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BioCardia Announces Pause in Enrollment for Phase III Pivotal CardiAMP Cell Therapy Heart Failure Trial

BioCardia Announces Pause in Enrollment for Phase III CardiAMP Cell Therapy Heart Failure Trial SUNNYVALE, Calif., July 24, 2023 (GLOBE NEWSWIRE) -- BioCardia, Inc. [Nasdaq: BCDA], a developer of cellular and cell-derived therapeutics for cardiovascular and pulmonary disease treatment, has received a recommendation from the independent Data Safety Monitoring Board (DSMB) to temporarily pause new..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 24.
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Teleflex Completes Enrollment in RingerTM PTCA Study

Teleflex Completes Enrollment in Percutaneous Coronary Intervention Study Teleflex Incorporated, a leading global provider of medical technologies, has announced the successful completion of patient enrollment in the RingerTM PTCA study. This groundbreaking study is one of two clinical trials that aim to evaluate the performance and effectiveness of the innovative RingerTM Perfusion Balloon Cath..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 19.
  • textsms

Grifols Meets Enrollment Target in Phase 3 Study of Two Dose Regimens of Prolastin®-C in Patients with Emphysema Due to Alpha-1-Antitrypsin Deficiency

Grifols Successfully Enrolls Targeted Number of Patients in Phase 3 Study of Prolastin®-C for Emphysema Due to Alpha-1-Antitrypsin Deficiency Grifols, a global leader in plasma-derived medicines, has achieved its enrollment goal of 339 patients for the SPARTA clinical trial. This groundbreaking study aims to assess the effectiveness and safety of two different weekly doses of Grifols' Prolastin®..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 14.
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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.
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Palisade Bio Announces Completion of Enrollment in LB1148 Dose Optimization Study

Palisade Bio, a biopharmaceutical company focused on gastrointestinal complications, has announced the completion of patient enrollment in its LB1148 dose optimization study. The study aims to generate valuable data on pharmacokinetics and pharmacodynamics across multiple doses in healthy adult volunteers. This milestone brings Palisade Bio closer to obtaining Phase 2 topline data for the preven..

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

Ayala Pharmaceuticals Announces Successful End-of-Phase 2 Meeting with FDA Regarding AL102 for the Treatment of Desmoid Tumors

Ayala Pharmaceuticals, Inc. has successfully concluded an End-of-Phase 2 meeting with the FDA regarding AL102, a potential treatment for desmoid tumors. The company confirms agreement with the FDA on key elements of the Phase 3 segment of the ongoing RINGSIDE study, including the dosing regimen. Enrollment in Phase 3 is continuing as planned. Desmoid tumors are rare connective tissue tumors that..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 7. 6.
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Seelos Therapeutics Closes Enrollment of Study for Intranasal Ketamine Treatment for Acute Suicidal Ideation and Behavior in Major Depressive Disorder Patients

Seelos Therapeutics has completed enrollment in its registration-directed study of SLS-002, an intranasal racemic ketamine for treating acute suicidal ideation and behavior (ASIB) in adults with major depressive disorder (MDD). The two-part clinical trial includes an open-label cohort followed by a randomized, double-blind, placebo-controlled study. Seelos aims to address the unmet need for ther..

  • format_list_bulleted Pharmacology/BS
  • · 2023. 6. 23.
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