Sinecatechins

drug
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Also known as Camellia sinensis catechinsCamellia sinensis leaf catechinsKunecatechinsPolyphenon eVeregen

Summary

Sinecatechins (CHEMBL1201723) is an approved unknown (ATC D06BB12); indicated across 4 conditions including viral infectious disease and basal cell carcinoma.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Unknown
  • ATC class: D06BB12
  • Indications: 4 conditions
  • Clinical trials: 17

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201723
NameSinecatechins
TypeUnknown
Max phase4
ATCD06BB12

Also known as: Camellia sinensis catechins, Camellia sinensis leaf catechins, Kunecatechins, Polyphenon e, Sinecatechins, Veregen, SINECATECHINS

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

4 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
viral infectious disease4MONDO:0005108EFO:0000763
basal cell carcinoma2MONDO:0020804EFO:0004193
prostate carcinoma2MONDO:0005159EFO:0001663
anogenital human papillomavirus infection1MONDO:0005647EFO:0007147

Clinical trials

Total trials: 17.

Phase distribution

PhaseTrials
PHASE28
PHASE14
PHASE41
PHASE2/PHASE31
PHASE31
PHASE1/PHASE21
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02622568PHASE4COMPLETEDInvestigating Veregen ™ 15% Ointment Treatment For Non-facial Verrucae in Pediatric Patients: A Pilot Study
NCT02029352PHASE2/PHASE3COMPLETEDTopical Green Tea Ointment in Treatment of Superficial Skin Cancer
NCT04055142PHASE3COMPLETEDClinical Trial for Evaluating the Efficacy and Safety of Electrocoagulation vs Topic Sinecatechins vs Topic Cidofovir Within the Treatment to High-grade Anal Intraepithelial Neoplasia in HIV Homosexual Males
NCT04597359PHASE2ACTIVE_NOT_RECRUITINGTo Evaluate if Green Tea Can be Effective in Reducing the Progression of Prostate Cancer in Men on Close Monitoring
NCT00005097PHASE2TERMINATEDGreen Tea Extract in Treating Patients With Actinic Keratosis
NCT00088946PHASE2COMPLETEDErlotinib and Green Tea Extract (Polyphenon® E) in Preventing Cancer Recurrence in Former Smokers Who Have Undergone Surgery for Bladder Cancer
NCT00262743PHASE1/PHASE2COMPLETEDGreen Tea Extract in Treating Patients With Stage 0, Stage I, or Stage II Chronic Lymphocytic Leukemia
NCT00363805PHASE2COMPLETEDGreen Tea or Polyphenon E in Preventing Lung Cancer in Former Smokers With Chronic Obstructive Pulmonary Disease
NCT00596011PHASE2COMPLETEDStudy of Polyphenon E in Men With High-grade Prostatic Intraepithelial Neoplasia
NCT00676793PHASE2COMPLETEDA Study of the Effect of Polyphenon E (Green Tea Extract) on Breast Cancer Progression
NCT01060345PHASE2TERMINATEDA Pilot Study of Chemo-prevention of Green Tea in Women With Ductal Carcinoma in Situ
NCT01451723PHASE2TERMINATEDSafety and Neuroprotective Effects of Polyphenon E in MS; Phase II
NCT00707252PHASE1TERMINATEDStudy of Polyphenon E in Addition to Erlotinib in Advanced Non Small Cell Lung Cancer
NCT00836719PHASE1COMPLETEDSafety of Polyphenon E in Multiple Sclerosis Pilot Study
NCT01433289PHASE1COMPLETEDStudy to Evaluate Safety and Toxicity of Polyphenon E (EGCG) in HIV-1-Infected Individuals
NCT01490008PHASE1COMPLETEDSystemic Exposure of Catechins From Veregen 15% Ointment in Patients With External Anogenital Warts and From Oral Intake of Green Tea Beverage in Healthy Volunteers
NCT02147353Not specifiedCOMPLETEDTreatment of External Genital Warts With Cryotherapy and Sinecatechins 15% Ointment

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).