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NCT03463018

Echinacea Angustifolia (AnxioCalm) in Anxiety

Terminated Phase 2 Last updated 24 March 2022
What this trial tests

Phase 2 trial testing Echinacea angustifolia in Generalized Anxiety Disorder in 100 participants. Terminated before completion.

Timeline
6 June 2018
Primary endpoint
3 October 2020
15 December 2021

Quick facts

Lead sponsorEuroPharma, Inc.
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment100
Start date6 June 2018
Primary completion3 October 2020
Estimated completion15 December 2021
Sites1 location across Georgia

Drugs / interventions tested

Conditions studied

Sponsor

EuroPharma, Inc.

Who can join

18 and older, any sex, with Generalized Anxiety Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates whether Echinacea angustifolia (AnxioCalm) is a safe and effective treatment for mild to moderate Generalized Anxiety Disorder (GAD) symptoms. Half the participants will receive Echinacea angustifolia and half will receive placebo.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Generalized Anxiety Disorder

Currently open trials in the same condition.

Other EuroPharma, Inc. 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/NCT03463018.

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