The primary endpoint of the study was PFS.
研究最初的治疗终点是PFS。
The primary endpoint was overall survival (OS).
主要终点是总生存率(OS)。
The primary endpoint was 3-year larynx preservation rate.
主要评价指标是3年保喉率。
Incident lung cancer was the primary endpoint of the study.
偶发的肺癌是该研究的主要终点。
The primary endpoint will be the onset of any cardiovascular event.
主要终点是发生任何心血管事件。
The primary endpoint was clearing of ocular inflammation by day 15.
主要终点是清除眼部炎症15天。
Similar to the HL trial, the trial's primary endpoint was objective response rate.
与霍奇金氏淋巴瘤试验相似，试验主要终点是客观缓解率。
The primary endpoint of the trial was to reduce the risk of tumour progression.
试验的初级预期目标是降低肿瘤进展的危险程度。
The primary endpoint was overall survival, and analysis was done by intention to treat.
主要终点指标为总生存期，资料分析采用意向处理分析。
BENLYSTA has successfully met its primary endpoint in two pivotal Phase 3 trials in systemic lupus.
BENLYSTA已经成功地达到其主要终点的两个关键第三阶段试验的系统性。
RESULTS: There was significant improvement in the primary endpoint in the 25-mg and 50-mg groups vs placebo.
结果：在用25毫克和50毫克患者对比安慰剂组中，试验主要终末点之间并无显著改善。
The primary endpoint was assessed for 375 women allocated to receive vitamins, and 374 allocated to placebo.
评价了补充维生素的375例女性以及安慰剂的374例女性的主要终点。
The primary endpoint was overall survival, and secondary endpoints included PFS and objective response rate (ORR).
主要指标是总生存期，次要指标包括无进展生存期(PFS)和客观反应率(ORR)。
So we are actually optimistic despite being disappointed that the overall trial did not achieve its primary endpoint.
因此我们实际上是非常乐观的，尽管对试验未能达到主要终点而感到失望。
In general, all randomized patients were included in the final intent-to-treat analysis for survival (primary endpoint).
总的来说，所有随机分组的患者包括在最终的意愿性治疗生存分析（主要终点）中。
Can you give us a brief introduction of this trial and what do you think about the negative results for the primary endpoint?
您能简要为我们介绍一下该试验吗？您怎么看待主要终点的阴性结果？
Clinical cure, the primary endpoint, was defined as a reduction of at least 75% on the Acute Bronchitis Severity Score at 14 days.
研究的基本终止点即临床治愈的评判标准为14天后至少75%的患者的急性气管严重度评分降低。
A conditional power calculation showed a low probability that the primary endpoint (25% EFS improve by allo SCT) could still be met.
假定的能耗计算显示，虽然概率较低，但是可以达到主要终点(异体移植的EFS改善25%)。
The primary endpoint was PFS, which was defined as the interval between initial treatment and the first documentation of disease progression or death.
研究的首要观察终点为PFS，其定义为初始治疗至第一次记录疾病进展或死亡的间期。
The primary endpoint in this arm is survival without stroke or death and superiority to medical therapy. This trial arm has enrolled 14 patients to date.
一级终点为无中风的生存，死亡和优于药物治疗，目前已入选了14例患者。
The primary endpoint was change from baseline in the total score of the Unified Parkinson's Disease Rating Scale (UPDRS) Part III at the final assessment point.
最后评估总根据统一帕金森疾病评定量表（UPDRS）第三部分的总评分中试验主要终末点相对于试验初期有所改变。
The study’s primary endpoint was objective response rate, the percentage of patients who experienced complete or partial cancer shrinkage or disappearance after treatment.
研究主要终点是客观缓解率，治疗后经受完全或部分癌症皱缩或消失患者的百分率。
The primary endpoint was the highest value of adenosine diphosphate –induced PA measured with LTA in the weeks after complete cessation of clopidogrel in both groups.
主要终点是两组在完全停药后数周内用光透集合度测定法测量的二磷酸腺苷诱导的血小板聚集的最高值。
Multaq met its primary endpoint in the trial, reducing the risk of death or hospitalization due to cardiovascular events in patients with atrial fibrillation, when compared to placebo.
Multaq在该试验中达到预期疗效，与安慰剂相比，该药可降低房颤（AF）患者由心血管疾病所致的死亡或住院治疗风险。
But based on the protocol-specified initial analysis, exercise training produced only a modest, non-significant reduction in the primary endpoint of all-cause hospitalization or all-cause death.
但根据协议规定的初步分析，运动训练只产生少量的非显着减少主要终点各种原因住院或各种原因死亡。
Hemoglobin A1c levels started out similar between treatment arms and averaged a similar 7.2% to 7.4% at 16 weeks with no significant differences for the primary endpoint of change in hemoglobin A1c.
糖化血红蛋白水平之间开始了类似的武器和治疗16周，平均每场类似的7.2%至7.4%的为在糖化血红蛋白变化的主要终点无显着差异。
In both studies, the primary efficacy endpoint was progression-free survival.
在两项研究中，主要功效评估指标是无进展生存期。
In both studies, the primary efficacy endpoint was progression-free survival.
在两项研究中，主要功效评估指标是无进展生存期。
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