Recent blog posts
Brenig Therapeutics Reports BT-0267 LRRK2 Blocker Shows Improved Safety and Significant CSF Blood Levels at Parkinson's Symposium
Latest Hotspot
3 min read
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.
Read →
Merck Enhances Cancer Drug Offering By Securing Deal with Abbisko for Market Launch of Advanced Stage Drug, Pimicotinib
Latest Hotspot
3 min read
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.
Read →
Ascletis has commenced a stage three clinical evaluation for their acne medication, ASC40, also known as Denifanstat
Latest Hotspot
3 min read
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.
Read →
Merus Showcases Preliminary Results for MCLA-129 at the 2023 ESMO Asia Congress
Latest Hotspot
3 min read
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.
Read →
European regulators have approved UCB's ZILBRYSQ® (zilucoplan) for adult generalized Myasthenia Gravis treatment
Latest Hotspot
3 min read
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.
Read →
Sana Biotech's SC291, an off-the-shelf CAR T targeting CD19, undetected by immune system in initial clinical results
Latest Hotspot
3 min read
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.
Read →
Benitec Biopharma begins early trial dosing for BB-301, its genetic therapy for Oculopharyngeal Muscular Dystrophy
Latest Hotspot
3 min read
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.
Read →
Ambrx Reports Advances in APEX-01, Phase 1/2 Trial of ARX517, a PSMA-Targeted ADC, in Hormone-Refractory Advanced Prostate Cancer
Latest Hotspot
3 min read
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.
Read →
uniQure Reveals US FDA Approval for Clinical Trials of AMT-191, a Gene Therapy Candidate Targeting Fabry Disease
Latest Hotspot
3 min read
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.
Read →
BioVie Reveals Results of Phase 3 Study for NE3107 Treating Early to Mid-Stage Alzheimer's Patients
Latest Hotspot
3 min read
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.
Read →
Carisma Therapeutics Reveals Regulatory Green Light for Experimental HER2-Focused CAR-Monocyte Therapy CT-0525 by FDA
Latest Hotspot
3 min read
Carisma Therapeutics Reveals Regulatory Green Light for Experimental HER2-Focused CAR-Monocyte Therapy CT-0525 by FDA
8 December 2023
Carisma Therapeutics Inc. has confirmed that the U.S. Food and Drug Administration (FDA) has approved its Investigational New Drug (IND) application for their novel product, CT-0525.
Read →
Bio-Thera Solutions announced positive results from its Phase 3 trial of BAT2206, a potential Stelara® biosimilar
Latest Hotspot
3 min read
Bio-Thera Solutions announced positive results from its Phase 3 trial of BAT2206, a potential Stelara® biosimilar
8 December 2023
Bio-Thera Solutions has reported encouraging outcomes from its pivotal Phase 3 clinical trial involving BAT2206, a candidate biosimilar for Stelara®.
Read →