Our editorial approach
We compile information about company programs, registries, public filings, and peer-reviewed literature, emphasizing transparency about sources and limits. When we assert the regulatory status of a program we link to primary documents or registries; for example, industry registries and trial records are consulted alongside literature and regulator statements from established portals such as Wikipedia's clinical trial overview and authoritative registries hosted by government agencies.
Information is organized to be evidence-first: claims are tied to documents, and we flag where data are preliminary or promotional.
How information is sourced
Our editors prioritize primary sources: trial registries, company filings, regulatory notices, and peer-reviewed publications. In cases where registry data are sparse, we describe the provenance of promotional statements and seek corroboration via academic databases and official public notices such as those maintained by the U.S. Food and Drug Administration.
We also monitor public conversations around development programs; for context on community reporting and patient narratives we review open forums and community sites as part of a broader evidence map, which can include threads on community platforms like ibogainereddit discussions when those conversations illuminate real-world questions (always marked as anecdotal).