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NCT05428215

Comparison of PKs of 17-Beta-Estradiol Via Sublingual Placement Versus Swallowing in Male-to-Female Transgender Patients

Terminated Phase 4 Last updated 27 July 2023
What this trial tests

Phase 4 trial testing 17beta Estradiol in Gender Dysphoria in 2 participants. Terminated before completion.

Timeline
29 December 2022
Primary endpoint
20 July 2023
20 July 2023

Quick facts

Lead sponsorMaineHealth
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposetreatment
Enrollment2
Start date29 December 2022
Primary completion20 July 2023
Estimated completion20 July 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

MaineHealth — full company profile →

Who can join

18 and older, male only, with Gender Dysphoria. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This crossover study will investigate the pharmacokinetics of oral versus sublingual administration of 17-beta-estradiol in the trans-female population.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of 17beta Estradiol

Trials testing the same drug.

Other recruiting trials for Gender Dysphoria

Currently open trials in the same condition.

Other MaineHealth trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05428215.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing