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RECRUITING
NCT05762107
PHASE2

A Study of the Effect of ZT-01 on Night-time Hypoglycemia in Type 1 Diabetes

Sponsor: Zucara Therapeutics Inc.

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn about the effect of the study drug (ZT-01) on low blood sugar (hypoglycemia) in adults with type 1 diabetes (T1D) who have been having low blood sugars ("hypos") at night. ZT-01 increases the amount of a hormone called glucagon during low blood sugar, and this may help prevent the occurrence of hypos. The main questions this trial aims to answer are whether ZT-01 lowers the number of hypos happening at night, and what its effects are on blood sugar levels. The safety of ZT-01 will also be measured. Participants will be asked to wear a study-provided continuous glucose monitor (CGM) during two 4-week periods when they will self-inject the study drug before bed. They will get ZT-01 at one of three dose levels during one period, and placebo (which looks like the study drug but doesn't contain the active ingredient) during the other. Neither the participant nor the study site will know what they are receiving during each treatment period or see data from the CGM. The participant will continue to use their usual methods of measuring blood sugar (including their personal CGM) and giving insulin during the study. The participant will be asked to complete a short diary each evening, and will be asked to upload the CGM data to a study phone every day. If a participant uses their own CGM and is willing to share information on how often they have low blood sugar with the study site at the first visit to see if they meet study entry requirements, they will have 6 study visits, 2 study phone calls, and be in the study for about 16 weeks. If they don't use CGM or don't want to share their information, then they will be asked to wear a study CGM for an extra 4 weeks to find out how many low blood sugars they have, and will have an extra visit. Study participants will be asked to give blood and urine for testing to see whether they meet the requirements to enter the study, and at the start and end of each treatment period to see if the study treatment has any effects. They will also have their blood pressure and temperature taken at each study visit, and have an ECG at 4 visits to measure the electrical activity of their heart. Some participants will be asked to also take part in a sub-study where their blood level of ZT-01 and glucagon is measured, after the first and last dose. They will be asked to stay at the study site overnight for each set of measurements (4 in total).

Official title: A Phase 2a Randomized, Double-blind, Placebo-controlled, Multiple-dose, Crossover Study of the Effect of ZT-01 on Frequency of Nocturnal Hypoglycemia in Type 1 Diabetes Mellitus

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

186

Start Date

2023-07-28

Completion Date

2027-05

Last Updated

2025-12-04

Healthy Volunteers

No

Interventions

DRUG

Placebo

Subject receives Placebo by subcutaneous injection daily for 28 days

DRUG

ZT-01, 7 mg

Subject receives ZT-01 7 mg by subcutaneous injection daily for 28 days

DRUG

ZT-01, 15 mg

Subject receives ZT-01 15 mg by subcutaneous injection daily for 28 days

DRUG

ZT-01, 22 mg

Subject receives ZT-01 22 mg by subcutaneous injection daily for 28 days

Locations (33)

Headlands Research

Escondido, California, United States

USC Keck Medicine Eastside Center for Diabetes

Los Angeles, California, United States

LCGK Research

San Carlos, California, United States

East Coast Institute for Research LLC

Jacksonville, Florida, United States

Suncoast Clinical Research

New Port Richey, Florida, United States

Hanson Diabetes Center

Port Charlotte, Florida, United States

Metabolic Research Institute

West Palm Beach, Florida, United States

Atlanta Diabetes Associates

Atlanta, Georgia, United States

Physicians Research Associates LLC

Lawrenceville, Georgia, United States

East Coast Institute for Research

Macon, Georgia, United States

IU Health University Hospital

Indianapolis, Indiana, United States

University of Kansas Medical Center

Kansas City, Kansas, United States

Baltimore VA Medical Center

Baltimore, Maryland, United States

MedStar Good Samaritan Hospital

Baltimore, Maryland, United States

Elite Research Center

Flint, Michigan, United States

Palm Research Center, Inc.

Las Vegas, Nevada, United States

Albany Medical Center

Albany, New York, United States

NYC Research Inc.

Long Island City, New York, United States

Lucas Research Inc.

Morehead City, North Carolina, United States

Thomas Jefferson University

Philadelphia, Pennsylvania, United States

University Diabetes & Endocrine Consultants

Chattanooga, Tennessee, United States

Texas Diabetes & Endocrinology, PA

Austin, Texas, United States

North Texas Endocrine Center

Dallas, Texas, United States

Southern Endocrinology Associates

Mesquite, Texas, United States

Diabetes & Glandular Disease Clinic

San Antonio, Texas, United States

Diabetes & Endocrine Treatment Specialists

Sandy City, Utah, United States

Centricity Research Calgary Endocrinology

Calgary, Alberta, Canada

BC Diabetes

Vancouver, British Columbia, Canada

Centricity Research Barrie Endocrinology

Barrie, Ontario, Canada

Centricity Research Vaughan Endocrinology

Concord, Ontario, Canada

Centricity Research Etobicoke Endocrinology

Etobicoke, Ontario, Canada

Centricity Research Toronto

Toronto, Ontario, Canada

Mount Sinai Hospital: Leadership Sinai Centre for Diabetes

Toronto, Ontario, Canada