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Combined safety data from RCT and OLE are presented.
Combined safety data from the RCT and OLE are presented.
Combined safety data from RCT and OLE are presented from initiation of CZP treatment to 12 wks post last visit in patients receiving ≥1 dose of CZP (Safety population, N=958).
It was of particular interest to assess the combined safety data from individual studies to help identify any significant findings, including dose response, from the pooled analysis.
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Table 6 shows the results obtained for these parameteres together with traditional odds ratio and relative risk for efficacy (i.e. without combining safety data) and for safety (i.e. without combining efficacy data).
The data are not available for each trial individually, however, but are combined with the safety data from a 3-month phase III clinical trial (for which we were unable to identify a published report) and two very short (four doses and 2 weeks, respectively) dose-ranging phase II studies.
Informed for Life releases SCORE (Statistical Combination of Risk Elements) data each year, which combine all the available safety data from the federal government and the IIHS, along with the role of weight and the presence of stability control, into a single number for each particular model, making it easier to compare vehicles of varying sizes or body types.
Outcomes are rarely of equal importance, particularly when efficacy and safety data are combined.
Safety data for testosterone and combined estrogen-androgen therapy in postmenopausal women are lacking.
Regardless, these combined antiviral and anti-amyloid activities and the encouraging safety data make CLR01 a promising broad-spectrum, topical microbicide against HIV-1 and other sexually transmitted viruses.
Safety data for the dose-titration period were analyzed using combined data from all subjects in the safety population (defined as those subjects who entered the dose-titration period and received open-label treatment).
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CEO of Professional Science Editing for Scientists @ prosciediting.com