Tīmeklis2024. gada 5. apr. · 1 LAM-002A is the formulation of AIT-101 used in the current Phase 2 study 2 Clinicaltrials.gov identifier: NCT05163886. CONTACT: MEDIA CONTACT: [email protected]. TRENDING. 1. Tīmeklis2016. gada 26. febr. · LAM-002A is an oral selective kinase inhibitor currently undergoing Phase I trials for the treatment of relapsed or refractory B-cell non-Hodgkin lymphoma. These trials seek to evaluate the safety, tolerability, and pharmacokinetics of LAM-002A. Before investigation of LAM-002A in patients with lymphoma, it was …
Results of a completed phase I study of LAM-002 (apilimod …
Tīmeklis2024. gada 12. aug. · The LAM-002A dose may be reduced to 100 mg BID (200 mg total daily dose) if expected gastrointestinal side effects develop. Participants who complete the first 12 weeks of the Core Study will be eligible to receive active drug (LAM-002A capsules at maximum tolerated dose of 125 or 100 mg BID) for the … Tīmeklis*LAM-002A is the current formulation being studied in the AIT-101 program To learn more, click here to visit ClinicalTrials.gov. (ClinicalTrials.gov Identifier: … how to say in english in japanese
Study of Safety, Tolerability, and Biological Activity of LAM-002A …
Tīmeklis2024. gada 7. dec. · LAM-002A is a highly potent and selective inhibitor of PIKfyve that disrupts lysosomal homeostasis resulting in cytotoxic activity in multiple B-cell … Tīmeklis2024. gada 8. marts · Other Clinical Trials. PA15-0575 Observational prospective Research study In monoclonal Gammopathies leadINg to myeloma (ORIGIN study) 2024-1088 A Multicenter, Open-label Feasibility Study of Daratumumab with Dose-Adjusted EPOCH in Newly Diagnosed Plasmablastic Lymphoma with or without HIV. Tīmeklis2024. gada 24. jūn. · A Study of LAM-002A for the Prevention of Progression of COVID-19. The safety and scientific validity of this study is the responsibility of the study … north italian vs south italian