Drugs / Oxybenzone
last change Dec 2021 re-read 9 days ago

Oxybenzone

Developed for
radiation-induced disorder
Investigated by
Food and Drug Administration (FDA) · Spaulding Clinical Research LLC · Yale University

Regulatory milestones approvals, filings & regulatory actions · 1 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Approved US (FDA) SHADE UVAGUARD — 1992-12-07 fda.gov ↗

Trials 2

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT03582215 Jul 2018 → Feb 2019 skin sensitivity to sun Food and Drug Administration (FDA) Completed No outcome recorded
Phase 1 NCT02668536 Jul → Aug 2017 melanoma, radiation-induced disorder Yale University Completed No outcome recorded
Comparator or background therapy3 trials
— NCT05124899 Comparator Nov → Dec 2021 — HALEON Completed No outcome recorded
— NCT05109104 Comparator Nov → Dec 2021 — HALEON Completed No outcome recorded
— NCT05085327 Comparator Oct → Nov 2021 — HALEON Completed No outcome recorded

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as Oxybenzone “Areas will be treated with a standard preparation, consisting of padimate O (7%) and oxybenzone (3%) will be used as the control sunscreen.” NCT02668536 ↗
4

“SPF Standard (7 percent \[%\] Padimate-O and 3% Oxybenzone)” NCT05109104 ↗

“SPF Standard (7 percent [%] Padimate-O and 3% Oxybenzone)” NCT05124899 ↗

“Ingredients: 3% Avobenzone; 4% Oxybenzone; 6% Octocrylene” NCT03582215 ↗

“Padimate-O and 3% Oxybenzone” NCT05085327 ↗

Route Topical “Single topical application” NCT05085327 ↗