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Ticagrelor

Phase 2

Coronary Artery Disease | Small molecule | Cardiovascular |Bristol-Myers Squibb Company|Last Updated: Dec 5, 2023

Success Probability

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Market & Valuation

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Trial Design

CONTROLLED
Total Trials1
Total Enrollment58

FDA Designations

No designations recorded

Clinical trial landscape

Ticagrelor · 1 trial · 2 indications

Phase 2 1
NCT05093790A Study to Evaluate BMS-986141 Added on to Aspirin or Ticagrelor or the Combination, on Thrombus Formation in a Thrombosis Chamber Model in Participants With Stable Coronary Artery Disease and Healthy ParticipantsCoronary Artery Disease
COMPLETED58 Analytics
PHASE2COMPLETED
A Study to Evaluate BMS-986141 Added on to Aspirin or Ticagrelor or the Combination, on Thrombus Formation in a Thrombosis Chamber Model in Participants With Stable Coronary Artery Disease and Healthy Participants
Coronary Artery DiseaseUnlock trial analytics

Study Endpoints

Primary Endpoints

Percent Change From Baseline in Thrombus Area
Baseline, Day 1 hour 2, Day 2 hour 24

The change from baseline in thrombus area post-treatment with BMS-986141 versus pretreatment. Baseline is defined as the last non-missing result (including repeated and unscheduled assessments) with a collection date-time less than the datetime of study medication.

Secondary Endpoints

Number of Participants Experiencing Abnormal Vital Signs
Vital signs will be collected at check-in and prior to and after each chamber assessment on Days 1 and 2
Number of Participants Experiencing Abnormal Electrocardiogram (ECG) Values
Electrocardiograms were collected at check-in, and 2 and 24 hours after dosing
Number of Participants Experiencing Clinical Lab Abnormalities
From baseline up to 24 hours post dose
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Treatment Arm 1: Ticagrelor + BMS-986141EXPERIMENTAL -
Treatment Arm 2: Aspirin + BMS-986141EXPERIMENTAL -
Treatment Arm 3: Ticagrelor + Aspirin + BMS-986141EXPERIMENTAL -
Treatment Arm 4: BMS-986141EXPERIMENTAL -

Interventions

NameTypeDescription
TicagrelorDRUGSpecified dose on specified days
BMS-986141DRUGSpecified dose on specified days
AspirinDRUGSpecified dose on specified days
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Eligibility Criteria

Age Range18 Years to 75 Years
SexALL
Healthy VolunteersYes
Study Sites1

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit: www.BMSStudyConnect.com Inclusion Criteria: * Male or female between 18 to 75 years of age, inclusive, and body mass index (weight kg/m2) between 18 and 35 kg/m2 (inclusive), and body weight 50 kg and 1...

Countries:United Kingdom
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Frequently asked questions about Ticagrelor

What is Ticagrelor used for in Coronary Artery Disease?

Ticagrelor is a small molecule being studied for use in Coronary Artery Disease. It is being evaluated in a Phase 2 clinical trial that also includes healthy participants, to assess its effect on thrombus formation when added to aspirin or other antiplatelet therapy. The drug is investigational and not yet approved.

Who makes Ticagrelor?

Ticagrelor is being developed by Bristol-Myers Squibb Company, which trades under the ticker BMY. The company is conducting clinical research on the drug for Coronary Artery Disease, with the most recent trial completed in the United Kingdom.

What phase is Ticagrelor in?

Ticagrelor is in Phase 2 clinical development. The most recent trial, NCT05093790, has been completed. The drug is investigational and has not been approved for any use, so it remains in clinical development for Coronary Artery Disease.

What clinical trials is Ticagrelor in?

Ticagrelor has one completed Phase 2 trial, NCT05093790, which evaluated the drug added on to aspirin or ticagrelor or the combination on thrombus formation in a thrombosis chamber model. The trial enrolled 58 participants with stable Coronary Artery Disease and healthy participants in the United Kingdom.

What does Ticagrelor target?

Ticagrelor is a small molecule that targets the P2Y12 receptor, a key player in platelet activation and thrombus formation. By inhibiting this receptor, the drug aims to reduce blood clot formation, which is relevant in Coronary Artery Disease. This mechanism is being studied in the Phase 2 trial.