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SPID separated between sufentanil and placebo treated patients after the first hour, and was highly significant at all timepoints thereafter as illustrated below.

study. The oldest patient treated was 90 years of age, the heaviest had a BMI of 62 kg/m2. Historically, older patients are more susceptible to the adverse events caused by opioids, and heavier patients tend to have greater risk of obstructive apnea, which is often worsened by opioids. This should allow Belts Ferragamo

Male: FemaleBMI (kg/m2) 30

As with our other Phase 3 studies, there was no upper limit on age or weight in recruitment of patients in this Hermes Belts For Sale

Top line Data Demonstrate Primary Endpoint Achieved in Final Pivotal Phase 3 of NanoTab PCA System For Management of Post Operative Pain

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the regulatory agency to review data for treating these two at risk groups with sufentanil. Overall, patient demographics (percentage of patients) in this study were as follows:

Age (yrs)Primary Endpoint Data

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REDWOOD CITY, Calif., May 21, 2013 /PRNewswire/ AcelRx Pharmaceuticals, Inc. (Nasdaq: ACRX), a specialty pharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of acute and breakthrough pain, today announced top line data demonstrating that in a placebo controlled Phase 3 study of its investigational sublingual NanoTab PCA (patient controlled analgesia) System (NanoTab System), the primary efficacy endpoint was achieved. ). Results demonstrated that patients receiving sufentanil NanoTabs realized a significantly greater during the study period than placebo treated patients (+76.1 vs , p

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AcelRx Pharmaceuticals Drug Device Meets Main Hermes Belt Womens Goal of Late Stage Study

System with a 20 minute lock out period. Patients in both groups could receive up to 2 mg morphine intravenously per hour as a rescue medication, the primary purpose of this rescue medication being to enable placebo treated patients to stay in the study. Pain scores recorded just prior to the delivery of rescue medication were gathered and imputed forward to minimize the impact of this rescue opioid on efficacy evaluations.

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Two hundred fifteen (68.3%) sufentanil NanoTab treated patients completed the 48 hour study period, compared to 43 (41.3%) placebo treated patients. Primary reasons for drop out in the sufentanil and placebo treated groups were adverse events (7.0% and 6.7%, respectively) and lack of efficacy (14.3% and 48.1%, respectively). The primary endpoint measure, , was +76.1 for sufentanil treated patients and for placebo treated patients (p

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"With the successful completion of this study, AcelRx has now achieved positive results in all three Phase 3 studies in which the NanoTab PCA System has been evaluated," said Richard King, president and CEO of AcelRx. sites for treatment of moderate=to severe acute pain immediately following major orthopedic surgery. Seven patients did not receive study drug, resulting in 419 patients being included in the intent to treat (ITT) population. Patients were treated for a minimum of 48 hours, and up to 72 hours. Patients were randomized 3:1, with 315 patients randomized to sufentanil treatment and 104 to placebo treatment. Both treatments were delivered by the patient, as needed, using the NanoTab Gucci Belt Sale Womens

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