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NCT07367061

Clinical Investigation to Assess Safety and Efficacy of INNEA AQUA in Adult Women With Vulvo-Vaginal Atrophy (VVA)

Active, enrolled NA Last updated 9 February 2026
What this trial tests

NA trial testing product: Innea Aqua vaginal use in Vulvo Vaginal Atrophy in 62 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
25 September 2025
Primary endpoint
30 May 2026
30 June 2026

Quick facts

Lead sponsorInnate srl
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment62
Start date25 September 2025
Primary completion30 May 2026
Estimated completion30 June 2026
Sites3 locations across Romania

Drugs / interventions tested

Conditions studied

Sponsor

Innate srl

Who can join

Adults 18 to 75, female only, with Vulvo Vaginal Atrophy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Clinical investigation to assess safety and efficacy of INNEA AQUA in adult women with Vulvo-Vaginal Atrophy (VVA). To assess the Safety and efficacy of INNEA AQUA

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Innate srl trials

Trials by the same sponsor.

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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/NCT07367061.

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