Reach2 protocol
WebJun 29, 2024 · REACH2 required alpha-fetoprotein greater than 400 ng/mL for eligibility and, as we know, determined a statistically significant survival benefit and secondary end point … WebREACH2 study involving 309 patients with gluco - corticoid-refractory acute GVHD showed that ... trial to the protocol (available at NEJM.org). The trial was designed and conducted in accordance
Reach2 protocol
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WebApr 22, 2024 · The results of REACH2, the first Phase III study in acute GvHD to have met its primary endpoint, reinforce findings of the previously reported Phase II REACH1 study. … WebDec 23, 2024 · Usama Gergis, MD, MBA: This was rightfully followed by the REACH2 trial, which was a phase 3 randomized trial for steroid-refractory acute GVHD patients. I’ll get into definition and differences from the REACH-1 trial. Patients were randomized to either ruxolitinib 10 mg twice a day or investigator choice.
WebJun 1, 2024 · 4003 Background: Patients (pts) with advanced HCC and elevated AFP have a poorer prognosis compared to the general HCC population, and need effective, well … WebApr 27, 2024 · Data from the phase III REACH2 study, published in The New England Journal of Medicine, demonstrated that ruxolitinib (Jakafi) therapy led to significant improvements in efficacy outcomes in patients with steroid-refractory acute graft-versus-host disease (GVHD) compared to the best available therapy. 1
WebApr 22, 2024 · In REACH2, patients treated with ruxolitinib experienced a significantly greater overall response rate (ORR) vs. BAT (62% vs. 39%; p<0.001) at Day 28, the primary endpoint of the study. For the key secondary endpoints, patients treated with ruxolitinib maintained significantly higher durable ORR (40% vs. 22%; p<0.001) at Day 56. WebJul 21, 2024 · REACH2 was a great validation of the REACH1 results. REACH2 was a phase 3 international trial, and it involved 309 patients with steroid-refractory aGVHD. Patients …
WebApr 22, 2024 · REACH2 was a multicenter, randomized, open-label, phase 3 trial. Patients (or their guardians) provided written informed consent, and patients were then assessed …
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