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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.

 


Are you healthy and aged 18-60?

We are no longer recruiting for this study - please refer to our other trial listings for details on our ongoing studies.

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We are reaching out to healthy non-smoking volunteers for a clinical trial starting 28 April.


  • Who can take part?
You may be suitable to take part if you are a healthy non-smoker aged 18 to 60. If you are a female volunteer you must be of non-childbearing potential i.e. post-menopausal or surgically sterilised.

  • Study summary
This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. You'll first need to attend a screening appointment at our unit to check that you are suitable to take part. If you are included in this study you will need to stay at our unit for two in-patient stays of 2 nights and attend 15 x out-patient visits (lasting up to an hour per visit) including a final follow up.

  • Study commitment

We are no longer recruiting for this study - please refer to our other trial listings for details on ongoing studies.


  • Study payment
In recognition of the time involved in taking part in this study, you will receive £1,950 on completion of the study provided you comply fully with all the study requirements. Travel assistance will be provided for the screening visit and study visits if you are included in the study.
  • Speak to our Volunteer Recruitment team

If you are interested in finding out more Click here to register

Email volunteer@richmondpharmacology.com for details

Or

Call us on +44 (0)20 8664 5200 (choose option 1) and speak to a member of our Volunteer Recruitment Team.

A detailed information sheet is available on request.


  • Recommend a friend
If you don't meet the study criteria but have a friend or family member who may be suitable for this trial, you will compensated £90 for your referral if they go on to complete the study, or this payment can be donated to a charity of your choice. With their consent please send your full name and your friend's or family member's name and contact telephone number to volunteer@richmondpharmacology.com


Ref: AL1_OCT 2014 (email text) | C14048 email text_V2.0_17.10.14

Register now for more details!


Do you have high cholesterol?

We are no longer recruiting for this study - please register and we will keep you posted on similar studies that may arise in future. 

 

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We are carrying out a clinical trial of a potential new treatment for hypercholesterolemia, a condition where there is higher than normal level of ďbad cholesterolĒ (also known as LDL cholesterol or LDL-C) in the blood. 

  • Who can take part?

You may be suitable to take part if you are healthy non-smoker aged 18 to 75, with a higher than normal level of LDL-C cholesterol. You must be on a stable dose of statin medication for more than a month. If you are a female volunteer you must be of non-childbearing potential i.e. post-menopausal or surgically sterilised. 

  • Study summary
This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. You'll first need to attend a screening appointment at our unit to check that you are suitable to take part. If you are included in the study commitment will involve two in-patient stays of 2 nights and 10  out-patient visits including a final follow up visit.

  • Study commitment 

Screening appointments will be held up to 24 April inclusive.

In-patient stay 1


Admission: 28th April

Dismissal: 30th April

Outpatient visits


Visit 1: 1st May

Visit 2: 3rd May

Visit 3: 6th May

Visit 4: 13th May

Visit 5: 20th May

In-patient stay 2


Admission: 26th May

Dismissal: 28th May

Outpatient visits


Visit 1: 3rd June

Visit 2: 10th June

Visit 3: 24th June

Visit 4: 1st July

Visit 5: 8th July


Follow-up visit: 22 July


  • Reimbursement for your time 

In recognition of the time involved in taking part in this study, you will receive £1,720 on completion of the study provided you comply fully with all the study requirements. Travel assistance will be provided for the screening visit and study visits if you are included in the study.

  • Speak to our Volunteer Recruitment team

If you are interested in finding out more Click here to register

Email statin@richmondpharmacology.com for details

Or

Call us on +44 (0)20 8664 5200 (choose option 1) and speak to a member of our Volunteer Recruitment Team.

A detailed information sheet is available on request.


  • Recommend a friend
If you don't meet the study criteria but have a friend or family member who may be suitable for this trial, you will compensated £250 for your referral if they go on to complete the study, or this payment can be donated to a charity of your choice. With their consent please send your full name and your friend's or family member's name and contact telephone number to statin@richmondpharmacology.com


Ref:  ⁞AL1_OCT 2014 (web story) | C14048 web story_V2.0_17.10.14

The contents of this  web page 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 trial.

You 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!


Are you healthy and aged 18-45?

We are carrying out a clinical trial in healthy volunteers to test the safety and tolerability of a potential new treatment for paroxysmal nocturnal hemoglobinuria (PNH), a life-threatening disease that destroys red blood cells.

  • Who can take part?

 

You may be suitable to take part if you are healthy and aged 18 to 45. If you are a smoker you must smoke less than 10 cigarettes or equivalent per day.

  • Study summary

 

This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. Youíll first need to attend three screening appointments at our unit to check that you are suitable to take part, and to be vaccinated against the bacteria causing pneumonia and sepsis before dosing to reduce the risk of infection and you will be given antibiotics. This study is made up of two parts, a Single Ascending Dose (SAD) part involving healthy volunteers (Part A) and a Multiple Dose (MD) part involving healthy volunteers (Part B). Volunteers may only take part in one part of the study .

  • Study commitment 

 

3 x initial screening visits 
1 x in-patient stay of 3 days (2 nights)

8 x out-patient visits

Please ask a member of our team for dates for the next study group. 


  • Study payment
In recognition of the time involved in taking part in this study, you will receive £2,245 on completion of the study provided you comply fully with all the study requirements. Travel assistance will be provided for the screening visit and study visits if you are included in the study.

