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. 2015 Jun 1;80(4):740–749. doi: 10.1111/bcp.12646

Table 2.

Effect of partially informative vs. non-informative prior

Prior Relative risk of uterine quiescence Difference in time to delivery
Partially informative prior using data from phase 2 dose-ranging study 1.53 (95% CrI 0.98, 2.48) 8.2 (95% CrI 2.7, 13.74)
Non-informative prior (phase 2a proof of concept study only) 1.54 (95% CrI 0.94, 2.63) 7.3 (95% CrI 1.0, 13.5)

CrI, credible interval.