Recent blog posts
Kairos Pharma Starts Phase 1 Trial of ENV105 Plus Osimertinib in EGFR-Related Lung Cancer Treatment
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Kairos Pharma Starts Phase 1 Trial of ENV105 Plus Osimertinib in EGFR-Related Lung Cancer Treatment
25 January 2024
Kairos Pharma, Ltd., specializing in developing new cancer treatments, has started a Phase 1 trial of its leading combination therapy. The study tests their drug ENV105 with osimertinib against non-small cell lung cancer.
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Adagene's ADG126 (muzastotug) and Pembrolizumab Show Superior Traits for Advanced MSS CRC Treatment
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Adagene's ADG126 (muzastotug) and Pembrolizumab Show Superior Traits for Advanced MSS CRC Treatment
25 January 2024
Adagene Inc., a leader in antibody therapeutics, shared research at the 2024 ASCO Symposium on Gastrointestinal Cancers in San Francisco.
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Regenxbio reports positive Phase II interim results for AAVIATE® with ABBV-RGX-314 administered via sclera to treat wet AMD
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Regenxbio reports positive Phase II interim results for AAVIATE® with ABBV-RGX-314 administered via sclera to treat wet AMD
24 January 2024
Regenxbio announces phase II aaviate ® The interim data of the trial were positive. Abbv-rgx-314 administered through sclera was used to treat wet AMD.
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Preliminary results from a Phase 1b trial indicate that Quemliclustat may improve survival in untreated advanced pancreatic cancer patients
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Preliminary results from a Phase 1b trial indicate that Quemliclustat may improve survival in untreated advanced pancreatic cancer patients
24 January 2024
Initial findings from a Phase 1b trial examining treatments with Quemliclustat suggest encouraging survival rates for patients with previously untreated advanced pancreatic cancer.
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Vertex Announces FDA Approval for CASGEVY™ (exagamglogene autotemcel) as Treatment for Blood Transfusion-Dependent Beta Thalassemia
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Vertex Announces FDA Approval for CASGEVY™ (exagamglogene autotemcel) as Treatment for Blood Transfusion-Dependent Beta Thalassemia
24 January 2024
Vertex Discloses Clearance by the US FDA for CASGEVY™ (exagamglogene autotemcel) as a Therapeutic Option for Beta Thalassemia Patients Requiring Regular Blood Transfusions.
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GALDERMA 2024: Phase III RelabotulinumtoxinA Trials Show Promising Results for Treating Facial Lines
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GALDERMA 2024: Phase III RelabotulinumtoxinA Trials Show Promising Results for Treating Facial Lines
24 January 2024
GALDERMA 2024: Phase III trials of RelabotulinumtoxinA show favorable outcomes and extended effectiveness in addressing both glabellar lines and lateral canthal lines at once.
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Aviceda Therapeutics Reports Promising Early Data from AVD-104 Study in Geographic Atrophy
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Aviceda Therapeutics Reports Promising Early Data from AVD-104 Study in Geographic Atrophy
24 January 2024
Aviceda Therapeutics Reveals Preliminary Results from Initial Segment of Phase 2/3 SIGLEC Study on AVD-104, Indicating Encouraging Safety Profile and Initial Efficacy Signals in Individuals with Geographic Atrophy.
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Aruna Bio's AB126 exosome therapy has gained FDA approval for its IND application
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Aruna Bio's AB126 exosome therapy has gained FDA approval for its IND application
24 January 2024
Aruna Bio has received FDA approval for its investigational new drug (IND) application, allowing AB126, its pioneering exosome therapy.
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Sarepta's EMERGENE Phase 3 Trial on SRP-9003 for LGMD 2E/R4 Begins Participant Enrollment
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Sarepta's EMERGENE Phase 3 Trial on SRP-9003 for LGMD 2E/R4 Begins Participant Enrollment
22 January 2024
Sarepta Therapeutics Launches Participant Selection for Phase 3 Trial, EMERGENE, Investigating SRP-9003 in Limb-Girdle Muscular Dystrophy 2E/R4 Treatment.
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CARsgen's CT011 Granted NMPA Clearance for Phase IIIa Liver Cancer Trial
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CARsgen's CT011 Granted NMPA Clearance for Phase IIIa Liver Cancer Trial
22 January 2024
CARsgen's candidate, CT011, has secured authorization from the NMPA to proceed with trials for GPC3-positive Ⅲa hepatocellular carcinoma patients with a significant risk of recurrence post-surgery.
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Roche's Tecentriq® with ENHANZE® Tech Gets EU Clearance for Subcutaneous Use in Cancer Therapy
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Roche's Tecentriq® with ENHANZE® Tech Gets EU Clearance for Subcutaneous Use in Cancer Therapy
22 January 2024
Halozyme Reports Roche Granted EU Clearance for Subcutaneous Form of Tecentriq® with ENHANZE® Technology, Marking a Breakthrough in the Delivery of Immunotherapies Across Various Cancers.
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Chipscreen NewWay Begins Phase 1 Trial of NWY001 for Cancer Immunotherapy
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Chipscreen NewWay Begins Phase 1 Trial of NWY001 for Cancer Immunotherapy
22 January 2024
Chipscreen NewWay Initiates Phase 1 Study: Administers Initial Dose of Innovative Dual-Targeting Antibody NWY001 for Advancing Cancer Immune Therapy in Individuals with Progressive Solid Cancers.
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