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Ongoing Trials


 

Thank you for your interest in taking part in our ongoing trials.

 

 

At times Richmond Pharmacology may be involved in a number of different clinical trials involving healthy volunteers, patients and other specialised volunteer panels.

 


Healthy males and females aged 18-40 wanted for new trial


Clinical trial starting 23rd August! Get £1,030 for your time!
Help us improve current treatments available to patients - volunteer today!
We are carrying out a clinical trial with an investigational drug which is being developed for the treatment of Malaria. The results from this clinical trial will help to work out if this drug can be developed further for testing in patients with Malaria.



Email: volunteer@richmondpharmacology.com

  • Volunteer requirements

You can take part in the study if you meet the following criteria:

  • Males aged 18 to 45 (inclusive)
  • Females aged 18 to 45 of non-childbearing potential. Non-childbearing potential is either (spontaneous) post-menopausal for at least 12 months or pre-menopausal with irreversible surgical sterilization for at least 6 months.
  • You must weigh at least 50kg and have a Body Mass Index (BMI) within the range of 18 and 25 kg/m2(inclusive)
  • You must be healthy with no relevant history of illness or ongoing medical conditions which could interfere with participation in the clinical study
  • You must be a non smoker or a light smoker (5 or less cigarettes a day). Volunteers must be able to abstain from smoking while in the unit.
  • You must consume less than 21 units (males), 14 units (females) of alcohol per week
  • You must not have donated more than 500ml of blood within 90 days
  • You must not test positive for drug or alcohol abuse, pregnancy, hepatitis B/C or HIV.
  • You must not have used any medication or dietary supplements within 7 days of being given the study medication (except paracetamol)
  • You must not have used any herbal supplements within 30 days of being given the study medication
  • Male subjects must agree to use acceptable methods of contraception with their female partner from the time of the first administration of study medication until 100 days following administration of the last dose of study medication

Effective contraceptive methods (for partners) and a full list of medical eligibility requirements will be discussed in detail with the study doctor during screening.

  • Study info

This study will be carried out at our clinical trials unit at Croydon University Hospital in South London and requires an estimated time commitment of up to 6 weeks. Participation will involve one or more screening visits to determine your suitability. If you are included in the study, one in house stay of 4 nights /5 days and 4 out-patient/ follow up appointments. Please refer to the calendar for the proposed study dates.

See below for study dates.

  • Study dates
Cohort 1a- starts 23rd August 2016
Cohort 1b- starts 25th August 2016
  • Study Payment

In recognition of the time involved in taking part in this study, you will receive £1,030 on completion of the study, provided you comply fully with all the study requirements.


  • Speak to our Volunteer Recruitment team

QUOTE 16009

Email: volunteer@richmondpharmacology.com

Call us:  weekdays between 09h00 and 17h00



to speak to a member of our Volunteer Recruitment team o

Ref: MMV_AUG 2016 (email_website_advert_text)

This advertisement has been approved by an ethics committee and any response to this advert will be recorded but you will not be under any obligation to participate in the trial.
The contents of this advert have been approved by an ethics committee. Any response to this advertisement will be recorded.  Your response will not place you under any obligation to participate in this trialYou may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit. 


Register now for more details!


Healthy males and females aged 18-45 wanted for new trial


Get £1,445 for your time!
Help us improve current treatments available to patients - volunteer today!
Study starts 12th September!

Email: volunteer@richmondpharmacology.com

  • Volunteer requirements

You can take part in the study if you meet the following criteria:

  • Male or female volunteers aged 18 and 45 (inclusive)
  • You must be a non smoker or a light smoker (less than 10 cigarettes a day) 
  • You must be healthy with no relevant history of illness or medical conditions and not be on any medication
  • You must consume less than 14 units of alcohol per week 
  • You must not have donated more than 500ml of blood within 90 days 
  • You must not test positive for drug or alcohol abuse, pregnancy, hepatitis B/C or HIV. 
  • You must not have taken any recreational drugs 6 weeks prior to screening
  • Female volunteers of child bearing potential must be willing to use a highly effective method of contraception from 14 days before the administration of the first dose and until 90 days after the last dose of Study Drug and must have a negative pregnancy test. Contraceptive requirements can be discussed in details with the study doctor.
  • Study info

This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. Following a screening assessment, you will be required to stay in our unit for 1 in-house period of 4nights/5days and attend a minimum of 8 outpatient/follow-up appointments.

  • Study dates **NEW DATES**
  • Study Payment

In recognition of the time involved in taking part in this study, you will receive £1,445 on completion of the study, provided you comply fully with all the study requirements. .


  • Speak to our Volunteer Recruitment team


Email:  volunteer@richmondpharmacology.com for details


Call us:  weekdays between 09h00 and 17h00 on +44 (0) 208 664 5200

(choose option 1) to speak to a member of our Volunteer Recruitment team.


