ClinicalTrials.gg
Active, not recruitingNCT07340320Updated Nov 10, 2026

A Study of CX11 Tablets in Patients With Type 2 Diabetes Mellitus

A Phase 2 interventional study of CX11 and Placebo in Type II Diabetes Mellitus, sponsored by Corxel Pharmaceuticals. Active, not recruiting at 44 sites in 2 countries. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Corxel Pharmaceuticals · Phase 2, Interventional, and Treatment

Updated Nov 10, 2026Now Active, not recruitingPrimary completion moved+3 moreGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
251
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study is testing whether a new medication called CX11 works and is safe for participants with type 2 diabetes who have not reached good blood sugar control while taking a steady dose of metformin, with or without a steady dose of an SGLT2 inhibitor, for at least 90 days.

The study is being done at multiple medical centers. Participants are assigned by chance (randomized) to different groups, and neither the participants nor the study staff know which group they're in (double-blind). The groups are compared side by side (parallel), and some participants will receive inactive pills (placebo) to help measure the true effect of the study drug.

After screening, participants will be randomly placed into one of six groups, with equal chances of being in any group. Each group will receive a different dose of CX11 or a placebo. Treatment will last 24 weeks. After that, all participants will have a 2-week follow-up period to check on safety.

02

Conditions studied

  • Type II Diabetes Mellitus

Keywords

  • Type 2 Diabetes Mellitus
  • HbA1C
  • Percentage change in HbA1C
  • Change in Fasting Plasma Glucose
  • Change in body weight
  • Body weight loss
  • Hypoglycemics episodes
  • Hypoglycemia
  • Continuous Glucose Monitoring
  • Blood glucose
  • Health Survey Short Form-36
  • Diabetes treatment satisfaction questionnaire
  • Columbia-suicide severity rating scale
03

In context

Diabetes Mellitus, Type 2

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

This study's enrollment of 251 is above the median of 80 across 8,350 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Corxel Pharmaceuticals is the lead sponsor of 12 studies on the registry; 2 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

Participants who meet all of the following criteria will be eligible to participate in this study:

  • Adults aged 18 to 75.
  • Diagnosis of type 2 diabetes for at least 6 months.
  • between 7.0% and 10.5%.
  • (BMI) between 23 and 50 kg/m².
  • Body weight stable for the past 3 months before joining.
  • Stable dose of metformin (≥1000 mg/day), with or without SGLT2i, for ≥3 months.
  • Women of (WOCBP): highly effective ≥6 months prior to screening, throughout study, and 90 days post-last dose; negative pregnancy test within 24 hrs of first dose; no intent to donate sperm/ova
  • Agrees to avoid grapefruit/grapefruit products

Exclusion criteria

Exclusion Criteria

Participants who meet any of the following criteria will be excluded from this study:

  • Anticipated initiation or change in concomitant medications (for more than 14 consecutive days) known to affect weight or glucose metabolism (e.g. treatment with orlistat, thyroid hormones, or systemic ).
  • Type 1 diabetes or a history of diabetic ketoacidosis.
  • Use of any GLP-1 receptor agonist within the past 6 months, or any prior exposure to CX11.
  • Use of insulin to control blood sugar within the past 12 months.
  • More than one episode of severe low blood sugar, with awareness of hypoglycemia symptoms.
  • Cardiovascular or cerebrovascular conditions within the past 6 months:

    • Heart attack, coronary angioplasty, or bypass surgery (diagnostic angiography allowed).
    • Valvular heart disease or prior heart valve repair surgery.
    • Unstable angina.
    • (TIA) or stroke.
    • Decompensated heart failure ( Class III or IV).
    • abnormalities indicating significant safety risk, such as supraventricular tachycardia, torsades de pointes, second- or third-degree AV block, myocardial infarction, > 450 ms in males or > 470 ms in females, PR interval > 220 ms.
    • Poorly controlled hypertension at screening: systolic ≥ 180 mmHg or diastolic ≥ 100 mmHg.
  • Pancreatic or gallbladder conditions:

    • Acute or chronic pancreatitis.
    • Symptomatic gallbladder disease (previous cholecystectomy is allowed).
    • Pancreatic injury or risk factors that increase pancreatitis risk.
  • Thyroid conditions:

    • Poorly controlled abnormal thyroid function on a stable dose before screening.
    • abnormal thyroid test results at screening.
    • Personal or first-degree family history of medullary thyroid carcinoma or multiple endocrine neoplasia (MEN) type 2A or 2B.
  • Cancer history:

    • within the past 5 years, regardless of recurrence or . Exceptions: localized basal cell skin cancer, low-risk prostate cancer, cervical carcinoma in situ, or high-grade prostatic intraepithelial neoplasia.
  • Gastrointestinal conditions or treatments that may affect drug absorption:

    • Abnormal gastric emptying (e.g., gastric outlet obstruction).
    • Severe chronic gastrointestinal disease, including active ulcer within 6 months.
    • Crohn's disease, ulcerative colitis, or other inflammatory bowel diseases.
    • Prior gastrointestinal surgery (except polypectomy and appendectomy).
    • Long-term use of drugs that directly affect gastrointestinal motility (e.g., mosapride, cisapride).
  • Liver disease:

