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Study Shows DecisionDx-Melanoma Provides Prognostic Information on Survival Outcomes

Study Data from Castle Biosciences’ Collaboration with the National Cancer Institute’s SEER Program Registries Published in JCO Precision Oncology &nbsp Data shows testing with DecisionDx®-Melanoma provided significant prognostic information regarding survival outcomes &nbsp FRIENDSWOOD, Texas--(BUSINESS WIRE)-- Castle Biosciences, Inc. (Nasdaq: CSTL), a company improving health through innovati..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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New Dosing Schedule for Ropeginterferon Alfa-2b Shows Improved Efficacy in Polycythemia Vera

New ropeginterferon alfa-2b Data Suggest Alternate Dosing Schedule May Achieve Greater and Quicker Complete Hematologic and Molecular Responses in Polycythemia Vera PharmaEssentia Corporation (TPEx:6446), a leading fully integrated biopharmaceutical company in Taiwan, announced today the publication of new results from a Phase 2 clinical study with ropeginterferon alfa-2b, marketed as BESREMi®, ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Delta-Fly Pharma Inc. Provides Schedule for Interim Analysis of Phase 3 Study of DFP-10917 in R/R AML

Delta-Fly Pharma Inc. has announced the schedule for the interim analysis of the Phase 3 study of DFP-10917 in relapsed/refractory acute myeloid leukemia (R/R AML) patients. The interim analysis will be based on outcome measurements including complete remission rate, overall survival, and safety. The first data processing is scheduled to be completed in mid-July 2023, followed by the second data..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Madrigal Pharmaceuticals Initiates Rolling Submission of New Drug Application for Resmetirom to FDA for NASH Treatment

Madrigal Pharmaceuticals, Inc. has announced the rolling submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for accelerated approval of its drug resmetirom for the treatment of nonalcoholic steatohepatitis (NASH) with liver fibrosis. The company expects to complete the full submission of the NDA in July 2023. &nbsp Resmetirom was granted Breakthrough Therap..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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AEON Biopharma and Priveterra Announce Arrangement of Up to $125 Million of Financing in Connection with Proposed Business Combination

AEON Biopharma and Priveterra have announced the arrangement of up to $125 million in financing for their proposed business combination. The funding includes $50 million from existing and new AEON investors, as well as cash from Priveterra's trust account. This funding will allow AEON to continue its development of a botulinum toxin complex for the treatment of medical conditions, including migr..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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SciSparc Receives Approval for Phase IIb Clinical Trial of SCI-110 to Treat Tourette Syndrome in Germany

SciSparc Receives Approval to Conduct Phase IIb Clinical Trial for SCI-110 to Treat Tourette Syndrome in Germany &nbsp TEL AVIV, Israel, June 30, 2023 (GLOBE NEWSWIRE) -- SciSparc Ltd. (Nasdaq: SPRC) ("Company" or "SciSparc"), a specialty clinical-stage pharmaceutical company focusing on the development of therapies to treat disorders of the central nervous system, today announced it has been gr..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 2.
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Aurora Spine Announces Initial Patient Enrolled for DEXA-CTM Multicenter Study

Aurora Spine Corporation, a designer and manufacturer of innovative medical devices for spinal surgery, has announced the enrollment of the first patient in its multicenter study of the DEXA-CTM Cervical Interbody System. The study aims to collect important data about the device's impact on patient outcomes. The DEXA-C system is indicated for anterior cervical interbody fusion procedures and is ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 6. 29.
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Cognition Therapeutics Announces Positive Topline Results for CT1812 Phase 2 SEQUEL Study for Mild-to-Moderate Alzheimer’s Disease

Cognition Therapeutics Inc. has announced positive topline results from its Phase 2 SEQUEL study of CT1812 in patients with mild-to-moderate Alzheimer's disease. The study showed a positive treatment effect of CT1812 on global and regional brain activity, as measured by quantitative electroencephalogram (qEEG). The results indicated a reduction in relative theta power and increased connectivity ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 6. 29.
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Foghorn Therapeutics Announces Clinical Data from Phase 1 Study of FHD-286 in Metastatic Uveal Melanoma

Foghorn Therapeutics Announces Clinical Data from Phase 1 Study of FHD-286 in Metastatic Uveal Melanoma &nbsp CAMBRIDGE, Mass., June 28, 2023 (GLOBE NEWSWIRE) -- Foghorn Therapeutics Inc. (Nasdaq: FHTX), a clinical-stage biotechnology company pioneering a new class of medicines that treat serious disease by correcting abnormal gene expression, today announced data from the Phase 1 dose escalatio..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 6. 29.
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First Wave BioPharma Announces Final Patient Dosed in Phase 2 SPAN Clinical Trial of Enhanced Adrulipase Formulation

First Wave BioPharma, a clinical-stage biopharmaceutical company specializing in gastrointestinal (GI) diseases, has announced that the final patient has been dosed in the Phase 2 SPAN clinical trial. The trial is investigating an enhanced enteric microgranule delivery formulation of adrulipase for the treatment of exocrine pancreatic insufficiency (EPI) in cystic fibrosis (CF) patients. Topline..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 6. 29.
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