The Potential Geographical Distribution of Bactrocera cucurbitae (Diptera: Tephritidae) in China Based on Eclosion Rate Model and ArcGIS

Abstract. The melon fruit fly, Bactrocera cucurbitae Coquillett (Diptera: Tephritidae), is one of the important insect pests of fruits and vegetables. In order to monitor and control it effectively, it is necessary to know the potential geographical distribution of this pest. The ER (Eclosion rate) model was constructed from empirical biological data, and analyzed with ArcGIS. Based on the soil temperature and moisture data of Chinese meteorological stations, the potential geographical distribution of B. cucurbitae from January to December in China was predicted. Six categories were used to describe different levels of suitability for B. cucurbitae in China. The potential geographical distribution and suitable levels for every month in China were obtained and showed that almost all locations were suitable from May to September. Further analysis showed that monitoring measures should be taken in Guangdong, Guangxi, Yunnan, and Hainan provinces throughout the year

Research designs for proof-of-concept chronic pain clinical trials: IMMPACT recommendations

Proof-of-concept (POC) clinical trials play an important role in developing novel treatments and determining whether existing treatments may be efficacious in broader populations of patients. The goal of most POC trials is to determine whether a treatment is likely to be efficacious for a given indication and thus whether it is worth investing the financial resources and participant exposure necessary for a confirmatory trial of that intervention. A challenge in designing POC trials is obtaining sufficient information to make this important go/no-go decision in a cost-effective manner. An IMMPACT consensus meeting was convened to discuss design considerations for POC trials in analgesia, with a focus on maximizing power with limited resources and participants. We present general design aspects to consider including patient population, active comparators and placebos, study power, pharmacokinetic-pharmacodynamic relationships, and minimization of missing data. Efficiency of single-dose studies for treatments with rapid onset is discussed. The trade-off between parallel-group and crossover designs with respect to overall sample sizes, trial duration, and applicability is summarized. The advantages and disadvantages of more recent trial designs, including N-of-1 designs, enriched designs, adaptive designs, and sequential parallel comparison designs, are summarized, and recommendations for consideration are provided. More attention to identifying efficient yet powerful designs for POC clinical trials of chronic pain treatments may increase the percentage of truly efficacious pain treatments that are advanced to confirmatory trials while decreasing the percentage of ineffective treatments that continue to be evaluated rather than abandoned

Core outcome measures for opioid abuse liability laboratory assessment studies in humans: IMMPACT recommendations

A critical component in development of opioid analgesics is assessment of their abuse liability (AL). Standardization of approaches and measures used in assessing AL have the potential to facilitate comparisons across studies, research laboratories, and drugs. The goal of this report is to provide consensus recommendations regarding core outcome measures for assessing the abuse potential of opioid medications in humans in a controlled laboratory setting. Although many of the recommended measures are appropriate for assessing the AL of medications from other drug classes, the focus here is on opioid medications because they present unique risks from both physiological (e.g., respiratory depression, physical dependence) and public health (e.g., individuals in pain) perspectives. A brief historical perspective on AL testing is provided, and those measures that can be considered primary and secondary outcomes and possible additional outcomes in AL assessment are then discussed. These outcome measures include the following: subjective effects (some of which comprise the primary outcome measures, including drug liking; physiological responses; drug self-administration behavior; and cognitive and psychomotor performance. Before presenting recommendations for standardized approaches and measures to be used in AL assessments, the appropriateness of using these measures in clinical trials with patients in pain is discussed