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Everest Pharma Receives Approval for Clinical Trial Application of Zetomipzomib in China
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Everest Pharma Receives Approval for Clinical Trial Application of Zetomipzomib in China
13 December 2023
Everest Medicines, a biopharma company, announced that China's National Medical Products Administration has accepted their IND application for the drug candidate zetomipzomib in China.
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FDA Approves CARsgen's CT071 for Recurrent Multiple Myeloma and Primary Plasma Cell Leukemia Post-Therapy Failure
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FDA Approves CARsgen's CT071 for Recurrent Multiple Myeloma and Primary Plasma Cell Leukemia Post-Therapy Failure
13 December 2023
FDA Grants Approval for CARsgen's Experimental Treatment CT071 for Use in Cases of Recurrent Multiple Myeloma and Primary Plasma Cell Leukemia After Prior Therapies Fail.
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Brenig Therapeutics Reports BT-0267 LRRK2 Blocker Shows Improved Safety and Significant CSF Blood Levels at Parkinson's Symposium
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Brenig Therapeutics Reports BT-0267 LRRK2 Blocker Shows Improved Safety and Significant CSF Blood Levels at Parkinson's Symposium
12 December 2023
Brenig Therapeutics Reveals Enhanced Safety Metrics for its LRRK2 Blocker BT-0267 Featuring Notable CSF-to-Blood Concentration at the Parkinson's Disease Symposium.
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Merck Enhances Cancer Drug Offering By Securing Deal with Abbisko for Market Launch of Advanced Stage Drug, Pimicotinib
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Merck Enhances Cancer Drug Offering By Securing Deal with Abbisko for Market Launch of Advanced Stage Drug, Pimicotinib
12 December 2023
The prominent science and technology corporation, Merck, has declared a formal licensing contract with the Shanghai-based firm Abbisko Therapeutics Co. Ltd.
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Ascletis has commenced a stage three clinical evaluation for their acne medication, ASC40, also known as Denifanstat
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Ascletis has commenced a stage three clinical evaluation for their acne medication, ASC40, also known as Denifanstat
12 December 2023
Ascletis Pharma Inc. has declared the commencement of a pivotal Phase III clinical study for its fatty acid synthase inhibitor, ASC40 (Denifanstat) , aimed at addressing the therapeutic needs of individuals with moderate to severe acne vulgaris.
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Merus Showcases Preliminary Results for MCLA-129 at the 2023 ESMO Asia Congress
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Merus Showcases Preliminary Results for MCLA-129 at the 2023 ESMO Asia Congress
12 December 2023
Merus N.V. has revealed fresh interim clinical findings on their candidate molecule MCLA-129.
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European regulators have approved UCB's ZILBRYSQ® (zilucoplan) for adult generalized Myasthenia Gravis treatment
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European regulators have approved UCB's ZILBRYSQ® (zilucoplan) for adult generalized Myasthenia Gravis treatment
12 December 2023
UCB has received the green light from European regulators to market ZILBRYSQ[®] (zilucoplan) as a therapeutic option for generalized Myasthenia Gravis in adult patients.
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Sana Biotech's SC291, an off-the-shelf CAR T targeting CD19, undetected by immune system in initial clinical results
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Sana Biotech's SC291, an off-the-shelf CAR T targeting CD19, undetected by immune system in initial clinical results
12 December 2023
Sana Biotechnology Releases Initial Clinical Findings Demonstrating SC291, an Off-the-Shelf CAR T Treatment Targeting CD19, Remains Undetected by a Functional Immune System.
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Benitec Biopharma begins early trial dosing for BB-301, its genetic therapy for Oculopharyngeal Muscular Dystrophy
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Benitec Biopharma begins early trial dosing for BB-301, its genetic therapy for Oculopharyngeal Muscular Dystrophy
8 December 2023
Benitec Biopharma has reported initial dosing in an early-stage trial for its genetic treatment prospect, BB-301, aimed at tackling Oculopharyngeal Muscular Dystrophy.
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Ambrx Reports Advances in APEX-01, Phase 1/2 Trial of ARX517, a PSMA-Targeted ADC, in Hormone-Refractory Advanced Prostate Cancer
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Ambrx Reports Advances in APEX-01, Phase 1/2 Trial of ARX517, a PSMA-Targeted ADC, in Hormone-Refractory Advanced Prostate Cancer
8 December 2023
Ambrx Reports Progress on APEX-01 Trial, a Phase 1 / 2 Study Assessing Increasing Doses of ARX517, Its Own PSMA-Directed Antibody-Drug Conjugate, in Advanced Prostate Cancer Unresponsive to Hormonal Therapy.
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uniQure Reveals US FDA Approval for Clinical Trials of AMT-191, a Gene Therapy Candidate Targeting Fabry Disease
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uniQure Reveals US FDA Approval for Clinical Trials of AMT-191, a Gene Therapy Candidate Targeting Fabry Disease
8 December 2023
uniQure N.V., a leader in gene therapy, has announced FDA approval of its IND application for AMT-191 to treat severe medical conditions.
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BioVie Reveals Results of Phase 3 Study for NE3107 Treating Early to Mid-Stage Alzheimer's Patients
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BioVie Reveals Results of Phase 3 Study for NE3107 Treating Early to Mid-Stage Alzheimer's Patients
8 December 2023
BioVie Inc., a biopharmaceutical firm focusing on neurological, neurodegenerative, and severe liver diseases, reported positive initial results from its Phase 3 trial of NE3107 in mild to moderate Alzheimer’s patients.
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