  • Speak to our Volunteer Recruitment team
If you are interested in finding out more Click here to register

Email volunteer@richmondpharmacology.com for details

Or

Call us on +44 (0)20 8664 5200 (choose option 1) and speak to a member of our Volunteer Recruitment Team.

  • Recommend a friend
If you donít meet the study criteria but have a friend or family member who may be suitable for this trial, you will compensated £90 for your referral if they go on to complete the study, or this payment can be donated to a charity of your choice. 
With their consent please send your full name and your friendís or family member's name and contact telephone number to volunteer@richmondpharmacology.com 

Ref:  AL2_DEC 2014 (web story) | C14050 web story_V1.0_04.12.14

The contents of this web page 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 trial.

You 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!


Are you a healthy male or female aged 18-65?

We are carrying out a clinical trial of a medicated cream being developed for the treatment of skin conditions. You may be suitable to take part if you are a healthy male or female aged 18 to 65 (inclusive), and you are of Caucasian (i.e. European , middle eastern or north African) or Japanese ancestral origin.
  • Study summary
This study will be carried out at our clinical trials unit at Croydon University Hospital in South London. Youíll first need to attend a screening appointment at our unit to check that you are suitable to take part. If you are included in this study you will receive daily applications of the study cream at our unit for 29 days including 4 in-patient stays of 3 days (2nights) and daily out-patient visits to our unit. Youíll also need to attend 3 follow-up visits including a final follow-up visit at the end of the study.
  • Study commitment 
1 x initial screening visit 
4 x in-patient stays of 3 days (2 nights) + daily out-patient visits over 29 days
3 x follow-up visits including a final follow-up

Please ask a member of the team for dates for the next study group.
  • Reimbursement for your time
In recognition of the time involved in taking part in this study, you will receive £1,490 on completion of the study and a discretionary bonus payment of £740 provided you comply fully with all the study requirements. If you are included in the study we will pay for your travel to the site daily or you will have the opportunity to stay at nearby accommodation for the whole study duration (except during the screening phase) which we will arrange for you and pay for.

  • Speak to our Volunteer Recruitment team
If you are interested in finding out more Click here to register

Email volunteer@richmondpharmacology.com for details

Or

Call us on +44 (0)20 8664 5200 (choose option 1) and speak to a member of our Volunteer Recruitment Team.

  • Recommend a friend
If you donít meet the study criteria but have a friend or family member who may be suitable for this trial, you will compensated up to £250 for your referral if they go on to complete the study, or this payment can be donated to a charity of your choice. 

With their consent please send your full name and your friendís or family member's name and contact telephone number to volunteer@richmondpharmacology.com

Ref:  GL1_OCT 2014 (web story) | C14065 web story (non-Japanese)_V2.0_05 12 14

The contents of this web page 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 trial.

You 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!


Do you have difficulty getting or maintaining an erection?

We are carrying out a clinical trial in male volunteers for an investigational gel which is being developed for the treatment of diagnosed or self-diagnosed Erectile Dysfunction (ED). ED, also known as impotence, is the inability to get and maintain a proper erection. The results from this study will help us to plan for future clinical trials to further develop the gel as an approved treatment.

  • Who can take part?
You may be suitable to take part if you are a male aged 18 to 70 inclusive, and self-diagnosed with ED for 3 months or more according to the NIH Consensus Statement (ďthe inability to achieve or maintain penile erection sufficient for satisfactory sexual performance at least once.Ē). To participate in this study you will need to be in a heterosexual relationship for at least 6 months and your female partner must be willing to provide consent to participate in study activities.

  • Study summary
You and your and your female consenting partnerís involvement in this study will last approximately 19 weeks. Youíll first need to complete a pre-screening questionnaire to check that you are suitable to take part, and if you qualify, you will be invited to attend a screening appointment at our clinical trials unit at Croydon University Hospital in South London.

If you would consider yourself to be suitable for this study, Click here to complete the initial pre-screening questionnaire.

  • Study participation
If you are invited to take part in the study, you and your partner will be asked to participate in a 4 week run-in period before the start of the study in order for us to get baseline information for questionnaires. Participation in this study will involve two treatment periods of 4 weeks, during which time you will be given the study gel to apply at home. You will also need to attend 6 outpatient visits (3 of which your female consenting partner will also need to attend) and a final follow-up visit (i.e. there are no in-house periods).
  • Study commitment 
1 x initial screening visit
2 x treatment periods of 4 weeks +/- 1 week including 6 outpatient visits
1x follow-up visit

Please ask a member of the team for details on the study dates.

  • Study payment
In recognition of the time involved in taking part in this study, you will receive £780 on completion of the study provided you comply fully with all the study requirements. Additionally your partner will receive £240 for her time involved in this study.

  • Speak to our Volunteer Recruitment team 

If you are interested in finding out more Click here to register

Email volunteer@richmondpharmacology.com for details

Or

Call us on +44 (0)20 8664 5200 (choose option 1) and speak to a member of our Volunteer Recruitment Team.

A detailed information sheet is available on request.


Or 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.

  • Recommend a friend
If you donít meet the study criteria but have a friend or family member who may be suitable for this trial, you will compensated £250 for your referral if they go on to complete the study, or this payment can be donated to a charity of your choice. 
With their consent please send your full name and your friendís or family member's name and contact telephone number to volunteer@richmondpharmacology.com

Ref: FT1_FEB 2015 (email / online advert / web story text)

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 trial.

You 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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