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Last updated at November 11th, 2020Microsoft Internet Information Services 8 - ASLeap
Status : OnlineAbout the Study. During this one-year study, the information participants provide will help doctors better understand how the investigational drug affects patients who have been diagnosed with AS. During the study, participants will receive: Individual care and assessments from a specialized health care provider
Status : Onlineflorida Participating Areas. Aventura, Boca Raton, Brandon, Deland, Gainesville, Hialeah, Ocoee, Orlando, Plantation, St. Petersburgh, Tamarac, Tampa, Vero Beach ...
Status : OnlineUser Login. A new computerized medical test for assessment of Health Risk . Based on HRV method. User Login.
Status : OnlineAsleap will examine traffic to identify the LEAP or PPTP challenge/response process and will extract the username, challenge and response information. This can be done in a passive operation with a 802.11 card in RFMON mode, or through an active attack, where asleap impersonates the legitimate access point, and forces the victim to ...
Status : OnlineThe study is expected to begin enrollment in January 2018 and aims to enroll approximately 270 patients at 70 centers in the United States. The ASLeap study design includes an initial 16 week open-label period (Treatment Period 1), followed by a randomized, double-blind, parallel-group period (Treatment Period 2).
Status : Online(ASLeap) Study Estimating the Clinical Difference Between 300 mg and 150 mg of Secukinumab Following Dose Escalation to 300 mg in Patients With Ankylosing Spondylitis Purpose The purpose of this study is to discover if it is beneficial to double the standard dose of the biologic drug Cosentyx for patients with Ankylosing Spondylitis (AS).
Status : OnlineThe study is expected to begin enrollment in January 2018 and aims to enroll approximately 270 patients at 70 centers in the United States. More information can be found at www.clinicaltrials.gov. The ASLeap study design includes an initial 16 week open-label period (Treatment Period 1), followed by a randomized, double-blind, parallel-group ...
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