Web15 jun. 2024 · A phase 2a study by Ionis Pharmaceuticals using TMPRSS6 inhibitors will soon be initiated in patients with NTDT ≥ 18 years of age. In this study patients will be subcutaneously administered IONIS TMPRSS6-LRx every 4 weeks (ClinicalTrials.gov number NCT04059406) (Table 2). Web31 dec. 2024 · Dynacure advanced IONIS-DNM2-2.5Rx, resulting in $7.5 million in payments from Dynacure Advancing additional programs in Ionis' clinical pipeline for diseases with unmet medical need Initiated a Phase 2 study of sapablursen (formerly known as IONIS-TMPRSS6-LRx) in patients with polycythemia vera, the second indication for …
Clinical trial Mechanism of Condition (Phase) Company NCT
Web3 dec. 2024 · A Study to Evaluate IONIS-TMPRSS6-LRx (ISIS 702843) in Patients With Polycythemia Vera Condition: Phlebotomy Dependent Polycythemia Vera Intervention: Drug: IONIS-TMPRSS6-LRx Sponsor: Ionis Pharmaceuticals, Inc. Web25 aug. 2024 · This is a Phase 2a, multi-center, randomized, open-label study of IONIS-TMPRSS6-LRx in up to 40 participants with PD-PV. The study consists of 3 periods: 1) … dachshund rescue maryland virginia
A Study to Evaluate IONIS-TMPRSS6-LRx (ISIS 702843) in …
Web27 mrt. 2024 · Blood samples for IONIS-TMPRSS6-Lrx PK will also be collected at the Early Termination visit for all cohorts (if it occurs). Urine for IONIS-TMPRSS6-Lrx PK will be collected at the following intervals: Cohorts A, B, and C: time of dosing on Day 1 to 24 hours post-dose on Day 2; time of dosing on Day 57 to 24 hours post-dose on Day 58. Web14 aug. 2024 · Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Sapablursen (Formerly ISIS 702843, IONIS-TMPRSS6-LRx) … WebA Study to Evaluate Sapablursen (Formerly ISIS 702843, IONIS-TMPRSS6-LRx) in Patients With Polycythemia Vera Study Purpose The main purpose of this study is to evaluate the … binks dim witted character from star wars