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Bolt Biotherapeutics Starts Phase 2 Trial Enrollment for BDC-1001 in HER2+ Breast Cancer Patients Pre-Treated with Enhertu
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Bolt Biotherapeutics Starts Phase 2 Trial Enrollment for BDC-1001 in HER2+ Breast Cancer Patients Pre-Treated with Enhertu
13 December 2023
Bolt Biotherapeutics Commences Phase 2 Clinical Trial Enrollment for BDC-1001 in HER2-Positive Breast Cancer Subjects Previously Administered Enhertu.
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Coherus Presents Casdozokitug Early Results at ESMO 2023 Immuno-Oncology
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Coherus Presents Casdozokitug Early Results at ESMO 2023 Immuno-Oncology
13 December 2023
Coherus Showcases Early-Stage Study Results for its Novel IL-27-Specific Antibody, Casdozokitug, at ESMO's 2023 Immuno-Oncology Meeting.
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Qilu Pharma's Phase 2 trial data shows 45.8% response rate for Iparomlimab in solid cancers at ESMO Asia
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Qilu Pharma's Phase 2 trial data shows 45.8% response rate for Iparomlimab in solid cancers at ESMO Asia
13 December 2023
Qilu Pharma Reports Data on Phase 2 Trial of Iparomlimab in Treating Progressive Solid Cancers, Reveals 45.8% Objective Response Rate at ESMO Asia Conference.
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First ANCA-related vasculitis patient with rapid kidney involvement joins and receives treatment in Alentis Therapeutics’ Phase II Lixudebart (ALE.F02) trial
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First ANCA-related vasculitis patient with rapid kidney involvement joins and receives treatment in Alentis Therapeutics’ Phase II Lixudebart (ALE.F02) trial
13 December 2023
First patient with swiftly advancing ANCA-Related Vasculitis and kidney inflammation enrolled and treated in Phase II study of new drug Lixudebart (ALE.F02) by Alentis Therapeutics.
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GT Biopharma Reveals IND Filing for Their New Drug GTB-3650 Targeting CD33+ Leukemia Therapy
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GT Biopharma Reveals IND Filing for Their New Drug GTB-3650 Targeting CD33+ Leukemia Therapy
13 December 2023
GT Biopharma, Inc., a clinical-stage immuno-oncology company, is committed to developing innovative therapies using its proprietary TriKE® NK cell technology. The firm recently announced it filed an IND application with the US FDA for its new drug, GTB-3650.
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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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