Ref: AL7_APRIL 2016 


This advertisement has been approved by an ethics committee and any response to this advert will be recorded but you will not be under any obligation to participate in the trial.
The contents of this advert have been approved by an ethics committee. Any response to this advertisement will be recorded.  Your response will not place you under any obligation to participate in this trialYou may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit. 


Register now for more details!


Healthy males and females aged 18-35 wanted for new trial


Get £1,066 for your time!
Help us improve current treatments available to patients - volunteer today!





Email: volunteer@richmondpharmacology.com

  • Volunteer requirements

You can take part in the study if you meet the following criteria:

  • Male or female volunteers aged between 18 and 35 (inclusive)
  • You must be a non smoker or a light smoker (less than 10 cigarettes a day) 
  • You must be healthy with no relevant history of illness or medical conditions and not be on any medication
  • You must consume less than 14 units of alcohol per week 
  • Have a Body Mass Index (BMI) within the range of 18 and 30 kg/m2 (inclusive)
  • You must not have donated more than 500ml of blood within 90 days 
  • You must not test positive for drug or alcohol abuse, pregnancy, hepatitis B/C or HIV. 
  • You must not have taken any recreational drugs 6 weeks prior to screening
  • Female volunteers of child bearing potential must be willing to use a highly effective method of contraception from 14 days before the administration of the first dose and until 90 days after the last dose of Study Drug and must have a negative pregnancy test. Contraceptive requirements can be discussed in details with the study doctor.
  • Study info

This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. You will be required to attend a total of 6 clinic visits (including screening). One visit will require an in-house. See below for proposed dates..

  • Study dates
Cohort 3 


  • Study Payment

In recognition of the time involved in taking part in this trial, you will receive £1,066 on completion of the study, provided you comply fully with all the study requirements. 

  • Speak to our Volunteer Recruitment team


Email:  volunteer@richmondpharmacology.com for details


Call us:  weekdays between 09h00 and 17h00 on +44 (0) 208 664 5200

(choose option 1) to speak to a member of our Volunteer Recruitment team.


Ref: ALN-HBV0-001_DECEMBER 2016 

This advertisement has been approved by an ethics committee and any response to this advert will be recorded but you will not be under any obligation to participate in the trial.
The contents of this advert have been approved by an ethics committee. Any response to this advertisement will be recorded.  Your response will not place you under any obligation to participate in this trialYou may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit. 


Register now for more details!


Healthy post-menopausal females aged 50-65 wanted for new trial


Get £2,282* for your time!
Help us improve current treatments available to patients - volunteer today!
Trial starts Monday 5th or Tuesday 6th September




Email: volunteer@richmondpharmacology.com

  • Volunteer requirements

You can take part in the study if you meet the following criteria:

  • Female volunteers aged between 50 and 65 (inclusive)
  • You must have been menopausal (i.e. no menstrual cycles) for at least 12 months, without an alternative medical cause.
  • You are not taking hormone replacement therapy (HRT). This ‘wash-out period’ from previous HRT is at least 4 weeks (for oral, transdermal or vaginal therapy) or 6 months (for sex hormone depot injections).
  • You must be a non-smoker or smoke less than or equal to five cigarettes (or use an equivalent amount of tobacco) per day and be willing not to smoke whilst resident in the clinical unit.
  • You must weigh over (or equal to) 50kg and have a Body Mass Index (BMI) within the range of 18 and 32 kg/m2(inclusive)
  • You must be healthy with no significant illness or medical conditions and not be taking any regular medication
  • You must not test positive for drug or alcohol abuse (classed as a regular weekly intake of over 14 units), hepatitis B/C or HIV
  • You must not have donated blood within 90 days
  • Study info

This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. You will be required to attend a screening visit(s) within 21 days of the study start. You will be required to stay in-house for 2 treatment periods. The first treatment period is 28 days long each, the second is 15 days. Each treatment period starts with an inpatient stay of three nights. You will be required to return to the unit for 4 outpatient visits on days 4, 5, 6 and 7 after each dose is given. You will also be required to attend a final follow-up visit 14 days after the dose in period 2..

See below for study dates.

