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Capadenoson

Phase 2

Atrial Fibrillation | Small molecule | Cardiovascular |Bayer AG|Trials Updated: Oct 29, 2014

Capadenoson target and mechanism

Molecular targetADORA1
Target classPartial Agonist
ModalitySmall molecule

Also known as Capadenoson (BAY68-4986)

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment28

FDA Designations

No designations recorded

Capadenoson clinical trials

Capadenoson · 1 trial · 1 indication

Phase 2 1
NCT00568945Study to Investigate the Effect of the A1 Agonist Capadenoson on Ventricular HR in Patients With Persistent or Permanent Atrial Fibrillation.Atrial Fibrillation
COMPLETED28 Analytics
PHASE2COMPLETED
Study to Investigate the Effect of the A1 Agonist Capadenoson on Ventricular HR in Patients With Persistent or Permanent Atrial Fibrillation.
Atrial FibrillationUnlock trial analytics

Study Endpoints

Primary Endpoints

The effect of capadenoson (BAY68-4986) on rate control in patients with atrial fibrillation
1 week

Secondary Endpoints

To investigate safety and tolerability of this treatment with capadenoson
2 weeks
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Arm 1EXPERIMENTAL -

Interventions

NameTypeDescription
Capadenoson (BAY68-4986)DRUG4 mg BAY68-4986 for five days
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Eligibility Criteria

Age Range18 Years to 75 Years
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Male and/or female (without childbearing potential) white patients * History of persistent or permanent atrial fibrillation * 18 to 75 years of age Exclusion Criteria: * Patients with high-risk cardiovascular diseases * Stroke or myocardial infarction * Relevant pathological...

Countries:Germany
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Competitive Landscape -Atrial Fibrillation 159 trials

Frequently asked questions about Capadenoson

What is Capadenoson used for?

Capadenoson is an investigational small molecule being studied for atrial fibrillation, a common heart rhythm disorder. It was evaluated in a Phase 2 study of patients with persistent or permanent atrial fibrillation, where the objective was to investigate its effect on ventricular heart rate. It is not an approved therapy.

What does Capadenoson target?

Capadenoson targets ADORA1, the adenosine A1 receptor, and acts as a partial agonist at that receptor. This receptor is involved in regulating heart rate and electrical conduction in the heart, which is the basis for studying the drug in atrial fibrillation.

Who is developing Capadenoson?

Capadenoson is developed by Bayer AG, which trades on the OTC market under the ticker BAYRY. Bayer sponsored the clinical research conducted on the compound.

What phase is Capadenoson in?

Capadenoson is in Phase 2 development. It is an investigational drug and has not been approved by the FDA for any indication. The completed Phase 2 trial enrolled 28 patients with atrial fibrillation in Germany.

What clinical trials is Capadenoson in?

Capadenoson has been studied in one clinical trial, NCT00568945, titled a study to investigate the effect of the A1 agonist Capadenoson on ventricular heart rate in patients with persistent or permanent atrial fibrillation. That Phase 2 trial is completed and enrolled 28 patients in Germany.

Is Capadenoson the same as BAY68-4986?

Yes. Capadenoson is also known as BAY68-4986, which is Bayer's internal compound designation for the same investigational drug. Both names refer to the same adenosine A1 receptor partial agonist studied in atrial fibrillation.