Seeking Volunteers With Type 2 Diabetes Who Treat with Oral Diabetes Medications.

Updated on 22 October 2021
type 2 diabetes mellitus
hemoglobin a1c
type 2 diabetes
finger stick
diabetes type 2


We are currently seeking volunteers who are diagnosed with Type 2 Diabetes and who are treating with at least one and up to three oral diabetes medications, including any of the following:
  • Metformin
  • DPP-4 inhibitors (Januvia, Onglyza, Tradjenta, or Nesina.)
  • SLGT-2 inhibitors (Farxiga, Invokana, or Jardiance.)
  • TZDs (Avandia, Actos, or Rezulin.)
  • Sulfonylureas (Glyburide, Glipizide, or Glimepiride.)
This is a study of an investigational oral insulin that may help improve blood sugar levels. All participants will continue their current medications and will go into 1 of 3 different groups: two out of every three participants will take the investigational medication; one out of every three will take a placebo. Participants must be willing to keep a daily diary: (ie, hypo’s and finger sticks [value/date/time]), and wear a CGM on three separate occasions for 10 days each.


The study period is 57 weeks and will require 14 clinic visits.
Participants will receive at no cost: study medication, study-related: physical exams, EKG’s, lab work, a glucose meter, test strips and other supplies. In addition, participants will be compensated up to $1050 for completion of the study ($75 per visit). Participants will receive payment on a quarterly basis.

Condition Diabetes Mellitus Type 2, Diabetes (Pediatric), Diabetes Prevention, Diabetes Mellitus Types I and II, Diabetes Mellitus, Type 2
Clinical Study IdentifierTX264013
Last Modified on22 October 2021


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Inclusion Criteria

Must have been diagnosed with Type 2 Diabetes for at least 6 months
Must have an HbA1c between 7.5 - 11.0% at screening
Must have a BMI between 25 - 40
Must meet other eligibility criteria. Please contact us for further details
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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