Recent blog posts
Sandoz Obtains US Health Regulator's Green Light for Unique Denosumab Bioequivalents
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Sandoz Obtains US Health Regulator's Green Light for Unique Denosumab Bioequivalents
7 March 2024
Sandoz announced that its products Wyost® and Jubbonti®, both containing denosumab-bbdz, have been approved by the US FDA.
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Innate Pharma Reveals Early Research on Nectin-4 Targeting Agent IPH45 at 2024 AACR Event
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Innate Pharma Reveals Early Research on Nectin-4 Targeting Agent IPH45 at 2024 AACR Event
7 March 2024
Innate Pharma SA has declared that its pioneering research on the preclinical compound IPH45, a unique Antibody Drug Conjugate that targets Nectin-4 by inhibiting topoisomerase I.
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Pfizer's Clinical Advancements with Drug PF-08046052 Reported by LAVA
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Pfizer's Clinical Advancements with Drug PF-08046052 Reported by LAVA
7 March 2024
LAVA has reported progress in clinical phase achievements by Pfizer with the drug PF-08046052, previously known as SGN-EGFRd2 or LAVA-1223.
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First Patient Treated in IPH6501 Trial for Relapsed/Refractory B-Cell NHL
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First Patient Treated in IPH6501 Trial for Relapsed/Refractory B-Cell NHL
7 March 2024
Inborn Therapeutics: Initial Participant Treated in Early-to-Mid Stage Trial of IPH6501 for Recurrent or Resistant B-Cell Non-Hodgkin Lymphoma.
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Promising Early Results for BI-1206 in Chinese Non-Hodgkin's Lymphoma Study by CASI Pharma
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Promising Early Results for BI-1206 in Chinese Non-Hodgkin's Lymphoma Study by CASI Pharma
7 March 2024
CASI Pharma Announces Encouraging Early Results for BI-1206 in Managing Persistent Forms of Non-Hodgkin’s Lymphoma in Chinese Study.
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Nektar Launches Phase 2b Trial for Severe Alopecia Areata Treatment
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Nektar Launches Phase 2b Trial for Severe Alopecia Areata Treatment
7 March 2024
Nektar Therapeutics has launched a Phase 2b trial to assess Rezpegaldesleukin in individuals with severe forms of Alopecia Areata.
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Ankrya Therapeutics Begins Human Trials for ANK-101, a New Cancer Immunotherapy
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Ankrya Therapeutics Begins Human Trials for ANK-101, a New Cancer Immunotherapy
7 March 2024
Ankyra Therapeutics has commenced dosing in its initial human trial phase, assessing the effectiveness of ANK-101, a novel anchored immunotherapy, targeting a range of solid cancers.
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Novartis Reveals Zolgensma Data Improves Motor Skills in Older SMA Children
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3 min read
Novartis Reveals Zolgensma Data Improves Motor Skills in Older SMA Children
6 March 2024
Novartis unveils fresh insights into Zolgensma's safety and performance, highlighting sustained and enhanced motor skills in SMA-affected children who are larger and older.
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Cullinan Oncology's CLN-619: FDA Greenlights Initial Trials for Novel MICA/B Antibody in Advanced Multiple Myeloma
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3 min read
Cullinan Oncology's CLN-619: FDA Greenlights Initial Trials for Novel MICA/B Antibody in Advanced Multiple Myeloma
6 March 2024
Cullinan Oncology Reveals FDA Approval for Initial Trials of Unique MICA/B Antibody, CLN-619, Targeting Advanced Multiple Myeloma Cases.
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FDA Approves IND Submission for Atara's ATA3219, an Off-the-Shelf CAR T Therapy for Lupus Nephritis
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FDA Approves IND Submission for Atara's ATA3219, an Off-the-Shelf CAR T Therapy for Lupus Nephritis
6 March 2024
ATA3219, an off-the-shelf CAR T treatment by Atara Biotherapeutics, gets green light from the FDA for its IND submission targeting Lupus Nephritis.
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UK Regulators Greenlight Ariceum's Early Trial for I-123 Tagged PARP Blocker in Recurrent Glioblastoma Patients
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UK Regulators Greenlight Ariceum's Early Trial for I-123 Tagged PARP Blocker in Recurrent Glioblastoma Patients
6 March 2024
UK regulators have approved Ariceum Therapeutics to initiate an early-stage trial with its innovative I-123 tagged PARP blocker for individuals experiencing repeated glioblastoma.
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Jacobio Gains U.S. Approval for IND Status of New P53 Y220C Stimulant JAB-30300
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Jacobio Gains U.S. Approval for IND Status of New P53 Y220C Stimulant JAB-30300
6 March 2024
Jacobio Pharmaceuticals Secures U.S. Go-Ahead for Experimental P53 Y220C Stimulant JAB-30300 under Investigational New Drug Status.
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