Recent blog posts
Meitheal Pharmaceuticals Boosts Biologics Range through Exclusive Licensing Deal for YUSIMRY®, a Humira® Biosimilar
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Meitheal Pharmaceuticals Boosts Biologics Range through Exclusive Licensing Deal for YUSIMRY®, a Humira® Biosimilar
2 July 2024
Meitheal Pharmaceuticals has obtained exclusive U.S. commercial rights for YUSIMRY, a biosimilar to Humira.
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CASI Pharmaceuticals Proposes IND for CID-103 and Considers Sale of China Operations
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CASI Pharmaceuticals Proposes IND for CID-103 and Considers Sale of China Operations
2 July 2024
CASI Pharmaceuticals Plans IND Submission for CID-103 in Antibody-Mediated Rejection and Receives Non-Binding Offer to Acquire Its China Operations.
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FDA Approves EPKINLY® for Relapsed/Refractory Follicular Lymphoma
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FDA Approves EPKINLY® for Relapsed/Refractory Follicular Lymphoma
2 July 2024
The U.S. FDA has granted approval to EPKINLY® (epcoritamab-bysp) for individuals with relapse or refractory (R/R) follicular lymphoma (FL).
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Lyell Immunopharma Reports Phase 1 Dose-dependent Efficacy of ROR1 CAR-T Therapy LYL797, Boosted by Anti-exhaustion Tech
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Lyell Immunopharma Reports Phase 1 Dose-dependent Efficacy of ROR1 CAR-T Therapy LYL797, Boosted by Anti-exhaustion Tech
2 July 2024
Lyell Immunopharma Announces Phase 1 Results for ROR1-targeted CAR-T Candidate, LYL797, Showing Dose-dependent Efficacy Enhanced by Anti-exhaustion Technology.
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Simcere Zaiming Announces NMPA Approval of Cetuximab Beta in China
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Simcere Zaiming Announces NMPA Approval of Cetuximab Beta in China
2 July 2024
Simcere Zaiming, announced that their new anti-EGFR antibody treatment, Enlituo®, has been officially approved for sale by the China National Medical Administration.
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Encouraging Phase I Results for HUADONG MEDICINE'S Oral GLP-1 Receptor Agonist HDM1002
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Encouraging Phase I Results for HUADONG MEDICINE'S Oral GLP-1 Receptor Agonist HDM1002
1 July 2024
HUADONG MEDICINE Reports Encouraging Phase I Outcomes for New Oral GLP-1 Receptor Agonist HDM1002.
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Star Therapeutics Reveals VGA039 Clinical Results for VWD Treatment
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Star Therapeutics Reveals VGA039 Clinical Results for VWD Treatment
1 July 2024
Star Therapeutics Unveils Clinical Findings on VGA039, an Injectable Therapy for Von Willebrand Disease (VWD).
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Arrowhead Advances RNAi Therapy Plozasiran to Phase 3 CAPITAN Trial in Cardiovascular Study
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Arrowhead Advances RNAi Therapy Plozasiran to Phase 3 CAPITAN Trial in Cardiovascular Study
1 July 2024
Arrowhead Pharmaceuticals to Progress RNAi Therapy Plozasiran into Phase 3 CAPITAN Trial for Cardiovascular Results.
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Early Phase 1 Results of WTX-330 on Advanced Solid Tumors and Non-Hodgkin Lymphoma Presented by Werewolf Therapeutics
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Early Phase 1 Results of WTX-330 on Advanced Solid Tumors and Non-Hodgkin Lymphoma Presented by Werewolf Therapeutics
1 July 2024
Werewolf Therapeutics Presents Early Safety and Effectiveness Results from Phase 1 Study of WTX-330 in Patients with Advanced Solid Tumors or Non-Hodgkin Lymphoma.
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EZHARMIA® Approved in Japan as First Dual EZH1/EZH2 Inhibitor for Peripheral T-Cell Lymphoma Therapy
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EZHARMIA® Approved in Japan as First Dual EZH1/EZH2 Inhibitor for Peripheral T-Cell Lymphoma Therapy
1 July 2024
EZHARMIA® Receives Approval in Japan as the First Dual EZH1 and EZH2 Blocker for Peripheral T-Cell Lymphoma Therapy.
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vTv Therapeutics Begins Key CATT1 Study Enrollment for Cadisegliatin in Type 1 Diabetes
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vTv Therapeutics Begins Key CATT1 Study Enrollment for Cadisegliatin in Type 1 Diabetes
1 July 2024
vTv Therapeutics Announces Enrollment of First Participant in CATT1 Key Study for Cadisegliatin in Type 1 Diabetes.
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TiumBio Reveals Promising Early Data for Hemophilia Candidate TU7710 at ISTH 2024
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TiumBio Reveals Promising Early Data for Hemophilia Candidate TU7710 at ISTH 2024
28 June 2024
TiumBio Unveils Promising Initial Clinical Data for TU7710, Its Hemophilia Therapy Candidate, at ISTH 2024.
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