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Positive Aggregate Safety Data From Vafidemstat’s Ongoing Phase IIb PORTICO Trial in Borderline Personality Disorder

Positive Aggregate Safety Data From Vafidemstat’s Ongoing Phase IIb PORTICO Trial in Borderline Personality Disorder &nbsp Recommendation from the independent Data Monitoring Committee (DMC) to continue the PORTICO trial based on positive safety data from the initial 167 randomized patients. PORTICO plans to recruit 188 patients. &nbsp MADRID, Spain and BOSTON, July 05, 2023 (GLOBE NEWSWIRE) -- ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 6.
  • textsms

InnoCare Announces First Psoriasis Patient Dosed in Clinical Trial of TYK2 Allosteric Inhibitor ICP-488 in China

InnoCare Announces First Psoriasis Patient Dosed in Clinical Trial of TYK2 Allosteric Inhibitor ICP-488 in China BEIJING--(BUSINESS WIRE)-- InnoCare Pharma (HKEX: 09969; SSE: 688428), a leading biopharmaceutical company focusing on the treatment of cancer and autoimmune diseases, announced today the first psoriasis patient has been dosed in clinical trial of the Company’s TYK2 (tyrosine kinase 2..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 5.
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Lunit's AI-Powered Lung Cancer Screening Solution Significantly Affects Radiologists' Diagnostic Determination

Lunit's AI-Powered Lung Cancer Screening Solution Significantly Affects Radiologists' Diagnostic Determination - Published in Radiology A recent study conducted by Seoul National University Hospital provides strong evidence that a high-accuracy AI model improves radiologists' chest X-ray analysis performance. Lunit, a global provider of AI-powered cancer diagnostics solutions, announced the publ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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CANbridge to Continue CAN008 Phase 2 Trial in Glioblastoma Multiforme (GBM) in China Based on Interim Analysis of Independent Data Monitoring Committee

CANbridge Pharmaceuticals, Inc. (1228.HK), a global biopharmaceutical company based in China, has announced that it will continue the Phase 2 trial of CAN008 in patients with glioblastoma multiforme (GBM) in China. This decision is based on the interim analysis recommendation of the independent data monitoring committee. The ongoing Phase 2 study aims to evaluate the efficacy and safety of CAN00..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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Journey Medical Corporation Expects Topline Results from Phase 3 Clinical Trials Evaluating DFD-29 for the Treatment of Rosacea

Journey Medical Corporation Expects Topline Results from the Phase 3 Clinical Trials (MVOR-1 and MVOR-2) Evaluating DFD-29 Journey Medical Corporation (Nasdaq: DERM), a commercial-stage pharmaceutical company, announced that it anticipates releasing topline results from two Phase 3 clinical trials evaluating DFD-29 for the treatment of moderate to severe papulopustular rosacea. The results are e..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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Abeona Therapeutics Announces $25 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules

Abeona Therapeutics Inc. (Nasdaq: ABEO) has successfully raised $25 million through a registered direct offering under Nasdaq rules. The funds were primarily raised to support the launch preparations for the Company's EB-101 Biologics License Application (BLA) submission and potential approval. Abeona entered into definitive agreements with existing institutional investors, issuing and selling 3..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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NLS Pharmaceutics to Proceed with Phase 3 Clinical Program (AMAZE) for Mazindol ER for the Treatment of Narcolepsy Following FDA Review and IRB Approval of the Full Study Protocol

NLS Pharmaceutics, a Swiss clinical-stage biopharmaceutical company, has received approval from the U.S. Food and Drug Administration (FDA) to proceed with its Phase 3 clinical program for Mazindol ER in the treatment of narcolepsy. The full study protocol, called AMAZE, was reviewed by the FDA and also received approval from the independent Institutional Review Board (IRB). This milestone allow..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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Datopotamab Deruxtecan Demonstrates Progression-Free Survival in Advanced Non-Small Cell Lung Cancer

Datopotamab Deruxtecan Met Dual Primary Endpoint of Progression-Free Survival in Patients With Advanced Non-Small Cell Lung Cancer in TROPION-Lung01 Phase III Trial &nbsp Positive high-level results from the TROPION-Lung01 Phase III trial showed that datopotamab deruxtecan (Dato-DXd) demonstrated a statistically significant improvement for the dual primary endpoint of progression-free survival (..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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Fresenius Kabi Introduces IDACIO® (adalimumab-aacf) as its First Immunology Biosimilar in the United States

Fresenius Kabi, a global healthcare company specializing in medicines and technologies, has announced the availability of its first immunology biosimilar, IDACIO® (adalimumab-aacf), in the United States. IDACIO® is indicated for use in the treatment of chronic autoimmune diseases and is a biosimilar to Humira® (adalimumab). It is available in a self-administered prefilled syringe and pre-filled ..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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Labcorp Completes Spin-off of Fortrea

Labcorp, a global leader in laboratory services, has successfully completed the spin-off of Fortrea, an independent Contract Research Organization. Fortrea will now offer clinical trial management and technology solutions to pharmaceutical and biotechnology organizations on a global scale. The company is set to begin trading on the NASDAQ Stock Market under the symbol "FTRE." Expressing his grat..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 4.
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