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Now enrolling adults with type 1 diabetes for a nighttime hypoglycemia study.

T1D Exchange is helping Zucara Therapeutics recruit for their Phase 2 clinical trial evaluating an investigational drug that may help adults living with type 1 diabetes (T1D) who experience nighttime lows.

New study locations have recently been added across the U.S., making participation easier. If you live near one of the following locations, you may now be eligible for this clinical trial, even if you were previously disqualified.

T1D Exchange is not a sponsor and is not administering this clinical trial, nor are we implying that you will qualify. We are sharing this research opportunity with you so you can decide whether to seek more information or participate.

See if You Qualify
Zucara Study

CLINICAL TRIAL DETAILS

Zucara Therapeutics, Inc., is conducting a clinical trial to evaluate an investigational medication that may lower the risk of experiencing low glucose levels during the night.
This clinical trial will help determine how well ZT-01, an investigational drug, works in reducing nighttime hypoglycemia and the safety and tolerability of three dose levels of ZT-01 in adults with T1D.

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ELIGIBILITY CRITERIA

Zucara Therapeutics is looking for individuals who:

  • Are between the ages of 18 to 75
  • Have lived with T1D for at least five years
  • Have recently experienced low glucose levels during the night.

* The guidelines listed above are the primary eligibility criteria for this study. Only the clinical trial research staff can determine if you meet all eligibility criteria for this study.

See if you qualify

Step 1: Complete a brief questionnaire to determine if you may be a good fit for this
clinical trial.
Step 2: If your answers in the eligibility screener suggest you may qualify, your local
study site coordinator will contact you. Your local study site coordinator will ask follow-
up questions to confirm your eligibility for this clinical trial. They will also provide
additional information about this research opportunity and, if you qualify, give you the
option to enroll.
See if You Qualify

To protect your privacy, we will not share your contact information with the study staff unless you sign the Informed Consent Form at the beginning of the eligibility questionnaire.

DIRECTORY OF SITES BY STATE

University of Southern California
Keck School of Medicine
Eastside Center for Diabetes

245 South Fetterly Ave
Suite 22
Los Angeles, CA 90022

Headlands Research- AMCR Institute

625 West Citracado Parkway
Escondido, CA 92025

Hanson Clinical Research Center Inc.

21216 Olean Blvd, Suite 6 & 7
Port Charlotte, FL 33952

Palm Beach Diabetes and Endocrine Specialists
Metabolic Research Institute

1515 North Flagler Dr
Suite 440
West Palm Beach, FL 33401

East Coast Institute for Research

8773 Perimeter Park Court
Jacksonville, FL 32216

East Coast Institute for Research

265 Sheraton Blvd, Suite 100
Macon, GA 31210

Indiana Health University Hospital

550 North University Blvd
Indianapolis, IN 46202

MedStar Good Samaritan Hospital

5601 Loch Raven Blvd, 2nd floor
Baltimore, MD 21239

Palm Medical Group / Palm Research Centre Inc

9280 West Sunset Rd
Suite 306
Las Vegas, NV 89148

Albany Medical Center – Albany Med Endocrinology

220 Washington Avenue Ext
Albany, NY 12203

Lucas Research, Inc.

623 North 35th Street
Morehead City, NC 28557

University Diabetes & Endocrine Consultants

5616 Brainerd Rd
Suite 208
Chattanooga, TN 37411

Texas Diabetes and Endocrinology – South Austin Office

5000 Davis Lane
Suite 200
Austin, TX 78749

Diabetes & Glandular Disease Clinic

5107 Medical Dr
San Antonio, TX 78229

Southern Endocrinology Associates

1621 North Belt Line Road
Suite A
Mesquite, TX 75149

North Texas Endocrine Center

9301 North Central Expressway
Suite 570, Tower II
Dallas, TX 75231

Diabetes & Endocrine Treatment Specialists

7410 S. Creek Road
Suite 100
Sandy, UT 84093

NOTE: This site is for US residents only. If you do not live in the United States and are located in Canada, please click on this link to learn more about how you may be able to participate in this trial.

WHAT TO EXPECT IF YOU ENROLL IN THE CLINICAL TRIAL

  • Participation in the clinical trial will last approximately 16 weeks. During the trial, participants take subcutaneous injections with at least two weeks of no injections.
  • The study requires six in-person visits and two phone calls over this period – approximately 16 weeks.
  • The clinical trial research staff will communicate other requirements.
  • Qualified participants will receive payment for time and travel.
See if You Qualify
Zucara Study 2
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