Recent blog posts
Shanghai Huaota Biopharmaceutical's IL-36R monoclonal antibody, HB0034, has been granted Orphan Drug Designation by the FDA for the treatment of generalized pustular psoriasis
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Shanghai Huaota Biopharmaceutical's IL-36R monoclonal antibody, HB0034, has been granted Orphan Drug Designation by the FDA for the treatment of generalized pustular psoriasis
24 October 2023
Shanghai Huaota Biopharmaceutical's HB0034 anti-IL-36R monoclonal antibody injection was granted orphan drug designation by the U.S. FDA for the treatment of generalized pustular psoriasis (GPP).
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Shanghai Junshi Biosciences' anti-PD-1 monoclonal antibody, Toripalimab, announces Phase 3 trial data for the treatment of small-cell lung cancer
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Shanghai Junshi Biosciences' anti-PD-1 monoclonal antibody, Toripalimab, announces Phase 3 trial data for the treatment of small-cell lung cancer
24 October 2023
The 2023 ESMO congress selected Shanghai Junshi Biosciences' phase III trial, EXTENTORCH, on anti-PD-1 monoclonal antibody toripalimab for the LBA.
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CStone Pharmaceuticals releases Phase 3 GEMSTONE-303 clinical trial data of anti-PD-L1 monoclonal antibody sugemalimab, for the treatment of gastric cancer
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CStone Pharmaceuticals releases Phase 3 GEMSTONE-303 clinical trial data of anti-PD-L1 monoclonal antibody sugemalimab, for the treatment of gastric cancer
24 October 2023
The GEMSTONE-303 Phase III trial of CStone Pharmaceuticals' sugemalimab was selected for an LBA report at the 2023 ESMO conference.
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Sanofi's phase 3 clinical trial data for teplizumab published in NEJM, for the treatment of type 1 diabetes
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Sanofi's phase 3 clinical trial data for teplizumab published in NEJM, for the treatment of type 1 diabetes
23 October 2023
Recently, Sanofi announced the latest data from the Phase 3 clinical trial named PROTECT for Tzield (teplizumab).
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AstraZeneca's C5 complement inhibitor, Eculizumab, has been approved in China for a new indication: the treatment of Neuromyelitis Optica Spectrum Disorder
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AstraZeneca's C5 complement inhibitor, Eculizumab, has been approved in China for a new indication: the treatment of Neuromyelitis Optica Spectrum Disorder
23 October 2023
Recently, AstraZeneca announced that the National Medical Products Administration (NMPA) of China has approved C5 complement inhibitor Eculizumab for the treatment of adults.
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UCB's innovative therapy, IL-17A/F inhibitor bimekizumab, has been approved by the FDA for the treatment of plaque psoriasis
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UCB's innovative therapy, IL-17A/F inhibitor bimekizumab, has been approved by the FDA for the treatment of plaque psoriasis
23 October 2023
Recently, UCB announced that the FDA has approved Bimzelx(bimekizumab) for the treatment of moderate to severe plaque psoriasis in adult patients who are candidates for systemic treatment or phototherapy.
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Angany reveals initial human clinical trial for ANG-101, a potential vaccine for feline allergies
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Angany reveals initial human clinical trial for ANG-101, a potential vaccine for feline allergies
19 October 2023
Angany Inc.. has revealed that it has obtained approval from MHRA to carry out the initial clinical trial of its vaccine candidate ANG-101 aimed at combating allergies in humans to cats.
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KEYTRUDA® (pembrolizumab), a Merck product, met its main objective of disease-free survival (DFS) in specific patients with Muscle-Invasive Urothelial Carcinoma post-surgery
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KEYTRUDA® (pembrolizumab), a Merck product, met its main objective of disease-free survival (DFS) in specific patients with Muscle-Invasive Urothelial Carcinoma post-surgery
19 October 2023
Merck recently proclaimed that the Phase 3 AMBASSADOR study assessing KEYTRUDA, an anti-PD-1 treatment developed by Merck.
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Stage III research on survodutide for individuals struggling with obesity and overweight, including those with or without diabetes, heart disease, and persistent kidney disorders
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Stage III research on survodutide for individuals struggling with obesity and overweight, including those with or without diabetes, heart disease, and persistent kidney disorders
19 October 2023
In conjunction with Zealand Pharma A/S, Boehringer Ingelheim has initiated three Phase III research investigations for survodutide (also known as BI 456906)
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First patient given TN-201 in Tenaya Therapeutics' MyPeak-1™ Phase 1b trial for MYBPC3-related Hypertrophic Cardiomyopathy
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First patient given TN-201 in Tenaya Therapeutics' MyPeak-1™ Phase 1b trial for MYBPC3-related Hypertrophic Cardiomyopathy
19 October 2023
First patient administered by Tenaya Therapeutics in MyPeak-1™ Phase 1b Clinical Trial for TN-201 treatment to address MYBPC3-Associated Hypertrophic Cardiomyopathy.
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Oncternal Therapeutics begins phase 1/2 trial of ONCT-534, a dual-action AR inhibitor, on metastatic castration-resistant prostate cancer patients
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Oncternal Therapeutics begins phase 1/2 trial of ONCT-534, a dual-action AR inhibitor, on metastatic castration-resistant prostate cancer patients
18 October 2023
Oncternal Therapeutics starts administrating the first dose in phase 1/2 trial of ONCT-534, a dual-action AR inhibitor, for metastatic castration-resistant prostate cancer patients.
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Janssen applies to European Medicines Agency for approval to use RYBREVANT (amivantamab) plus chemotherapy for newly diagnosed advanced NSCLC patients with EGFR Exon 20 Insertion Mutations
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Janssen applies to European Medicines Agency for approval to use RYBREVANT (amivantamab) plus chemotherapy for newly diagnosed advanced NSCLC patients with EGFR Exon 20 Insertion Mutations
18 October 2023
Janssen applies to the European Medicines Agency, seeking approval for using RYBREVANT (amivantamab) combined with chemotherapy to treat adults initially diagnosed with late-stage Non-Small Cell Lung Cancer with proficient EGFR Exon 20 Insertion Mutations.
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