Recent blog posts
Tvardi Therapeutics Announces Phase 2 Trial of STAT3 Inhibitor TTI-101 for Idiopathic Pulmonary Fibrosis
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Tvardi Therapeutics Announces Phase 2 Trial of STAT3 Inhibitor TTI-101 for Idiopathic Pulmonary Fibrosis
4 September 2023
Tvardi Therapeutics, Inc., a clinical-stage biopharmaceutical company specializing in the development of STAT3 inhibitors, has initiated dosing of the first patients in its ongoing REVERTIPF trial.
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Genentech's Alecensa has achieved remarkable Phase III outcomes for individuals diagnosed with early-stage lung cancer that is positive for the ALK mutation
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Genentech's Alecensa has achieved remarkable Phase III outcomes for individuals diagnosed with early-stage lung cancer that is positive for the ALK mutation
4 September 2023
Genentech announced today that the Phase III ALINA study assessing Alecensa® (alectinib) has achieved its primary endpoint of disease-free survival (DFS) during a pre-determined interim analysis.
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The U.S. has granted IND approval to HBM9033, the initial ADC project for solid tumors by Harbour BioMed
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The U.S. has granted IND approval to HBM9033, the initial ADC project for solid tumors by Harbour BioMed
4 September 2023
Harbour BioMed declared that the U.S. FDA has given the go-ahead for the IND application, permitting the initiation of clinical studies for its inaugural Antibody Drug Conjugate (ADC) project, HBM9033.
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The FDA has given its approval to Mallinckrodt for marketing Dextroamphetamine for managing Attention Deficit/Hyperactivity Disorder (ADHD)
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The FDA has given its approval to Mallinckrodt for marketing Dextroamphetamine for managing Attention Deficit/Hyperactivity Disorder (ADHD)
4 September 2023
The FDA has given Mallinckrodt the green light to market Lisdexamfetamine Dimesylate Capsules, a product intended to mitigate Attention-Deficit/Hyperactivity Disorder (ADHD).
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AstraZeneca's BTK Inhibitor Acalabrutinib gets Approval for New Indications in China
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AstraZeneca's BTK Inhibitor Acalabrutinib gets Approval for New Indications in China
3 September 2023
On September 1, 2023, the NMPA officially approved a new indication for AstraZeneca's blood cancer product, Acalabrutinib, for adults with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL).
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Mabspace Biosciences initiates global Phase III clinical trials for CLDN 18.2 monoclonal antibody TST001
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Mabspace Biosciences initiates global Phase III clinical trials for CLDN 18.2 monoclonal antibody TST001
3 September 2023
On September 1, 2023, Mabspace Biosciences registered an international multicenter Phase III clinical trial on the Drug Clinical Trial Registration and Information Publicity Platform.
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Zai Lab's new drug Maqituxi Monoclonal Antibody Injection targeting HER2 has been approved in China
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Zai Lab's new drug Maqituxi Monoclonal Antibody Injection targeting HER2 has been approved in China
3 September 2023
Margetuximab is an Fc-optimized monoclonal antibody acting on HER2, which was introduced by Zai Lab from MacroGenics.
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Sirnaomics announced positive results from phase 1 clinical trials of siRNA therapy STP707
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Sirnaomics announced positive results from phase 1 clinical trials of siRNA therapy STP707
3 September 2023
On August 31, 2023, Sirnaomics announced positive results from Phase 1 clinical trials of its RNAi therapy STP707 for treating various solid tumors.
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Neurocrine's VMAT2 inhibitor Valbenazine achieves endpoint in Phase 3 clinical trial
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Neurocrine's VMAT2 inhibitor Valbenazine achieves endpoint in Phase 3 clinical trial
3 September 2023
Recently, Neurocrine Biosciences announced new data for the VMAT2 inhibitor drug Ingrezza (valbenazine) capsules, including preliminary results from the Phase III KINECT-HD clinical trial.
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Bristol-Myers Squibb’s mavacamten has announced long-term follow-up data from two phase 3 trials for the treatment of hypertrophic cardiomyopathy
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Bristol-Myers Squibb’s mavacamten has announced long-term follow-up data from two phase 3 trials for the treatment of hypertrophic cardiomyopathy
2 September 2023
Recently, Bristol Myers Squibb has announced the latest long-term follow-up results of two Phase 3 studies that assessed the treatment efficacy of Camzyos (mavacamten).
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Roche's PD-L1 monoclonal antibody, Atezolizumab subcutaneous formulation, has received approval for marketing by the UK's MHRA
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Roche's PD-L1 monoclonal antibody, Atezolizumab subcutaneous formulation, has received approval for marketing by the UK's MHRA
2 September 2023
Recently, Roche announced that its PD-L1 targeted antibody, Tecentriq(atezolizumab), has been approved for marketing in the UK by the Medicines and Healthcare products Regulatory Agency (MHRA).
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The Phase 1 clinical trial for the KRAS G12D inhibitor MRTX1133, developed by Mirati, has been launched
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The Phase 1 clinical trial for the KRAS G12D inhibitor MRTX1133, developed by Mirati, has been launched
2 September 2023
the combined therapy of KRAS G12D inhibitor MRTX1133 and immune checkpoint inhibitors can cause sustained tumor elimination and significantly improve the survival outcomes in mice.
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