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Roche's Tecentriq Improves Survival in NSCLC Patients Ineligible for Platinum Chemo

Roche’s Tecentriq has been shown to improve survival in non-small cell lung cancer (NSCLC) patients who are not eligible for platinum-based doublet chemotherapy, according to data from the Phase III IPSOS trial. The study, led by University College London (UCL) and supported by Roche, revealed its findings in The Lancet. The results showed that patients treated with Tecentriq had a median overal..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 8.
  • textsms

Phil Inc. Partners with RedHill Biopharma to Increase Access to Talicia®

Celldex Therapeutics, Inc. has initiated their Phase 2 study of barzolvolimab in eosinophilic esophagitis (EoE) with the dosing of the first patient. EoE is a chronic inflammatory disease that affects the esophagus and is the most common form of eosinophilic gastrointestinal disease. The objective of this study is to assess the effectiveness and safety of subcutaneous barzolvolimab in patients w..

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

Publication of Manuscript from the PNOC015 (a.k.a. MTD-201) Study in Patients with Diffuse Midline Glioma (DMG)

Scientific Officer of Biodexa Pharmaceuticals PLC, expressed his satisfaction with the study's results. He emphasized that the study provided valuable insights into the safety and efficacy of intra-tumoral administration of MTX110 via CED. The success of this study has led to a follow-up Phase I study at Columbia University.

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

Secarna Pharmaceuticals Demonstrates Therapeutic Activity of LNAplus™ ASO Targeting NLRP3 in Autoinflammatory Diseases

Secarna Pharmaceuticals, a biopharmaceutical company specializing in antisense oligonucleotide (ASO) therapies, has published new preclinical data in The Journal of Immunology. The data demonstrates the potent therapeutic activity of their LNAplus(TM) ASO targeting NLRP3 in debilitating autoinflammatory diseases. NLRP3 is a central component of the inflammasome pathway, which is overactive in ma..

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

Shorla Oncology Announces Licensing Agreement and Strategic Partnership for Rights to Market Chemotherapy Drug, PIP-101, in the United States

Shorla Oncology Announces Licensing Agreement and Strategic Partnership for Rights to Market Chemotherapy Drug, PIP-101, in the United States &nbsp The developer is a United Kingdom-based drug development and manufacturing company, providing integrated R&D and manufacturing capabilities to accelerate entry of PIP-101 in the U.S. market. Shorla Oncology to receive the exclusive rights to commerci..

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

Incannex Receives Ethics Approval for Bioequivalence/Bioavailability Clinical Trial for IHL-42X, the Company’s Proprietary Drug for Treatment of Obstructive Sleep Apnoea (‘OSA’)

Incannex Healthcare Limited has received approval from the Bellberry Human Research Ethics Committee to conduct a bioequivalence/bioavailability clinical trial for their proprietary drug, IHL-42X. This drug is specifically designed for the treatment of obstructive sleep apnoea (OSA). The trial will involve 116 participants and will be managed by Novotech at CMAX Clinical Research in South Austra..

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

Hillstream BioPharma Licenses Technology to Develop Proprietary HER2 and HER3 Antibody Drug Conjugates against Drug-Resistant Breast, Lung, Gastric, and Ovarian Cancers

Hillstream BioPharma Licenses Technology to Develop Proprietary HER2 and HER3 Antibody Drug Conjugates against Drug-Resistant Breast, Lung, Gastric, and Ovarian Cancers &nbsp Hillstream BioPharma, Inc. (Nasdaq: HILS) ("Hillstream" or the "Company") has announced an exclusive agreement with Applied Biomedical Science Institute (ABSI) to license technology for human antibodies targeting novel HER2..

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

Simcha Therapeutics Announces First Patient Dosed in Phase 1/2 Study Evaluating ST-067 in Combination with KEYTRUDA® (Pembrolizumab) in Patients with Various Solid Tumors

Simcha Therapeutics, a clinical-stage immunobiology company, has announced that the first patient has been dosed in a Phase 1/2 clinical trial of ST-067 in combination with Merck's anti-PD-1 therapy, KEYTRUDA®, for patients with advanced solid tumors. The study aims to determine the maximum tolerated dose and preliminary activity of the combination treatment. Simcha Therapeutics has observed pro..

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

FDA Removes Partial Clinical Hold on TakeAim Leukemia Study, RP2D Established at 300 mg BID

Curis, Inc., a biotechnology company focused on the development of emavusertib, an orally available small molecule triple target inhibitor (IRAK4, FLT3 and CLK) for the treatment of hematologic malignancies, announced that the U.S. Food and Drug Administration (FDA) has removed the partial clinical hold on the TakeAim Leukemia Phase 1/2 study of emavusertib. The recommended phase 2 dose (RP2D) f..

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

Carrick Therapeutics Announces Clinical Trial Collaboration with Arvinas and Pfizer to Evaluate Samuraciclib and Vepdegestrant Combination

Carrick Therapeutics, an oncology focused biopharmaceutical company, has announced a collaboration with Arvinas Inc. and Pfizer Inc. for a clinical trial involving the combination of two drugs, samuraciclib (CT7001) and vepdegestrant (ARV-471). The trial aims to evaluate the effectiveness of this innovative combination, which involves Carrick's samuraciclib, an oral CDK7 inhibitor, and Arvinas' ..

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