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epigallocatechin-3-gallate

Phase 2

Huntington Disease | Small molecule | Neurology |Pulmonx Corporation|Last Updated: Jun 16, 2015

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment54

FDA Designations

No designations recorded

Clinical trial landscape

epigallocatechin-3-gallate · 1 trial · 1 indication

Phase 2 1
NCT01357681Effects of EGCG (Epigallocatechin Gallate) in Huntington's Disease (ETON-Study)Huntington Disease
COMPLETED54 Analytics
PHASE2COMPLETED
Effects of EGCG (Epigallocatechin Gallate) in Huntington's Disease (ETON-Study)
Huntington DiseaseUnlock trial analytics

Study Endpoints

Primary Endpoints

Change of cognitive functions (UHDRS-Cognition: composite score of Stroop test, Verbal fluency & Symbol Digit Modalities Test) after 12 months in comparison to baseline
Month 0, Month 12

Secondary Endpoints

UHDRS Motor Score
Month 0, Month 12
UHDRS Behavioural Score
Month 0, Month 12
UHDRS Functional Assessment
Month 0, Month 12
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
(2)-epigallocatechin-3-gallate (EGCG)EXPERIMENTALMonth 01:400 mg /day (200-0-200) p.o. Month 02:800 mg /day (400-0-400) p.o. Month 03 -12: 1200 mg /day (600-0-600) p.o.
PlaceboPLACEBO_COMPARATORPlacebo

Interventions

NameTypeDescription
(2)-epigallocatechin-3-gallate (EGCG)DRUGMonth 01:400 mg /day (200-0-200) Month 02:800 mg /day (400-0-400) Month 03 -12: 1200 mg /day (600-0-600)
PlaceboDRUGPlacebo
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites3

Inclusion Criteria: * Chorea Huntington (CAG repeats \>39) * UHDRS TFC \>5 * ≥18 years of age * Readiness and ability to take oral medication * Normal liver function laboratory test * Stable concomitant medication regimen \> 4 weeks prior to Baseline * Motivation for women with childbearing potenti...

Countries:Germany
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Competitive Landscape -Huntington's Disease 8 trials (matched to "Huntington Disease")

Frequently asked questions about epigallocatechin-3-gallate

What is epigallocatechin-3-gallate used for?

Epigallocatechin-3-gallate is an investigational small molecule being studied for the treatment of Huntington disease. It is currently in Phase 2 clinical development. The drug has been evaluated in a completed clinical trial with 54 participants, but it is not yet approved for any use.

Who is developing epigallocatechin-3-gallate?

Pulmonx Corporation, traded on the NASDAQ under the ticker LUNG, is developing epigallocatechin-3-gallate. The company is conducting clinical research on this drug for Huntington disease, a neurological condition. The drug is currently in Phase 2 development.

What phase is epigallocatechin-3-gallate in?

Epigallocatechin-3-gallate is in Phase 2 clinical development for Huntington disease. It is an investigational drug, meaning it has not been approved by regulatory authorities. The drug has completed one Phase 2 trial, and no active trials are currently listed for this asset.

What clinical trials has epigallocatechin-3-gallate been in?

Epigallocatechin-3-gallate has been studied in one completed clinical trial, identified as NCT01357681. This Phase 2 study, titled "Effects of EGCG (Epigallocatechin Gallate) in Huntington's Disease (ETON-Study)," enrolled 54 participants in Germany. The trial was randomized, double-blind, and placebo-controlled, and it included biomarker selection.

Is epigallocatechin-3-gallate the same as EGCG?

Yes, epigallocatechin-3-gallate is also known as EGCG. The clinical trial NCT01357681, which studied this drug in Huntington disease, used the abbreviation EGCG in its title. The drug is a small molecule being developed by Pulmonx Corporation for this neurological condition.