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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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Phase 3 FLOW Study: 1mg Ozempic® Reduces Kidney Disease Risk
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Phase 3 FLOW Study: 1mg Ozempic® Reduces Kidney Disease Risk
28 June 2024
The Phase 3 FLOW study presented at the 84th ADA Scientific Sessions showed a 1 mg dose of Ozempic® (semaglutide) injection decreased the risk of kidney disease-related events.
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Innovent Reveals Phase 3 Results of Mazdutide for Weight Control at ADA 84th Sessions
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Innovent Reveals Phase 3 Results of Mazdutide for Weight Control at ADA 84th Sessions
28 June 2024
Innovent Unveils Phase 3 Study Outcomes of Mazdutide for Weight Control at the ADA's 84th Scientific Sessions.
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EU Commission Approves Roche's OCREVUS: First Biannual Injection for Multiple Sclerosis
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EU Commission Approves Roche's OCREVUS: First Biannual Injection for Multiple Sclerosis
28 June 2024
The European Commission has approved Roche's OCREVUS for subcutaneous use, making it the first and only twice-yearly injection for relapsing and primary progressive multiple sclerosis.
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