    • Active liver disease other than nonalcoholic fatty liver.
    • Chronic active or C.
    • Primary biliary cirrhosis.
  • Eye disease:

    • Uncontrolled or potentially unstable diabetic retinopathy or maculopathy.
  • Abnormal lab results at screening:

    • \< 60 mL/min/1.73 m² (CKD-EPI).
    • or AST > 2.5 × (ULN).
    • Total > 1.5 × ULN (except known Gilbert's syndrome).
    • Serum amylase or lipase > 1.5 × ULN.
    • Fasting triglycerides > 5.7 mmol/L.
    • TSH > 1.5 × ULN or \< 1.0 × LLN.
    • Calcitonin ≥ 20 ng/L.
    • \< 110 g/L (male) or \< 100 g/L (female).
Terms in these criteria, in plain language(18)

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.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

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.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
251 participants (actual)

Study arms

  • Placebo comparator
    Placebo group

    Other: Placebo

  • Experimental
    40 mg group

    Drug: CX11

  • Experimental
    80 mg group

    Drug: CX11

  • Experimental
    120 mg group

    Drug: CX11

  • Experimental
    160 mg group

    Drug: CX11

  • Experimental
    200 mg group

    Drug: CX11

Interventions

  • DrugCX11

    CX11 tablets administered orally once daily (QD)

    Also known as: VCT220

  • OtherPlacebo

    Matching placebo tablets administered orally once daily (QD)