  • Study dates

Screening NOW

1st dates
Admission 1:  Monday 5th September- Dismissal: Thursday 8th September
Out-patient visits:  Friday 9th September, Saturday 10th September, Sunday 11th September, Monday 12th September 
Admission 2: Monday 3rd October- Dismissal: Thursday 6th October 
Out-patient visits: Friday 7th October, Saturday 8th October , Sunday 9th October , Monday 10th October 
Follow up appointment: Tuesday 18th October 

2nd dates 

Admission 1: Tuesday 6th September- Dismissal: Friday 9th September 

Out-patient visits: Saturday 10th September, Sunday 11th September,  Monday 12th September

Admission 2: Tuesday 4th October- Dismissal: Friday 7th October  

Out-patient visits: Saturday 8th October, Sunday 9th October, Monday 10th October, Tuesday 11th October 

Follow up appointment: Wednesday 19th October


  • Study Payment

In recognition of the time involved in taking part in this trial, volunteers will receive £2,282*. This amount is based on the anticipated study plan and will be adjusted pro-rata (i.e. same amount of money paid per unit of time). You must comply fully with all the study requirements. 


  • Speak to our Volunteer Recruitment team

QUOTE 16008

Email: volunteer@richmondpharmacology.com

Call us:  weekdays between 09h00 and 17h00



to speak to a member of our Volunteer Recruitment team o

Ref: OBE0221_MAY 2016 (email_website_advert text)

This advertisement has been approved by an ethics committee and any response to this advert will be recorded but you will not be under any obligation to participate in the trial.
The contents of this advert have been approved by an ethics committee. Any response to this advertisement will be recorded.  Your response will not place you under any obligation to participate in this trialYou may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit. 


Register now for more details!


Paid clinical trial for healthy volunteers aged 25-55- volunteers today!


Clinical trial starting 26th October! Get £5,795 for your time!
Help us improve current treatments available to patients - volunteer today!
We are carrying out a clinical trial with an investigational drug that is being developed for the treatment of diseases related to the immune system. This drug has already been safely administered in single and multiple doses in previous trials. The purpose of this trial is to determine the most effective administration method for this drug.



Email: volunteer@richmondpharmacology.com

  • Volunteer requirements

We are looking for volunteers who fit the following criteria:

  • Healthy male and female subjects aged 25-55 (inclusive, at the time of dosing)
  • You must have a Body Mass Index (BMI) within the range 18 and 29.9 kg/m2 (inclusive) and weigh between 50 and 100 kg (inclusive)
  • You must be a non-smoker or a light smoker (less than 10 cigarettes a day)
  • You must not test positive for drug or alcohol abuse, pregnancy, hepatitis B/C or HIV
  • You must be healthy with no underlying medical conditions that may either interfere with participation in the clinical study, and/or put you at any significant risk
  • You must not have donated plasma within 7 days prior to dosing or donated/lost more than 500 mL of blood within 56 days prior to dosing.
  • You must not consume more than 14 units of alcohol per week on a regular basis or have a history of significant alcohol abuse within 1 year prior to the screening visit
  • Female subjects of childbearing potential, if heterosexually active, must use highly effective or acceptable contraception as defined below, starting at screening and continuing until at least 6 months after study drug administration. Antibiotic prophylaxis is required during this study, which can compromise the efficacy of hormonal contraception. Therefore, it is recommended that subjects using hormonal contraception also use barrier contraception (eg, condom or diaphragm with spermicide) for the duration of antibiotic prophylaxis.
  • Male subjects, if heterosexually active and with a female spouse or partner of childbearing potential or a pregnant or breastfeeding spouse or partner, must agree to use barrier contraception (male condom) for the treatment period and for at least 6 months after study drug administration.
Effective contraceptive methods (for partners) and a full list of medical eligibility requirements will be discussed in detail with the study doctor during screening.

  • Study info

This study will be conducted at our clinical trials unit at Croydon University Hospital in South London and will involve healthy volunteers. The study involves;

1 screening appointment (1 day)
2 vaccination appointments (1 day for each) 2-3 hours required per vaccination
• An in-house stay of 6 days/5 nights
12 out-patient appointments
1 follow-up visit
Please refer to the calendar below for dates:


  • Study Payment

In recognition of the time involved in taking part in this study, you will receive £5,795

This amount will be paid in stages provided you comply fully with all the study requirements. This amount is based on the anticipated study plan. If you are required to attend extra visits you will receive £80 for a day visit or £100 for an overnight visit plus a contribution towards your travel expense of £20.


  • Get in touch

Call our team for more information: +44 (0) 20 8664 5200 (opt 1)
We are open weekdays 9am-5pm
or email us: volunteer@richmondpharmacology.com

Ref: AL4-JUNE 2016 (email_website_advert text)

This advertisement has been approved by an ethics committee and any response to this advert will be recorded but you will not be under any obligation to participate in the trial.
The contents of this advert have been approved by an ethics committee. Any response to this advertisement will be recorded.  Your response will not place you under any obligation to participate in this trialYou may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit. 


Register now for more details!

 

Healthy Volunteer Trials

 

Please choose from the list below the trial you are interested in:

 

 

 

Other Trials

 

Please choose from the list below the trial you are interested in:

 



 

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