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RBD1119

Phase 2

Stable Coronary Artery Disease | Small molecule | Other |Fortrea Holdings Inc.|Trials Updated: Oct 20, 2026

RBD1119 development status

Highest phase Phase 2
Registered trials 2 across 2 sponsors since Jun 2025

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindCONTROLLEDDMC
Total Trials1
Total Enrollment200

FDA Designations

No designations recorded

RBD1119 clinical trials

RBD1119 · 1 trial · 1 indication

Phase 2 1
NCT07884136RBD1119 in Coronary Artery Disease (CAD)Stable Coronary Artery Disease
NOT YET_RECRUITING200 Analytics
PHASE2NOT YET_RECRUITING
RBD1119 in Coronary Artery Disease (CAD)
Stable Coronary Artery DiseaseUnlock trial analytics

Study Endpoints

Primary Endpoints

Primary objective
Week 8

To measure the effect of RBD1119 on blood coagulation factor XI activity.

Primary endpoint
Week 8

Change from baseline in blood coagulation factor XI activity.

Secondary Endpoints

Secondary objective
Up to week 44
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Low-dose groupEXPERIMENTAL -
Medium-dose groupEXPERIMENTAL -
High-dose groupEXPERIMENTAL -

Interventions

NameTypeDescription
RBD1119DRUGRBD1119, active drug
PlaceboDRUGPlacebo
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Eligibility Criteria

Age Range50 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites16

Inclusion Criteria: 1. Willing and able to give written informed consent for participation in the trial. 2. Male or female participants age ≥50 years. For male participants, those who are potent and sexually active with a female partner of childbearing potential must agree to use effective male con...

Countries:PolandSweden
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