ClinicalTrials.gg
Not yet recruitingNCT07585630Updated May 18, 2026

A1Cantus vs. Placebo

A Phase 2 interventional study of A1C Drink and Placebo drink in Type 2 Diabetes, sponsored by University of California, Riverside. Not yet recruiting at 1 site in United States. Open to participants aged 21 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-18.

Sponsored by University of California, Riverside · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
21 Years to 75 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 3,304 studies in Diabetes Mellitus, Type 2 with a site in United States — 344 open to participants now, 478 under way, 51 of them phase 3. Diabetes Mellitus, Type 2 · United States.

Planned enrollment
1,865th of 2,957
50 · median 90
Started
2026
with 152 others
Phase 2
391 of 3,304
25 open now
Primary completion
2027-12
later than 326 of 476 live
Registered
3,232nd of 3,304
by date

Among the 3,304 studies in Diabetes Mellitus, Type 2 with a site in United States, this one is the 1,865th largest by planned enrollment of the 2,957 interventional ones that give a count, is one of 153 that started in 2026, is one of 391 in phase 2, reaches primary completion later than 326 of the 476 other live ones, and was the 3,232nd registered.

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

Browse Diabetes Mellitus, Type 2 studies →

Open to participants now

344 of the 3,304 studies in Diabetes Mellitus, Type 2 with a site in United States are open now. Recruiting first, the newest first:

339 more — sign in →

All 344 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 883 Diabetes Mellitus, Type 2 studies recruiting now, 373 (42%) set no upper age limit and 384 (43%) stop at 75 or younger; 52 take children under 18; 203 take healthy volunteers.

This study: 21 Years to 75 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 3,304 studies in Diabetes Mellitus, Type 2 with a site in United States, or all of them as a file.
02

Study summary

The investigators will conduct a randomized controlled 2-arm parallel trial of A1c Drink vs. Placebo over a 3-month period and compare changes in Ha1c from baseline to 3 months. Investigator and study personnel, as well as participants, will be blinded to drink assignments.

03

Conditions studied

  • Type 2 Diabetes
04

Who can participate

Ages eligible
21 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults 21 years of age or older and not older than 75 recruited from UCR Health
  • Clinical diagnosis of type II DM with Ha1c >= 8 but less than or equal to 10
  • Stable medications for at least 6 months
  • Speak Spanish and/or English
  • Sign an form
  • No other members in their household are participating in the study

Exclusion criteria

Exclusion Criteria:

  • Patients \<21 years of age, who do not have type II DM, whose Ha1c is less than 8 or > 10,
  • Have major complications of diabetes, including CKD, diabetic retinopathy, ADVD risk > 5, or history of CVD/stroke
  • Do not speak and understand either English or Spanish well
  • Allergic to cinnamon
  • Severe diseases, such as cancer
  • Compromised immune system
  • Eating disorders
  • of 40 or higher
  • Already have a family member participating in the study
  • Substance use disorder
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Placebo comparator
    Placebo Drink

    The placebo drink will be formulated to closely match the active drink in taste, color and mouthfeel, while removing all active ingredients.

    Other: Placebo drink

  • Experimental
    A1C Drink

    The A1C drink is currently on the market with natural active ingredients.

    Dietary Supplement: A1C Drink

Interventions

  • Dietary supplementA1C Drink

    In the experimental arm, participants will drink the A1C drink BID for 3 months as instructed. Both the active and placebo drinks will be identical in can size (12 oz slim can), packaging format, and visual appearance.

  • OtherPlacebo drink

    In the placebo arm, participants will drink the placebo drink BID for 3 months as instructed. Both the active and placebo drinks will be identical in can size (12 oz slim can), packaging format, and visual appearance.

06

What researchers measure

Primary outcomes

  1. Hemoglobin A1C

    Change in Ha1c from baseline to 3 months. To test the efficacy of the A1Cantus drink in improving glycemic control in patients with Type II Diabetes

    Time frame: 3 months

Secondary outcomes

  1. Change in A1C

    Percentage of participants whose A1C was lowered from Baseline to 3 months

    Time frame: 3 months

  2. Hypertension

    Change in systolic and diastolic blood pressure from baseline to three months

    Time frame: 3 months

  3. Body Mass Index (BMI)

    Change in body mass index from baseline to 3 months

    Time frame: 3 months

  4. Cholesterol

    Change in fasting LDL and HDL from baseline to three months

    Time frame: 3 months

07

Study locations

1 site
  • UCR Health
    Riverside, California 92521, United States
08

References and documents

Publications

  • Centers for Disease Control and Prevention. (2026) National Diabetes Statistics Report, 11 Mar 2026. Available at https://gis.cdc.gov/grasp/diabetes/diabetesatlas-statsreport.html.
  • Lorestanifar M, Mosayebi Molasaraei M, Jashaninejad R, Khoshmanesh S, Doosti-Irani A. The prevalence of uncontrolled diabetes mellitus in patients with type 2 diabetes: a multicenter cross-sectional study. J Diabetes Metab Disord. 2023 Mar 17;22(1):787-792. doi: 10.1007/s40200-023-01201-9. eCollection 2023 Jun. PubMed 37255779 ↗
  • https://diabetes.org/about-diabetes/complications

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jun 2026; primary completion for Dec 2027, 18 months later.

Of 99 non-industry phase 2 interventional studies under Diabetes Mellitus, Type 2, half reached primary completion within 34 months of starting (the median), counting those still running; a quarter within 16 and three quarters within 50. This study's planned 18 months is below that.

Counting every sponsor, half of 293 studies reached it within 15 months; a quarter within 11 and three quarters within 27.

How these figures are worked out, and which studies are left out of them.

Registered
May 7, 2026
First posted
May 14, 2026
StartEst.
Jun 15, 2026
Primary completionEst.
Dec 15, 2027
CompletionEst.
Jun 1, 2028
Last update
May 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07585630
Lead sponsor
University of California, Riverside
Collaborators
A1Cantus
Responsible party
Sponsor
First posted
May 14, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Dec 15, 2027 (estimated)
Completion
Jun 1, 2028 (estimated)
Last update
May 18, 2026

Study contacts

Elizabeth Jacobs, MD, MPP
Contact
elizabeth.jacobs@medsch.ucr.edu
951-827-8643

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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