Page contentsPage contents Key facts Decision Key facts Active substance resiquimod Therapeutic area Neoplasms benign, malignant and unspecified (incl cysts and polyps) Decision number EMA/PE/0000181238 PIP number EMA/PE/0000181238 Pharmaceutical form(s) Solution for infusion Condition(s) / indication(s) Treatment of melanoma Route(s) of administration Intravenous use Contact for public enquiries Eikon Therapeutics Inc.Email: vangalas@eikontx.comTel: +1 3417770566 Decision type P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s) Decision date 06/12/2024 Compliance check done No Decision EMA/PE/0000181238: EMA decision of 6 December 2024 on the agreement of a paediatric investigation plan and on the granting of a waiver for resiquimodAdopted Reference Number: EMADOC-1700519818-1775491 English (EN) (215.47 KB - PDF)First published: 17/12/2025 View Share this page