WitrynaData from the IMerge Phase 2 were recently presented at the American Society of Hematology Annual Meeting and support the ongoing Phase 3. “Reaching fty percent enrollment is a key milestone towards the completion of this registration-enabling Phase 3 clinical trial, and we appreciate all of the support from our investigators and the … Witryna15 lis 2024 · Methods: IMerge (MDS3001; NCT02598661) is a global, phase 2/3 study of imetelstat in RBC TD, ESA-R/R LR-MDS. After an initial analysis, the phase 2 study …
iMerge - CSI Docs
Witryna4 sty 2024 · About IMerge Phase 3. The Phase 3 portion of the IMerge Phase 2/3 study is a double-blind, 2:1 randomized, placebo-controlled clinical trial to evaluate imetelstat in patients with IPSS Low or Intermediate-1 risk (lower risk) transfusion dependent MDS who were relapsed after, refractory to, or ineligible for, erythropoiesis stimulating agent ... Witryna16 sie 2024 · Geron Corporation, a late-stage clinical biopharmaceutical company, today reported updates on the IMerge Phase 3 trial in lower risk MDS and financial results for the second quarter ended June 30 ... flush signals with running lights
Geron to Present at Upcoming Investor Conferences in April
WitrynaThe Phase 2 part of IMerge demonstrated an 8-week RBC transfusion independence (RBC-TI) rate of 42%, 24-week RBC-TI rate of 32%, with median duration of TI being 88 weeks. The responses were seen across different subtypes of LR MDS (Platzbecker et al, EHA 2024, S183). No new safety signal was identified. WitrynaiMerge is designed to do what the end user cannot do. That is, merge activities, financial transactions, orders, event registrations, and certification from one record to another. It can optionally delete the name information from the old or "bad" record. In addition, iMerge is designed to protect you from corrupting the two merged records. flush side mount nav lights