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Bms-986278 clinical trial

WebApr 10, 2024 · A Study to Evaluate the Drug Levels, Safety, and Tolerability of BMS-986278 in Healthy Chinese Participants. The safety and scientific validity of this study is the … WebClinical Trials For: BMS-986158 ± Fedratinib, BET Inhibitor ± JAK2 Inhibitor in DIPSS–Intermediate or High-risk Myelofibrosis A Study to Assess the Safety and …

LPA1 antagonist BMS-986278 for idiopathic pulmonary …

WebMar 28, 2024 · March 28, 2024 updated by: Bristol-Myers Squibb A Double-blind, Placebo-controlled, Randomized, Single and Multiple Dose Study to Evaluate the … WebApr 10, 2024 · Bristol-Myers Squibb: ClinicalTrials.gov Identifier: NCT05805904 Other Study ID Numbers: IM027-067 : First Posted: April 10, 2024 Key Record Dates: Last Update Posted: April 10, 2024 Last Verified: March 2024 dr christopher rhody wintersville oh https://lezakportraits.com

BMS-986278 LPL Receptor Antagonist MedChemExpress

WebBMS-986278 is an experimental medication being developed and tested by Bristol-Myers Squibb. This medication blocks the ability of cells to sense a molecule called … WebJul 13, 2024 · The Autotaxin (ATX)-Lysophosphatidic Acid (LPA) Axis. Phospholipid growth factors (PLGFs) are a family of lipids with growth factor-like properties. Lysophosphatidic acid (LPA) is a member of the PLGF family that promotes a diverse range of physiological cellular functions by binding to specific G-protein-coupled receptors (LPAR 1–6), present ... WebThe purpose of this study is to provide an initial evaluation of the effectiveness of BMS-986278 in participants with lung fibrosis, to demonstrate the safety of BMS-986278, and … end xlup row空白

BMS 986278 Clinical Trials 2024 Clincosm

Category:12/20 60% 300+ - Bristol Myers Squibb

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Bms-986278 clinical trial

Inhibitors of the Autotaxin-Lysophosphatidic Acid Axis and …

WebIntroduction: The LPA1 receptor is implicated in IPF pathogenesis. BMS-986278 is a potent small molecule LPA1 receptor antagonist being investigated for IPF. This study evaluated the safety, tolerability, and PK of oral BMS-986278 in healthy participants (ppts). Methods: IM027-009 is a phase 1, double-blind, placebo (PBO)-controlled, randomized study in … WebOct 19, 2024 · An Investigational Study of Experimental Medication BMS-986278 Given With the Antibiotic Rifampin in Healthy Participants The safety and scientific validity of …

Bms-986278 clinical trial

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WebBristol Myers Squibb is committed to sustaining its strong leadership and legacy in the development of transformational therapeutics for treating patients with malignant and benign hematological conditions. • Our focus is on Multiple Myeloma, Lymphoma and CLL, MDS, AML, MPNs (e.g., myelofibrosis) and thalassemias WebJan 13, 2024 · A Phase 1, 2-Part, Randomized, Double-Blind, Placebo-controlled, Multiple Dose Study to Test the Potential Interaction of a PDE5 Inhibitor With BMS-986278 and to …

WebThe purpose of this study is to provide an initial evaluation of the effectiveness of BMS-986278 in participants with lung fibrosis, to demonstrate the safety of BMS-986278, and … WebBMS-986278, a second-generation LPA 1 antagonist, is currently in phase 2 development as a therapy for IPF and PF-ILD. Methods and analysis: This phase 2, randomised, … National Center for Biotechnology Information

WebPrincipal Scientist. Jun 2024 - Present2 years 11 months. New Jersey, United States. Allosteric inhibitor for fibrosis. • Performed SAR to improve the overall in-vitro and in-vivo profiling of ...

WebMar 28, 2024 · A Study to Evaluate the Drug Levels, Safety, and Tolerability of BMS-986278 in Healthy Chinese Participants March 28, 2024 updated by: Bristol-Myers Squibb A Double-blind, Placebo-controlled, Randomized, Single and Multiple Dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of BMS-986278 in Healthy Chinese …

WebMar 1, 2024 · Abstract. In a Phase 2 clinical trial, BMS-986020, a lysophosphatidic acid receptor-1 (LPA 6.2 μM) and inhibited BA canalicular efflux in human hepatocytes (68% … dr christopher riccioWebA Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis - IM027-040. Updated: 3 December, 2024 ... Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team dr christopher richardsWebMar 1, 2024 · BMS-986020, BMS-986234 and BMS-986278, are three lysophosphatidic acid receptor 1 (LPA1) antagonists that were or are being investigated for treatment of … dr. christopher richards-bentleyWebA Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis Latest version (submitted March 17, 2024) on ClinicalTrials.gov A … endy arfian filmWebMar 1, 2024 · BMS-986234 and BMS-986278 are both potent LPA 1 antagonists that are structurally distinct from BMS-986020 (Cheng et al., 2024) (Fig. 1).BMS-986234 was discontinued prior to clinical development due to an unfavorable nonclinical pharmacokinetic profile (Cheng et al., 2024).BMS-986278 is currently being evaluated in … endya scott san bernardino caWebFeb 3, 2024 · Clinical trial for Study to Investigate the Safety, Tolerability, and Pharmacokinetic Profile With Oral AB521 in Healthy Volunteers. Updated 02/03/2024. Toggle navigation. ... NCT03712540 - An Investigational Study of Experimental Medication BMS-986278 Given With the Antibiotic Rifampin in Healthy Participants Phase 1: … endya association courtageWebMar 1, 2024 · In a Phase 2 clinical trial, BMS-986020, a lysophosphatidic acid receptor-1 (LPA 1 ) antagonist, produced hepatobiliary toxicity (increased ALT, AST, and ALP; cholecystitis) and increases in plasma bile acids (BA). ... (BMS-986234 and BMS-986278). BMS-986020 inhibited hepatic BA efflux transporters BSEP (IC 50 1.8 μM), MRP3 (IC 50 … endy carter memphis tn