Optimizing Social Utility in Sequential Experiments

arXiv:2605.06520 · cs.GT, cs.LG, cs.MA, stat.ME · Submitted 2026-05-07 · Read on arXiv

cs.GT, cs.LG, cs.MA, stat.ME

Submitted: 2026-05-07

Updated: 2026-10-17

Comments: NeurIPS 2026

License: http://creativecommons.org/licenses/by/4.0/

The gist: Regulatory approval of products in high-stakes domains such as drug development requires statistical evidence of safety and efficacy through large-scale randomized controlled trials.

Abstract

Regulatory approval of products in high-stakes domains such as drug development requires statistical evidence of safety and efficacy through large-scale randomized controlled trials. However, the high financial cost of these trials may deter developers who lack absolute certainty in their product's efficacy, ultimately stifling the development of `moonshot' products that could offer high social utility. To address this inefficiency, in this paper, we introduce a statistical protocol for experimentation where the product developer (the agent) conducts a randomized controlled trial sequentially and the regulator (the principal) partially subsidizes its cost. By modeling the protocol using a belief Markov decision process, we show that the agent's optimal strategy can be found efficiently using dynamic programming. Further, we show that the social utility is a piecewise linear and convex function over the subsidy level the principal selects, and thus the socially optimal subsidy can also be found efficiently using divide-and-conquer. Simulation experiments using publicly available data on antibiotic development and approval demonstrate that our statistical protocol can be used to increase social utility by more than 35 % relative to standard, non-sequential protocols.

Related papers