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Parinux therapy. A total of 2213 patients were randomized and 2184 were treated. Patients ranged in age from 18-97 years mean age 62 years ; with 44% men and 56% women. Patients were 94% Caucasian, 5% Black and 1% other races. Patients with serum creatinine level more than 2 mg dL 180 mol L ; , or platlet count less than 100, 000 mm3 were excluded from the trial. For both groups, treatment continued for at least 5 days with a treatment duration range 7 2 days, and both treatment groups received Vitamin K antagonist therapy initiated within 72 hours after the first study drug administration and continued for 90 7 days, with regular dose adjustments to achieve an INR of 2-3. The primary efficacy endpoint was confirmed, symptomatic, recurrent VTE reported up to Day 97. The efficacy data are provided in Table 6 below and psilocybin.

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