In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI™ for all indications matching the reference ...

insurance may not cover injection supplies, a person may not have insurance, or the pharmacy may only stock one syringe size (for example: 3 mL instead of 1 mL) and may make substitutions based on ...

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In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDItm for all indications matching the reference product Stelara® (ustekinumab) and has granted a provisional determination ...

US-based biopharmaceutical company Kashiv Biosciences has reported that a Phase I trial of its 125mg/mL pre-filled syringe injection, KSHB002, has achieved its primary endpoints. In the trial ...

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