06

What researchers measure

Primary outcomes

  1. Change in Glycosylated hemoglobin, Type A1C (HbA1c) from baseline

    Time frame: At Week 24

Secondary outcomes

  1. Proportion of participants achieving HbA1c < 7.0%

    Time frame: At Week 24

  2. Proportion of participants achieving HbA1c ≤ 6.5%

    Time frame: At Week 24

  3. Change from baseline in Time in Range (TIR) measured by Continuous Glucose Monitoring (CGM)

    Time frame: To Week 24

  4. Change from baseline in fasting plasma glucose (FPG)

    Time frame: To Week 24

  5. Change in body weight from baseline

    Time frame: To Week 24

  6. Percent change in body weight from baseline

    Time frame: To Week 24

  7. Proportion of participants achieving body weight loss ≥ 5%

    Time frame: At Week 24

  8. Proportion of participants achieving body weight loss ≥ 10%

    Time frame: At Week 24

  9. Change in Systolic Blood Pressure (SBP) from baseline

    Time frame: To Week 24

  10. Change in Diastolic Blood Pressure (DBP) from baseline

    Time frame: To Week 24

  11. Number of Level 2 hypoglycemic episodes (glucose <54 mg/dL)

    Time frame: To Week 24

  12. Number of severe hypoglycemic episodes

    Time frame: To Week 24

  13. Number of treatment-emergent adverse events (TEAEs)

    Time frame: Study duration, approximately 26 weeks

  14. Number of AEs of special interest (AESIs)

    Time frame: Study duration, approximately 26 weeks

  15. Plasma drug concentrations at each specified sampling time point

    Time frame: At Weeks 2, 4, 6, 8, 12, 16, 22 and 24

  16. Mean plasma drug concentration at each specified sampling time point

    Time frame: At Weeks 2, 4, 6, 8, 12, 16, 22 and 24

07

Study locations

44 sites
  • Central Research Associates - Flourish - PPDS
    Birmingham, Alabama 35205-1605, United States
  • AES - DRS - Synexus Clinical Research US, Inc. - Birmingham
    Birmingham, Alabama 35211-1320, United States
  • AES - DRS - Optimal Research Alabama - Huntsville
    Huntsville, Alabama 35802-2569, United States
  • Core Healthcare Group
    Cerritos, California 90703, United States
  • Ark Clinical Research - Long Beach
    Long Beach, California 90815-2521, United States
  • Flourish Research - Walnut Creek - PPDS
    Walnut Creek, California 94598-3343, United States
  • AES - DRS - Optimal Research Florida - Melbourne
    Melbourne, Florida 32934-8172, United States
  • Tampa General Hospital
    Tampa, Florida 33606-3571, United States
  • Conquest Research LLC - Winter Park
    Winter Park, Florida 32789-1857, United States
  • Privia Medical Group Georgia, LLC - Albany - Javara - PPDS
    Albany, Georgia 31707-0205, United States
  • Javara Inc. - Fayetteville
    Fayetteville, Georgia 30214, United States
  • Privia Medical Group Georgia, LLC - Savannah - Javara - PPDS
    Savannah, Georgia 31406-3928, United States
  • AES - DRS - Synexus Clinical Research US, Inc. - Chicago
    Chicago, Illinois 60602-3960, United States
  • AES - DRS - Synexus Clinical Research US, Inc. - Evansville
    Evansville, Indiana 47714-7513, United States
  • Privia Medical Group, LLC - Kelly's Collaborative Care - Javara - PPDS
    Silver Spring, Maryland 20901-1586, United States
  • Elixia Health - Michigan Kidney Consultants, LLC - Elixia - PPDS
    Pontiac, Michigan 48341, United States
  • AES - DRS - Synexus Clinical Research US, Inc. - Edina - Minneapolis
    Edina, Minnesota 55435-4305, United States
  • Mankato Clinic - East Main Street - Javara - PPDS
    Mankato, Minnesota 56001, United States
  • Sky Integrative Medical Center
    Ridgeland, Mississippi 39157, United States
  • Hassman Research Institute - Berlin - CenExel - PPDS
    Berlin, New Jersey 08009, United States
  • Albuquerque Clinical Trials Inc
    Albuquerque, New Mexico 87102-2619, United States
  • Brooklyn Clinical Research
    Brooklyn, New York 11226, United States
  • M3 Wake Research, Inc - M3 WR
    Raleigh, North Carolina 27612-8106, United States
  • M3 Wake Research - Dallas
    Dallas, Texas 75246, United States
  • University of Texas Southwestern Medical Center
    Dallas, Texas 75390-7202, United States
  • SMS Clinical Research, LLC - 400 W. Kearney St
    Mesquite, Texas 751497, United States
  • AES - DRS - Synexus Clinical Research US, Inc. - San Antonio
    San Antonio, Texas 78229-3272, United States
  • Flourish Research - San Antonio - PPDS
    San Antonio, Texas 78229-3539, United States
  • Privia Medical Group- North Texas - Stephenville - Javara - PPDS
    Stephenville, Texas 76401-1860, United States
  • Conquest Research - Arlington
    Vienna, Virginia 22182, United States
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Poznaniu
    Poznan, Greater Poland Voivodeship 60-702, Poland
  • Centrum Medyczne Pratia Bydgoszcz - PPDS
    Bydgoszcz, Kuyavian-Pomeranian Voivodeship 85 001, Poland
  • Medyczne Centrum Diabetologiczno-Endokrynologiczno-Metaboliczne
    Krakow, Lesser Poland Voivodeship 31-261, Poland
  • FutureMeds - Krakow - PPDS
    Krakow, Lesser Poland Voivodeship 31-501, Poland
  • METABOLICA Sp. z o.o
    Tarnów, Lesser Poland Voivodeship 33-100, Poland
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial we Wroclawiu
    Wroclaw, Lower Silesian Voivodeship 50-381, Poland
  • AES - DRS - Synexus Polska Sp. Z o.o. Oddzial w Lodzi
    Lodz, Lódzkie 90-127, Poland
  • FutureMeds - Lodz - PPDS
    Lodz, Lódzkie 91-363, Poland
  • FutureMeds - Warszawa Centrum - PPDS
    Warsaw, Masovian Voivodeship 00-215, Poland
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Warszawie
    Warsaw, Masovian Voivodeship 02-672, Poland
  • ETG Warszawa - PPDS
    Warsaw, Masovian Voivodeship 02-677, Poland
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Gdansku
    Gdansk, Pomeranian Voivodeship 80-382, Poland
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Gdyni
    Gdynia, Pomeranian Voivodeship 81-537, Poland
  • AES - DRS - Synexus Polska Sp. z o.o. Oddzial w Czestochowie
    Częstochowa, Silesian Voivodeship 42-202, Poland
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Active, not recruiting
changed Nov 10, 2026
Sites
4 sites removed
Show 4 removed
  • Privia Medical Group Georgia, LLC - Thomasville - Javara - PPDS · Thomasville, United States
  • Elixia Health - Springfield - Elixia - PPDS · Springfield, United States
  • Unity Clinical Research · Oklahoma City, United States
  • Monroe Biomedical Research Charleston · North Charleston, United States
Nov 10, 2026
Primary completion
Apr 16, 2027→Apr 8, 2027
Nov 10, 2026
Study completion
Apr 30, 2027→Apr 15, 2027
Nov 10, 2026
Enrollment
240 (estimated)→251 (actual)
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Recruiting→Active, not recruiting
    4 sites removed
    Show 4 removed
    • Privia Medical Group Georgia, LLC - Thomasville - Javara - PPDS · Thomasville, United States
    • Elixia Health - Springfield - Elixia - PPDS · Springfield, United States
    • Unity Clinical Research · Oklahoma City, United States
    • Monroe Biomedical Research Charleston · North Charleston, United States
    Primary completion Apr 16, 2027→Apr 8, 2027
    Study completion Apr 30, 2027→Apr 15, 2027
    Enrollment 240 (estimated)→251 (actual)
    + 2 other changes: verification date and contact details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07340320
Lead sponsor
Corxel Pharmaceuticals
Responsible party
Sponsor
First posted
Jan 14, 2026
Start date
Feb 6, 2026
Primary completion
Apr 8, 2027 (estimated)
Completion
Apr 15, 2027 (estimated)
Last update
Nov 10, 2026

Oversight

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

Not currently enrolling

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drug tested here: CX11

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