Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New daily pill CX11 shows promise for obesity in early trial

NCT ID NCT07011797

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed Phase 2 study tested different doses of CX11 tablets against a placebo in 250 overweight or obese adults. Participants took the pill once daily with meals for 36 weeks, followed by a 2-week safety check. The main goal was to see how much weight people lost and whether the drug was safe and tolerable.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
CX11 (also known as VCT220) tablets
What this could lead to
If successful, this could lead to a new daily pill to help people with obesity lose weight and improve related health issues like high blood pressure or prediabetes.
What could go wrong
This is an early Phase 2 trial with only 250 people, so results may not apply to everyone. The drug may cause side effects or fail to show meaningful weight loss compared to placebo.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

250 people

The number who actually took part.

Started

Jun 2025

Finished

Apr 2026

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria Participants who meet all of the following criteria will be eligible to participate in this study: * Between 18 and 75 years old. Both men and women can participate, but women may make up to 70% of the participants. * BMI of 30 or higher, or a BMI between 27 and 30 with at least one related health condition such as prediabetes, high blood pressure, abnormal cholesterol levels, fatty liver, or sleep apnea due to being overweight. * HbA1c level below 6.5% and fasting blood sugar levels below 126 mg/dL. * Have tried and failed to lose weight through diet and exercise at least once before the study and must have had a stable body weight (less than a 5% change) in the 90 days before the study. * Participants and their partners must not plan to become pregnant or donate sperm/eggs during the study and for 90 days after. They must agree to use effective contraception for at least 6 months prior to screening and continue their chosen contraception method throughout the study. Women who could become pregnant must have a negative pregnancy test 24 hours before the first dose of study drug. * Willing to maintain a stable diet and exercise routine during the study and keep a diary of their activities. * Understand the study procedures, be willing to follow the study rules strictly, and sign a consent form voluntarily. Exclusion Criteria Participants who meet any of the following criteria will be excluded from this study: * Known or suspected hypersensitivity to GLP-1 receptor agonists or similar products. * Took part in another clinical study and received treatment within the last 90 days or within 5 drug elimination half-lives. * Any type of diabetes. * Obesity caused by hormonal or genetic issues such as thyroid problems, Cushing's syndrome, or other specific conditions. * Have had or plan to have obesity treatment surgery or use weight loss devices, with some exceptions if done over a year ago. * Have used certain medications or therapies for weight loss or conditions affecting weight, including GLP-1 receptor agonists and other related drugs, within the last 90 days. * Recent serious heart problems, uncontrolled high blood pressure, or certain ECG abnormalities. * History of pancreatitis, gallbladder disease (except for those treated with cholecystectomy), or evidence of hypothyroidism (except for participants who have normal thyroid function at screening and have been on a stable dose thyroid replacement for at least 90 days and are expected to maintain a stable dose during the study) or hyperthyroidism or thyrotoxicosis. * History of cancer in the last 5 years, except for localized basal or squamous skin cancer, in situ carcinomas of the cervix, or in situ prostate cancer. * Serious gastrointestinal diseases or surgeries that affect drug absorption. * Active liver disease, excluding nonalcoholic fatty liver disease. * Other serious health conditions that could increase study risk or make participation inappropriate, including certain psychiatric disorders. * Recent history of unexplained fainting or family history of long QT syndrome or sudden death. * History of organ transplant or severe autoimmune diseases. * Had major surgery within the last 6 months or plan to have surgery soon. * Significant abnormalities in kidney function, liver enzymes, blood tests, or other specified lab results. * Positive for hepatitis B, hepatitis C, or HIV. * Donated blood, lost a lot of blood, or received a transfusion in the last 90 days. * Exceed weekly alcohol intake limits or have a history of drug abuse (including cannabis, its derivatives, or any cannabis-containing products; except for prescribed drug for medical purpose). * Women who are pregnant or breastfeeding. * Any other disease, condition, or medication that the investigator believes would interfere with the study.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Obesity are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Obesity obesity disorder Overweight Weight Loss

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • 310 Clinical Research - Alliance Clinical - Los Angeles

    Inglewood, California, 90301, United States

  • AES - DRS - Optimal Research Florida - Melbourne

    Melbourne, Florida, 32934-8172, United States

  • AES - DRS - Synexus Clinical Research US, Inc. - Phoenix Central

    Phoenix, Arizona, 85020-4327, United States

  • AES - DRS - Synexus Clinical Research US, Inc. - San Antonio

    San Antonio, Texas, 78229, United States

  • Acclaim Clinical Research - Alliance Clinical - San Diego

    San Diego, California, 92120, United States

  • Angels Clinical Research Institute

    Miami, Florida, 33126, United States

  • Angels Clinical Research Institute - Miami

    Doral, Florida, 33122-1713, United States

  • Epic Clinical Research - Alliance Clinical - Lewisville

    Lewisville, Texas, 75057, United States

  • Flourish Research - San Antonio - PPDS

    San Antonio, Texas, 78229, United States

  • Mankato Clinic - East Main Street - Javara - PPDS

    Mankato, Minnesota, 56001, United States

  • Oceanic Research Group, LLC

    North Miami Beach, Florida, 33169, United States

  • Palm Springs Community Health Center

    Miami Lakes, Florida, 33014-2266, United States

  • Privia Medical Group Georgia, LLC - Savannah - Javara - PPDS

    Savannah, Georgia, 31406-3928, United States

  • Privia Medical Group Georgia, LLC - Thomasville - Javara - PPDS

    Thomasville, Georgia, 31792-6618, United States

  • Velocity Clinical Research - Cincinnati (Springdale) - Ohio - PPDS

    Cincinnati, Ohio, 45246-2316, United States

  • Velocity Clinical Research - Dallas - PPDS

    Dallas, Texas, 75230, United States

  • Velocity Clinical Research - Valparaiso (Buynak Clinical Research) - PPDS

    Valparaiso, Indiana, 46383, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.