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Alvotech signs U.S. agreement to expand access for newly approved high-concentration interchangeable biosimilar to Humira® (adalimumab)

Alvotech signs U.S. agreement to expand access for newly approved high-concentration interchangeable biosimilar to Humira® (adalimumab)
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Head-To-Head Comparison: Harpoon Therapeutics (NASDAQ:HARP) vs. LianBio (NASDAQ:LIAN)

Harpoon Therapeutics (NASDAQ:HARP – Get Free Report) and LianBio (NASDAQ:LIAN – Get Free Report) are both small-cap medical companies, but which is the better investment? We will compare the two businesses based on the strength of their risk, profitability, dividends, analyst recommendations, earnings, institutional ownership and valuation. Profitability This table compares Harpoon Therapeutics and LianBio’s […]

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Samsung Bioepis Presents Two Abstracts for Its Immunology Portfolio at the 2024 American Academy of Dermatology (AAD) Annual Meeting

Interchangeability study for HADLIMA (adalimumab-bwwd) was conducted in accordance with the FDA’s Guidance for Industry; primary pharmacokinetics (PK) endpoints as well as efficacy, safety and immunogenicity profiles were comparable between switching group and continuous reference product Humira group 52-week results from SB17 Phase 3 study demonstrated long-term efficacy, safety, and immunogenicity of SB17 compared to reference ustekinumab, including switching from ustekinumab to SB17 INCHEON,

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Samsung Bioepis Presents Two Abstracts for Its Immunology

Samsung Bioepis Presents Two Abstracts for Its Immunology
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U.S. FDA Accepts for Priority Review the Supplemental

Media Release COPENHAGEN, Denmark; February 27, 2024 FDA grants Priority Review with target action date of June 28, 2024Application based on results from...

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Genmab (GMAB) FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab

Genmab (GMAB) FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab
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U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY®) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma

U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY®) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
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U.S. FDA Accepts For Priority Review The Supplemental Biologics License Application For Epcoritamab (EPKINLY®) For Difficult-To-Treat Relapsed Or Refr...

U.S. FDA Accepts For Priority Review The Supplemental Biologics License Application For Epcoritamab (EPKINLY®) For Difficult-To-Treat Relapsed Or Refr...
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Genmab A/S: U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma

Genmab A/S: U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
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Alvotech and Teva Announce U.S. Approval of SIMLANDI® (adalimumab-ryvk) injection, the first interchangeable high-concentration, citrate-free biosimilar to Humira®

SIMLANDI is the first citrate-free, high-concentration biosimilar to be designated interchangeable to Humira in the U.S.

SIMLANDI is the first biosimilar approval under the strategic partnership...

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