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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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InnoCare Pharma announced FDA approval for its Bcl-2 inhibitor, ICP-248, to enter clinical trials
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InnoCare Pharma announced FDA approval for its Bcl-2 inhibitor, ICP-248, to enter clinical trials
22 January 2024
InnoCare Pharma has disclosed that the FDA has given approval to proceed with the clinical study for its BCL2 inhibitor, designated as ICP-248.
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AM-Pharma Begins Stage 2 Clinical Study on Ilofotase Alfa for Renal Injury Linked to Heart Surgery Procedures
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AM-Pharma Begins Stage 2 Clinical Study on Ilofotase Alfa for Renal Injury Linked to Heart Surgery Procedures
22 January 2024
AM-Pharma B.V. has started Phase 2 trials treating patients to test its enzyme, ilofotase alfa, for preventing kidney injury post-cardiac surgery.
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ExeVir Bio Announces Positive Virus Neutralization Data for XVR012 Against Emerging COVID-19 Omicron Variants
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ExeVir Bio Announces Positive Virus Neutralization Data for XVR012 Against Emerging COVID-19 Omicron Variants
18 January 2024
ExeVir Bio reports its antibodies effectively neutralize current COVID-19 Omicron strains.
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Encouraging Results in Initial Australian Trial for Androgenic Hair Loss Treatment
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Encouraging Results in Initial Australian Trial for Androgenic Hair Loss Treatment
18 January 2024
Hope Medicine Inc. announces successful completion of its Phase Ib "An Open-Label Study on Safety and Efficacy of HMI-115 in Androgenetic Alopecia over 24 Weeks," advancing its research milestones.
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Indapta Therapeutics Begins Treating Patients with IDP-023, a Non-Autologous NK Cell Cancer Therapy
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Indapta Therapeutics Begins Treating Patients with IDP-023, a Non-Autologous NK Cell Cancer Therapy
18 January 2024
Indapta Therapeutics Reveals Initial Treatment of Patients Using IDP-023, a Non-Self Derived NK Cell Treatment for Cancer Management.
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ARTBIO collaborates with PharmaLogic to distribute Lead-212 infused drug AB001 across NY and neighboring regions
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ARTBIO collaborates with PharmaLogic to distribute Lead-212 infused drug AB001 across NY and neighboring regions
18 January 2024
PharmaLogic Holdings Corp. has struck a deal with clinical stage innovator ARTBIO for the production of AB001, an experimental prostate cancer treatment using lead-212.
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FDA Approves Merck's KEYTRUDA with Chemoradiotherapy for Stage III-IVA Cervical Cancer Based on FIGO 2014 Criteria
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FDA Approves Merck's KEYTRUDA with Chemoradiotherapy for Stage III-IVA Cervical Cancer Based on FIGO 2014 Criteria
18 January 2024
FDA Sanctions Combination Use of Merck's KEYTRUDA (pembrolizumab) with Standard Chemoradiotherapy for Treating Stage III-IVA Cervical Cancer According to FIGO 2014 Criteria.
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