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Boehringer Ingelheim's Adalimumab-adbm is available at low wholesale acquisition cost
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Boehringer Ingelheim's Adalimumab-adbm is available at low wholesale acquisition cost
12 October 2023
Boehringer Ingelheim revealed that their interchangeable* biosimilar to Humira®, known as Adalimumab-adbm injection, is now available at a low wholesale acquisition cost.
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Caliway's CBL-514 demonstrated superior effectiveness compared to Liposuction
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Caliway's CBL-514 demonstrated superior effectiveness compared to Liposuction
12 October 2023
Caliway Biopharmaceuticals announced successful primary and secondary endpoints of the phase 2 stage 2 trial for CBL-0202, outperforming placebo in ITT and PP groups.
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Rocket Pharmaceuticals reveals that FDA Acceptance of BLA for RP-L201
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Rocket Pharmaceuticals reveals that FDA Acceptance of BLA for RP-L201
12 October 2023
The U.S. FDA has granted Priority Review to Rocket Pharmaceuticals, Inc. for their late-stage gene therapy, RP-L201 (marnetegragene autotemcel).
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Lassen Therapeutics revealed preclinical findings related to LASN01, an Anti-IL-11 Receptor Antibody for Thyroid Eye Disease
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Lassen Therapeutics revealed preclinical findings related to LASN01, an Anti-IL-11 Receptor Antibody for Thyroid Eye Disease
12 October 2023
Presenting new preclinical data on LASN01 for treating TED, Lassen Therapeutics, a biotechnology firm engaged in clinical stages, is pioneering unique antibody therapeutics.
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Kashiv BioSciences Administers First Patient in Phase III Clinical Trial for ADL018
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Kashiv BioSciences Administers First Patient in Phase III Clinical Trial for ADL018
12 October 2023
Kashiv BioSciences, LLC declared the start of enrollment for their Phase III clinical trial initiating with their first patient for their biosimilar candidate, ADL018, a potential alternative to XOLAIR®.
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Nexcella reveals clinical data from NXC-201 study in Multiple Myeloma
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Nexcella reveals clinical data from NXC-201 study in Multiple Myeloma
12 October 2023
Nexcella Inc. revealed updates from its ongoing Phase 1b/2 NEXICART-1 trial on its proprietary BCMA-targeted CAR T cell treatment, NXC-201.
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A Phase III trial investigating Novartis' experimental drug, Iptacopan, displayed findings in IgAN patients
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A Phase III trial investigating Novartis' experimental drug, Iptacopan, displayed findings in IgAN patients
12 October 2023
Novartis reported promising initial results from a 9-month interim assessment of the Phase III APPLAUSE-IgAN trial. The experimental factor B inhibitor, iptacopan, showed superior effectiveness in reducing proteinuria compared to placebo.
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FDA Grants Authorization for Biogen's TOFIDENCE™ (tocilizumab-bavi), a Biosimilar Linked to ACTEMRA®
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FDA Grants Authorization for Biogen's TOFIDENCE™ (tocilizumab-bavi), a Biosimilar Linked to ACTEMRA®
12 October 2023
Biogen Inc. disclosed that the U.S. FDA provided their endorsement for TOFIDENCE (tocilizumab-bavi) in an intravenous format, a biosimilar monoclonal antibody that references ACTEMRA.
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AbbVie shares findings from its Phase 3 trial involving Venetoclax for individuals with Multiple Myeloma
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AbbVie shares findings from its Phase 3 trial involving Venetoclax for individuals with Multiple Myeloma
12 October 2023
AbbVie shared Phase 3 CANOVA trial results for the VenDex combo in treating relapsed or resistant multiple myeloma in patients with two or more prior treatments.
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JCR Pharmaceuticals Reveals Findings from Phase I/II Research of JR-171 in people with Mucopolysaccharidosis Type I
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JCR Pharmaceuticals Reveals Findings from Phase I/II Research of JR-171 in people with Mucopolysaccharidosis Type I
12 October 2023
JCR Pharmaceuticals Co., Ltd. has disclosed critical findings from the midway 52-week data of its global research phase I/II involving JR-171 (lepunafusp alfa) in patients diagnosed with mucopolysaccharidosis type I.
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Geron Reports Validation by EMA of Marketing Approval Submission for Imetelstat
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Geron Reports Validation by EMA of Marketing Approval Submission for Imetelstat
11 October 2023
Geron Corporation declared that the Marketing Authorization Application concerning imetelstat-a novel experimental telomerase inhibitor-has been accepted and validated by the EMA.
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FDA approves priority review of Odronextamab BLA for relapsed/refractory follicular and diffuse large B-cell lymphoma
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FDA approves priority review of Odronextamab BLA for relapsed/refractory follicular and diffuse large B-cell lymphoma
11 October 2023
FDA accepts Priority Review of Odronextamab BLA for Relapsed/Refractory Follicular Lymphoma and Diffuse Large B-cell Lymphoma.
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