Process development to overcome drug substance agglomeration and restore dissolution performance.
Singhal M; Nidadavole K; Murphy DS; Kalaria D · 2026 · Journal of pharmaceutical sciences
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Dissolution testing is performed to understand the rate and extent of drug release for assurance of in vivo bioavailability. In this case study, an immediate-release tablet of an investigational BCS Class II compound exhibited slow and…
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Metadata source: Europe PMC · DOI 10.1016/j.xphs.2026.104368