FDA approves Basilea’s antibiotic Zevtera for three indications
The approval for Zevtera was based on the clinical efficacy and safety data from the Phase 3 ERADICATE…
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04 Apr 24
The approval for Zevtera was based on the clinical efficacy and safety data from the Phase 3 ERADICATE…
03 Apr 24
Under the deal, Genmab will gain global rights to ProfoundBio’s portfolio of next-generation ADCs which consists of three…
02 Apr 24
STRO-003, which is currently in the final stages of pre-clinical development, targets the ROR1 tumour antigen, which is…
Patient CarePharmaceuticals and MedicinesPartnerships and Licensing Agreements
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Developed by Eisai and Biogen, Leqembi is humanised IgG1 monoclonal antibody indicated as an AD therapy for patients…
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The approval is supported by the safety and efficacy data from the INNO2VATE programme and post-marketing safety data…
26 Mar 24
The acquisition is expected to advance Nuvation Bio as a late-stage, international oncology firm in which its current…
26 Mar 24
Through the deal, the American pharma major gains access to NX-13, Landos Biopharma’s flagship asset, which is being…
26 Mar 24
Q32 Bio to focus on advancement of bempikibart (ADX-914) in ongoing atopic dermatitis (AD) and alopecia areata (AA)…
26 Mar 24
Unprecedented relapse risk reduction observed in CHAMPION-NMOSD trial underscores how Ultomiris may redefine patient journey for rare neurological…
25 Mar 24
The approval was based on the findings from the confirmatory Phase 3 MIRASOL trial in which Elahere treatment…