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CT-868

Phase 2

Obesity | Small molecule | Metabolic |Roche Holding AG|Last Updated: Feb 5, 2026

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment103

FDA Designations

No designations recorded

Clinical trial landscape

CT-868 · 1 trial · 3 indications

Phase 2 1
NCT05110846A Study of CT-868 in Overweight and Obese Participants With Type 2 Diabetes MellitusObesity
COMPLETED103 Analytics
PHASE2COMPLETED
A Study of CT-868 in Overweight and Obese Participants With Type 2 Diabetes Mellitus
ObesityUnlock trial analytics

Study Endpoints

Primary Endpoints

Change from Baseline in Glycated Hemoglobin A1c (HbA1c) at Week 26
Baseline and Week 26

Secondary Endpoints

Change from Baseline in HbA1c at Week 12
Baseline and Week 12
Percentage of Participants Achieving HbA1c <5.7% at Weeks 12 and 26
Baseline and Weeks 12 and 26
Percentage of Participants Achieving HbA1c ≤6.5% at Weeks 12 and 26
Baseline and Weeks 12 and 26
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
PlaceboPLACEBO_COMPARATORParticipants in the placebo arm received volume- and regimen-matched placebo.
CT-868 1.75 mgEXPERIMENTALParticipants in the CT-868 1.75 mg arm received 1.0 mg/day for 2 weeks followed by 1.75 mg/day for the remaining treatment period.
CT-868 4.0 mgEXPERIMENTALParticipants in the CT-868 4.0 mg arm escalated through 1.0 mg/day for 2 weeks, 1.75 mg/day for 2 weeks, 2.5 mg/day for 4 weeks, 3.25 mg/day for 4 weeks, to 4.0 mg/day for the remaining 14 weeks.

Interventions

NameTypeDescription
PlaceboDRUGParticipants self-injected once-daily subcutaneous volume- and regimen-matched placebo for 26 weeks.
CT-868DRUGParticipants self-injected once-daily subcutaneous CT-868 for 26 weeks according to the randomized dose and regimen.
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Eligibility Criteria

Age Range18 Years to 75 Years
SexALL
Healthy VolunteersNo
Study Sites5

Inclusion Criteria: * Males or Females with T2DM * BMI of ≥27 kg/m2, inclusive * 18-75 years old, inclusive * Stable body weight for 3 months Exclusion Criteria: * Significant medical history * Uncontrolled diabetes * History of malignancy

Countries:Mexico
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Frequently asked questions about CT-868

What is CT-868 used for?

CT-868 is an investigational small molecule being developed for obesity. It was studied in overweight and obese participants with type 2 diabetes mellitus. The drug is in Phase 2 clinical development and is not yet approved by regulatory authorities.

Who makes CT-868?

CT-868 is being developed by Roche Holding AG, which trades under the ticker RHHBY. The company is conducting clinical trials to evaluate the drug's safety and efficacy in metabolic conditions such as obesity.

What phase is CT-868 in?

CT-868 is in Phase 2 clinical development. A Phase 2 trial has been completed, and the drug remains investigational. It has not been approved by the FDA or any other regulatory agency for the treatment of obesity.

What clinical trials is CT-868 in?

CT-868 has one completed clinical trial, identified as NCT05110846. This Phase 2 study enrolled 103 participants and evaluated the drug in overweight and obese individuals with type 2 diabetes mellitus. The trial was randomized, double-blind, and placebo-controlled.

Is CT-868 the same as any other drug?

CT-868 is a distinct investigational small molecule developed by Roche. No alternative names for CT-868 have been identified in the available clinical trial information. It is being studied specifically for its potential role in treating obesity.