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UAE, Saudi Arabia Serve as Gateway to International Markets for Biopharma

UAE and Saudi Arabia: Gateways to International Biopharma Markets Biopharmaceutical companies like Sanofi, AbbVie, and Virax Biolabs are capitalizing on lucrative business opportunities in the Middle East, particularly in the United Arab Emirates (UAE) and Saudi Arabia. These countries have become attractive markets for cutting-edge therapies, driven by their growing populations with a rising in..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 13.
  • textsms

Title: "Seven Biotechs and Biopharmas Post Sizable IPOs in 2023 Despite Industry Drought"

Despite the challenging economic climate, the life science industry has witnessed a total of seven significant IPOs in 2023. However, when compared to previous years, it is clear that there is still a drought in IPO activity within the industry. In 2022, there were only 47 biotech IPOs, raising approximately $4 billion. This marks a significant decrease from 2021, which saw 152 offerings raising..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 13.
  • textsms

MaxCyte and Vittoria Biotherapeutics Sign Strategic Platform License to Advance Next Generation Cellular Therapies

the potential of their Flow Electroporation® technology and ExPERT™ platform in the field of gene-edited cell therapeutics. By allowing Vittoria to utilize their innovative technology, MaxCyte is enabling the development and production of cutting-edge gene-edited cell therapies for T-cell lymphoma. Vittoria's lead program, Viper 101, is a promising gene-edited cell therapy specifically designed ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Centessa Pharmaceuticals Announces Dosing of First Subject in Registrational PRESent-2 Study for SerpinPC in Hemophilia B Treatment

16">The study aims to determine the effectiveness of SerpinPC in reducing bleeds in individuals with hemophilia B. Hemophilia B is a rare genetic disorder that affects the blood's ability to clot properly, leading to prolonged bleeding and increased risk of complications. Current treatment options for hemophilia B include regular infusions of clotting factors, but these can be costly and time-co..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

AIM ImmunoTech Enrolls and Doses First Subject in Phase 2 Study Evaluating Ampli

AIM ImmunoTech Inc. (NYSE American: AIM) has commenced its Phase 2 study to evaluate the potential therapeutic effects of Ampligen® on individuals with post-COVID conditions. The enrollment and dosing of the first subject have already taken place, with encouraging preliminary data on Ampligen. The study is projected to be fully enrolled by Q4 2023. In order to facilitate this study, AIM has esta..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Melinta Therapeutics Partners with BARDA to Advance Two FDA-Approved Antibiotics for Use in Pediatric Patients, and for Use Against Biothreat Pathogens

Melinta Therapeutics, LLC (Melinta), a company specializing in innovative therapies for acute and life-threatening illnesses, has joined forces with the Biomedical Advanced Research and Development Authority (BARDA) to advance two FDA-approved antibiotics, BAXDELA® and VABOMERE®, for pediatric use. Additionally, the partnership includes the development of BAXDELA® against biothreat pathogens. BA..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Infinity Pharmaceuticals Provides Additional Information on MARIO-8 Study Evaluating Eganelisib in Combination with Pembrolizumab (KEYTRUDA®)

to patients with squamous cell cancer of the head and neck. He also expressed confidence in the potential of eganelisib in combination with pembrolizumab to improve outcomes for these patients. The MARIO-8 study is part of Infinity's broader development program for eganelisib, which includes ongoing studies in other indications such as triple-negative breast cancer and non-small cell lung cancer..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Tango Therapeutics Announces First Patient Dosed in TNG462 Phase 1/2 Trial in Patients With MTAP-deleted Solid Tumors

Tango Therapeutics, a clinical-stage biotechnology company, has recently announced an important milestone in their research. The first patient has been dosed in the phase 1/2 trial of TNG462, a potential treatment for patients with MTAP-deleted solid tumors. This trial aims to assess the safety, pharmacokinetics, pharmacodynamics, and efficacy of TNG462. Notably, the drug has received Fast Track..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Completion of Enrolment and Treatment in the Phase 1 Study of MTX110 in the Treatment of Children with Newly Diagnosed Diffuse Midline Gliomas (DMGs)

Biodexa Ltd, a clinical stage biopharmaceutical company, has successfully completed the enrollment and treatment phase of the Phase 1 study for MTX110. This study focused on treating children with newly diagnosed Diffuse Midline Gliomas (DMGs), a type of primary brain tumor that primarily affects children and has a poor prognosis. The study took place at Columbia University Irving Medical Centre..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
  • textsms

Genelux Corporation Announces Publication of Phase I Trial Results of Intrapleural Administration of Olvi-Vec in Patients with Malignant Pleural Effusion from Mesothelioma, Lung or Breast Cancers in Frontiers in Immunology

Genelux Corporation, a late clinical-stage immuno-oncology company, has recently published positive Phase I trial results for their drug Olvi-Vec in the journal Frontiers in Immunology. The purpose of the trial was to assess the safety, feasibility, and immune activating effects of administering Olvi-Vec directly into the pleural cavity of patients with malignant pleural effusion (MPE) caused by..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 11.
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