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During the second 6 months of the trial, the responses associated with abatacept were maintained, while those observed with infliximab were not.
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In this trial, the response rate to EDP-M was 23.2 % and the median progression-free survival interval was 5 months [15].
In the original trial, the response rate was 30%, time to progression 4 months, and median survival 9 months[5].
The first step was similar to the texture information measure except that trials were pooled based on the side of the reward, so that on every trial the response was labeled left or right, with texture identity dropped.
In this trial the response to nutrient supplementation in pregnancy varied by outcome.
In this trial the response rate was 20% as assessed by the investigator and 14% by an external Response Evaluation Committee.
In this trial the response rate was impressive with an overall response of 69% (24% CR), and was well tolerated.
In the present trial the response to the different doses did not depend significantly on whether a child had received VAS at birth (Table 3).
If an infant did not move his/her eyes from the central face during the trial, the response was coded as a fixation response on the face.
In patients with metastatic melanoma treated in the phase I portion of the trial, the response rate was 26% (9 of 35 patients) [68].
In the preliminary report of this trial, the response rate was 30%, and the median progression-free survival and overall survival were 4.4 months and 12.5 months, respectively.
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CEO of Professional Science Editing for Scientists @ prosciediting.com