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Skyline Therapeutics Receives FDA Clearance of IND for SKG0106, a Novel Intravitreally Delivered AAV Gene Therapy Candidate for Neovascular Age-related Macular Degeneration

Skyline Therapeutics Receives FDA Clearance of IND for SKG0106, a Novel Intravitreally Delivered AAV Gene Therapy Candidate for Neovascular Age-related Macular Degeneration On July 3, 2023, Skyline Therapeutics, an innovation-driven gene therapy company committed to developing unique and novel solutions for rare and severe diseases, announced that the U.S. Food and Drug Administration (FDA) has ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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National Cancer Center Announces Recipients of 2023-24 Research Fellowship Awards

National Cancer Center Announces Recipients of 2023-24 Research Fellowship Awards The National Cancer Center is pleased to announce the recipients of its 2023-24 research grant awards, which support research fellows pursuing promising and innovative cancer research. This year’s class of 15 recipients—six first-time awards and nine renewals—hail from China, India, Bangladesh, Italy, Mexico, South..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Aquestive Therapeutics Provides Business Update and Announces Chief Medical Officer Appointment

Aquestive Therapeutics Provides Business Update and Announces Chief Medical Officer Appointment &nbsp Aquestive Therapeutics, a pharmaceutical company specializing in advancing medicines to improve patients' lives, has recently submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for their product Libervant™ (diazepam) Buccal Film. The NDA is specifically for the..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Corvus Pharmaceuticals Presents New Ciforadenant Preclinical Data at the 2nd JCA-AACR Precision Cancer Medicine International Conference

Corvus Pharmaceuticals, a clinical-stage biopharmaceutical company, presented new preclinical data for ciforadenant at the 2nd JCA-AACR Precision Cancer Medicine International Conference. The data highlights ciforadenant's mechanism of action and its synergy with immune checkpoint inhibitors. Corvus is currently conducting a Phase 1b/2 clinical trial to evaluate ciforadenant as a potential first..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Positive Interim Updates from ReSPECT™ Clinical Trials Presented at SNMMI Annual Meeting

Plus Therapeutics, a clinical-stage pharmaceutical company, announced positive interim updates from its ReSPECT™ clinical trials at the Society of Nuclear Medicine & Molecular Imaging (SNMMI) Annual Meeting. The ReSPECT-GBM Phase 1 trial showed safety and overall survival correlation with absorbed radiation dose in recurrent glioblastoma patients. The ReSPECT-LM Phase 1/Part A trial demonstrated..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Harbour BioMed Announces Biologics License Application Acceptance of Batoclimab for Treatment of Generalized Myasthenia Gravis by NMPA

Harbour BioMed, a global biopharmaceutical company, has announced that the National Medical Products Administration (NMPA) of China has accepted its Biologics License Application (BLA) for batoclimab in the treatment of generalized myasthenia gravis (gMG). This marks the first BLA accepted by NMPA since Harbour BioMed's establishment. Batoclimab is an innovative therapy targeting anti-FcRn treat..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Microbot Medical Successfully Completes Pre-Clinical Study with LIBERTY Robotic Surgical System

Microbot Medical Successfully Completes an Extensive Pre-Clinical Study Performed in the US Microbot Medical Inc. (Nasdaq: MBOT) announced the successful completion of an extended pre-clinical study conducted by global key opinion leaders ("KOLs") and executives from the medical industry. The study took place over two days at a research lab in New York. A team of interventional radiologists util..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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SK Bioscience and Sanofi Announce Positive Results from Phase II Study of 21-Valent Pneumococcal Conjugate Vaccine Candidate

SK bioscience and Sanofi have announced positive results from the Phase II study of their 21-valent pneumococcal conjugate vaccine candidate, GBP410 (also known as SP0202). The vaccine demonstrated positive safety and immunogenicity data in infants. The companies plan to start Phase III trials in the first half of 2024. The Phase II clinical trial evaluated the safety and immunogenicity of GBP41..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Osemitamab (TST001) plus CAPOX as the First-Line Treatment of Advanced G/GEJ Cancer – Updated Efficacy Data per Claudin 18.2 Expression Level from Study TranStar102/TST001-1002-Cohort C

Transcenta Holding Limited ("Transcenta") presented the progression-free survival (PFS) data from a Phase I/II study of Osemitamab (TST001) plus Capecitabine and Oxaliplatin (CAPOX) as the first-line treatment for advanced gastric/gastroesophageal junction (G/GEJ) cancer. The study showed that the addition of Osemitamab to chemotherapy provided benefit to patients with CLDN18.2 positive tumors, ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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FSD Pharma Inc. Announces Results of Annual General and Special Meeting of Shareholders

FSD Pharma Inc. Announces Results of Annual General and Special Meeting of Shareholders FSD Pharma Inc., a biopharmaceutical company dedicated to innovative solutions for neurodegenerative, inflammatory, and metabolic disorders, has released the outcomes of its annual general and special meeting of shareholders held on June 29, 2023. During the meeting, there were 148 shareholders present or rep..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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