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Paper
Emulating Randomized Controlled Trials with Hybrid Control Arms in Oncology: A Case Study
A Comparison of 7 Oncology External Control Arm Case Studies: Critiques From Regulatory and Health Technology Assessment Agencies
Characterizing RWD Quality and Relevancy for Regulatory Purposes
CONSORT extension for the reporting of randomised controlled trials conducted using cohorts and routinely collected data (CONSORT-ROUTINE): checklist with explanation and elaboration
Super-covariates: Using predicted control group outcome as a covariate in randomized clinical trials
Dynamic use of historical controls in clinical trials for rare disease research: a re-evaluation of the MILES trial
Bayesian Prognostic Covariate Adjustment With Additive Mixture Priors
A Structured Preapproval and Postapproval Comparative Study Design Framework to Generate Valid and Transparent Real-World Evidence for Regulatory Decisions
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