PRA-177021 (part C) Parkinson’s disease € 775,-

Full

Description

Study of an investigational compound that is being developed for the treatment of Parkinson’s disease

Requested participants

  • M/F, healthy, 60 - 75 years old
  • Non-smokers only

Duration and visits

  • 6 days stay

Learn more about this research?

Research details

Particulars

  • Your Body Mass Index (BMI) is between 18.5 and 35 kg/m2 and your body weight is at least 50kg. The BMI shows the relation between body weight in kilograms and height in meters. 
  • Part C2 only: You are willing to undergo 2 lumbar punctures. During these punctures cerebrospinal fluid will be collected via a lumbar puncture. A fine needle will be inserted at the space between two vertebrae in the lower back.
  • To determine if you are suitable to participate in this study, you will undergo a medical screening visit.
  • You are willing to perform a pulmonary function test as part of the screening, if you are still eligible after the first screening visit. The pulmonary function test will be performed in a second screening visit, so the screening for this study contains 2 screening visits.
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Compensation

You will receive a gross compensation of €775,- for participation in one of the above mentioned groups for Part C1

You will receive a gross compensation of €2624,- for participation in one of the above mentioned groups for Part C2.  

Travelling expenses will be reimbursed based on the distance traveled (€0.19 net per kilometer) with a minimum of € 12,- and a maximum of € 160,- (840 kilometers) per return, regardless of the mode of transportation.

Period of stay and research

For Part C1, the study, consists of 1 period in which you will stay in our research facility in Groningen (location Martini) for 6 days (5 nights).

For Part C2, the study, consists of 1 period in which you will stay in our research facility in Groningen (location Martini) for 15 days (14 nights), followed by two short visits.

Please note: You have to be available for all dates for the group of choice to be able to participate in this study. These are the currently planned dates; however, these may be subject to change.

Do you need more information?

Please call PRA Health Sciences on business days (Monday until Thursday between 08:30 and 20:00 and on Friday between 08:30 and 17:00) on +31 (0)50 8505 798 or send an e-mail to info@prahs.nl. When calling or sending an e-mail, please refer to the indicated study code (PRA-177021). 

Information sheet PRA-177021 (part C)

Type of study

Part C:

This study will be performed in 90 healthy male and female, young and elderly volunteers. The study will be performed in 4 parts, Part A, Part B, Part C1 and Part C2. The remainder of this document concerns Part C only. Part C1 will be performed in approximately 8 elderly volunteers and C2 in approximately 10 elderly volunteers.

The purpose of this study is to investigate how safe the new compound is when it is administered to healthy subjects. The new compound has not been administered to humans before. It has been previously tested in the laboratory and on animals. The new compound will be studied at different strengths. A compound with a similar activity has been tested in humans before.

It will also be investigated how quickly and to what extent the new compound is absorbed and eliminated from the body (this is called pharmacokinetics). In addition, the effect of the new compound on a specific protein will be investigated (this is called pharmacodynamics).

The effects of the new compound will be compared to the effects of a placebo. A placebo is a medicine without any active ingredient. It is a ‘fake’ medicine.

The study will only take place after it has been approved by the Independent Ethics Committee.

Setup and duration of the study

Part C:

To determine if you are suitable to participate in this study, you will undergo a medical screening visit at the centre in Groningen (location Martini). If you pass the first screening you will have to return for a pulmonary test, which is also part of the screening.

Following the two screening visits, if you are eligible for participation, the study consist for Part C1 of 1 period during which you will stay in the research center in Groningen location Martini Hospital for 6 days (5 nights). During this period the new compound or placebo will be given once as oral capsules. For Part C2 the study will consist of 1 period during which you will stay in the research center in Groningen location Martini Hospital for 15 days (14 nights), followed by two short visits. During this period the new compound or placebo will be given as oral capsules once daily on 10 consecutive days.

Blood samples and urine will be taken regularly during the study. In addition for Part C2, cerebrospinal fluid will be collected via a lumbar puncture twice. A fine needle will be inserted at the space between two vertebrae in the lower back. The puncture will be performed in a sitting and stooped position, under local anesthesia and will be performed by a specialist (anesthesiologist). When enough cerebrospinal fluid has been collected (maximum of 6 milliliter), the needle will be removed. After the procedure you will be transferred in a wheelchair to your bed. After that you have to lie down on your back for another 1.5 - 2 hours, this is to decrease the risk on leakage of cerebrospinal fluid.

During the lumbar puncture and the 1.5 to 2 hours thereafter fluid will be administered using an intravenous infusion.

Risks and medical supervision

Part C:

The new compound may cause side effects. As compound will be administered to man for the first time in this study, side effects of the compound in man have not been reported to date. However, the compound has been studied the laboratory and in rats and monkeys. The most frequently observed side effects in animals were: decrease in blood pressure and heart rate.
You should be aware that the adverse events mentioned above and possibly other, still unknown adverse events, may occur during the study.

For Part C2, cerebrospinal fluid will be collected on 2 occasions. Insertion of the needle for the collection of cerebrospinal fluid may be painful. Removing the needle is painless. Usually no complications occur during a lumbar puncture. Sometimes, during the puncture, a nerve can be hit. Then you will feel an electric pulse or a shooting pain in your leg. This can be painful, but is not harmful. This method has been performed with humans before and was generally well tolerated. A number of complaints and complications related to the procedure are already known from previous studies. The most common side effects are headache (post-lumbar puncture headache), back pain and neck pain, discomfort during the procedure, pain at the location of the spinal catheter, dizziness and fainting.

The risks of above mentioned complaints are limited, but you may suffer from these or other, still unknown, complications. To keep the risks as low as possible, your health will be monitored continuously during the study.

Conditions for participation

Part C:

You are a healthy male or female between 60 and 75 years old. You can only take part in the study if you do not smoke.

Females are only allowed to participate in this study if they are sterilized for at least 6 months (Essure® methods is not allowed for this study) or when they are postmenopausal for at least 12 months (without menstrual periods).

The study will be done under standardized conditions. Use of your own medication, alcohol, regular coffee and tea, cola, power drinks, chocolate (including products made of chocolate), grapefruit (juice) and tobacco products during the study are not allowed. Also before the study there will be restrictions for these products. Use of decaffeinated coffee and (herbal) teas without caffeine is allowed. Before you are allowed to take part in the study, you will be medically screened.

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Group C1

€ 775,-

6 days stay

  • 9 Jul 2018 up to and including 14 Jul 2018

short stay

Inapplicable
Group full

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