Study for patients with stable heart failure of ischemic origin

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

We are carrying out a clinical trial with an investigational drug that is being developed with the intention of treating patients with heart failure of ischemic origin (heart failure characterised by a reduced blood supply to the heart).

The main purpose of the study will be to assess how safe the study drug is and to determine how long the study drug will remain in the body. We may also study how the study drug will affect the body.

The information gathered during this clinical trial may be used to support further drug development, including larger trials in patients with heart failure.

 

In recognition of the time and effort involved in taking part in this study, you will receive £1,692 (£1,027 study payment, £505 bonus and up to £160 for travel expenses) on completion of the study provided you comply fully with all the study requirements.

 

For more information about this study:

  • You may also contact us directly; Azar Alexander-Sefre can be reached via e-mail at a.sefre@richmondpharmacology.com or via phone at +44 (0) 207 042 5800

 

Description

In recognition of the time and effort involved in taking part in this study, you will receive £1,692 (£1,027 study payment, £505 bonus and up to £160 for travel expenses) on completion of the study provided you comply fully with all the study requirements.

Details
Condition Heart Stent, Heart Failure, Heart failure, Stent, Ischemic Heart Failure, Ischemic Heart, Coronary Artery Disease
Clinical Study IdentifierTX227267
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or female volunteers, aged between 30 and 80(inclusive)
You must be diagnosed with stable heart failure of ischaemic origin
You must have a Body Mass Index (BMI) within the range 18.0-28.0 kg/m² (inclusive)
You must have a body weight of less than or equal to 100 kg
You must not test positive for hepatitis B/C, HIV, alcohol or drugs or show any evidence of drug or alcohol abuse (Alcohol abuse is defined as a regular weekly intake of more than 14 units)
You must not have donated or lost blood within 16 weeks prior to first dosing
You must not be pregnant or breastfeeding
Female volunteers of childbearing potential, if heterosexually active, must agree to the use of highly effective contraception starting one complete menstrual cycle prior to the first day of dosing and continuing until the follow-up visit
Male volunteers must be willing to use appropriate contraception for the duration of the study and for at least 3 months after the end of study visit. Female spouses or partners of the male volunteer must be willing to use appropriate contraception starting at least one complete menstrual cycle prior to the first day of dosing and continuing until at least 3 months after the end of study visit
You must agree not to donate sperm or ova (eggs) 3 months after end of study visit
Patients for this study are likely to be on medications including diuretics. Read here for a full overview
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note