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Completed Phase 2 Interventional

A Phase 2 Study of Cyclo-Z in Subjects With Type 2 Diabetes

ClinicalTrials.gov ID: NCT03560271

Public ClinicalTrials.gov record NCT03560271. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 6:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase 2 Study to Evaluate the Efficacy and Safety of Cyclo-Z in Subjects With Type 2 Diabetes

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a double-blind, randomized, placebo-controlled, parallel-group comparison study to evaluate the efficacy and safety of Cyclo-Z vs. placebo in adult subjects with type 2 diabetes. Approximately 20 clinical sites may be utilized in the United States so that approximately 300 subjects (a potential 20% screening failure rate) may be screened for total 28-week study period (2 weeks for screening, 24 weeks for treatment, and 2 weeks for safety follow-up).

Study identification

NCT ID
NCT03560271
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NovMetaPharma Co., Ltd.
Industry
Enrollment
256 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 17, 2018
Primary completion
Jun 24, 2019
Completion
Jul 14, 2019
Last update posted
Nov 17, 2019

2018 – 2019

United States locations

U.S. sites
20
U.S. states
9
U.S. cities
19
Facility City State ZIP Site status
Study Site 29 Anniston Alabama 36207
Study Site 26 Birmingham Alabama 35216
Study Site 27 Chula Vista California 91911
Study Site 28 La Mesa California 91942
Study Site 10 Montclair California 91763
Study Site 23 North Hollywood California 91606
Study Site 13 Coral Gables Florida 33134
Study Site 19 DeLand Florida 32720
Study Site 14 Miami Florida 33155
Study Site 12 Miami Beach Florida 33140
Study Site 15 Orlando Florida 32806
Study Site 16 St. Petersburg Florida 33711
Study Site 21 Peachtree Corners Georgia 30071
Study Site 17 Snellville Georgia 30078
Study Site 20 North Dartmouth Massachusetts 02747
Study Site 30 Caro Michigan 48723
Study Site 24 Las Vegas Nevada 89106
Study Site 18 Cleveland Ohio 44142
Study Site 22 San Antonio Texas 78220
Study Site 11 San Antonio Texas 78249

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03560271, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 17, 2019 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03560271 live on ClinicalTrials.gov.

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