Ion-682884-cs3
Web23 sep. 2024 · Inclusion Criteria: Satisfactory completion of ION-682884-CS3 (NCT04136184) (Index Study) as judged by the Investigator and Sponsor, or diagnosis of hATTR-PN and satisfactory completion of either study ISIS 420915-CS101 or study 2024-P001436 (NCT03702829) (both are Investigator-Sponsored studies with inotersen - the … WebThe EU Clinical Trials Register currently displays 43188 clinical trials with a EudraCT protocol, of which 7144 are clinical trials conducted with subjects less than 18 years old. The register also displays information on 18700 older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).
Ion-682884-cs3
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Web13 nov. 2024 · ION-682884-CS2 (EudraCT No: 2024-002835-27) is a Phase 3 global, double-blind, randomized, placebo-controlled study assessing the efficacy and safety of … Web28 feb. 2024 · 5. Coelho T, Ando Y, Benson MD, Berk JL, Waddington-Cruz M, Dyck PJ, et al. Design and rationale of the global phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-L Rx (ION-682884-CS3) in hereditary transthyretin-mediated amyloid polyneuropathy. Neurol Ther. (2024) 10:375–89. doi: 10.1007/s40120-021-00235-6
Web23 okt. 2024 · Coelho T, Ando Y, Benson MD, Berk JL, Waddington-Cruz M, Dyck PJ, Gillmore JD, Khella SL, Litchy WJ, Obici L, Monteiro C, Tai LJ, Viney NJ, Buchele G, Brambatti M, Jung SW, St L O'Dea L, Tsimikas S, Schneider E, Geary RS, Monia BP, Gertz M. Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense … Web2 nov. 2024 · Participants received ION-682884 matching placebo, subcutaneously (SC) once every 4 weeks [Q4W] (total of 4 doses) along with daily oral supplemental doses of …
WebCS3 – Phase 3 study in patient with PN Research type Research Study Full title A Phase 3 Global, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of ION … WebInclusion Criteria: Satisfactory completion of ION-682884-CS3 (NCT04136184) (Index Study) as judged by the Investigator and Sponsor, or diagnosis of hATTR-PN and satisfactory completion of either study ISIS 420915-CS101 or study 2024-P001436 (NCT03702829) (both are Investigator-Sponsored studies with inotersen – the …
Web26 feb. 2024 · AKCEA-TTR-L Rx (ION-682884) is a ligand-conjugated antisense (LICA) drug designed for preferential delivery to hepatocytes, the primary source of systemically …
Web8 okt. 2024 · A Study to Assess the Long-Term Safety and Efficacy of Eplontersen (Formerly Known as ION-682884, IONIS-TTR-LRx and AKCEA-TTR-LRx) in Patients With … how to run python on ubuntuWeb27 mrt. 2024 · Eplontersen demonstrated sustained benefit in Phase III trial for hereditary transthyretin-mediated amyloid polyneuropathy (ATTRv-PN) through 66 weeks. … how to run python in ubuntuWeb21 jun. 2024 · Coelho T, et al. Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-LRx(ION-682884-CS3) in Hereditary Transthyretin-Mediated Amyloid Polyneuropathy. Neurol Ther. 2024 Jun;10(1):375-389. how to run python on a macWeb8 okt. 2024 · 1 Effectiveness 2 Safety Daratumumab for Amyloidosis 18+ All Sexes Duarte, CA This trial is testing a new cancer treatment to see if it is safe for people with heart problems. The new treatment is a combination of drugs, and the trial will also look at how well it works in people of different racial and ethnic backgrounds. Phase 2 Recruiting how to run python program in jupyterWebA Study to Assess the Long-Term Safety and Efficacy of ION-682884 in Patients With Hereditary Transthyretin-Mediated Amyloid Polyneuropathy. This is a multicenter, open … how to run python on mac terminalWeb13 apr. 2024 · An Open-Label Study of ION-682884 in Patients With TTR Amyloidosis Who Have Completed a 24-Open Label Study of Inotersen for TTR Amyloidosis … how to run python .py fileWeb10 mrt. 2024 · A Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single-Ascending and Multiple Doses of Eplontersen (Formerly … how to run python on vscode