to expand Irish manufacturing for Alzheimer's drug Kisunla.
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.
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