Safety and Efficacy of RN1001(Avotermin) in Healthy Male Subjects
This study has been completed.
Sponsor:
Renovo
Information provided by:
Renovo
ClinicalTrials.gov Identifier:
NCT00847925
First received: February 17, 2009
Last updated: February 18, 2009
Last verified: February 2009
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Purpose
A double blind, Placebo (Vehicle) and Standard Care controlled, randomised study to investigate the clinical safety and toleration (including systemic pharmacokinetics), wound healing and antiscarring potential of two applications of intradermal RN1001 in healthy male subjects
| Condition | Intervention | Phase |
|---|---|---|
|
Cicatrix |
Drug: Avotermin (RN1001) |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Basic Science |
| Official Title: | A Double Blind, Placebo and Standard Care Controlled, Randomised Study to Investigate the Clinical Safety and Toleration, Wound Healing and Antiscarring Potential of Two Applications of Intradermal RN1001 (Avotermin) in Healthy Male Subjects |
Resource links provided by NLM:
Further study details as provided by Renovo:
Primary Outcome Measures:
- Scar severity [ Time Frame: 12 Months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Treatment local and systemic tolerance [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
| Enrollment: | 103 |
| Study Start Date: | November 2001 |
| Study Completion Date: | September 2003 |
| Primary Completion Date: | September 2003 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
A
50ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
B
20ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
C
5ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
D
100ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
E
500ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
F
0.25ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
G
1ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
H
20ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
|
I
50ng Avotermin/100ul
|
Drug: Avotermin (RN1001)
100ul/linear cm of wound. Dosed before surgery and 24h later
|
Detailed Description:
Double blind, randomised, Placebo and Standard Care controlled, single centre study. Each subject served as their own control, i.e. Arm 1 incisions/biopsies randomly received one of two treatments and Arm 2 incisions/biopsies received the same treatments as for Arm 1 but in reverse. The randomisation of the treatment allowed for control of possible positional effects on healing and subsequent scarring. Subjects were initially dosed and wounded (incisions and punch biopsies) on Day 0 and re-dosed on Day 1. On Day 3, Arm 1 incisions and punch biopsies were re-dosed as per Day 0 and excised, and re-dosed again on Day 4. Arm 2 punch biopsies were excised at Day 5 but not re-dosed. Healed incisions/scars on Arm 2 were excised for histological analysis after 12 months and not re-dosed. All subjects, regardless of treatment were treated according to best practices for moist wound healing.
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Healthy, non-Afro-Caribbean, male subjects aged 18-45 years inclusive.
- Weight between 60 and 150kg and a body mass index between 15 - 55 kg/m2.
- Subjects who have a previous history of surgery or minor injury and who have not developed any evidence of hypertrophic or keloid scar formation
Exclusion Criteria:
- Subjects who on direct questioning and physical examination have history or evidence of hypertrophic or keloid scarring.
- Afro-Caribbean subjects are excluded because of the increased susceptibility to hypertrophic and keloid scarring.
- Subjects with tattoos or previous scars in the areas to be biopsied.
- Subjects, who on direct questioning and physical examination, have evidence of any past or present clinically significant disease and particularly coagulation disorders, immuno mediated conditions and skin diseases and allergies, such as eczema.
- Subjects with a history of clinically significant allergies, especially drug hypersensitivity to lignocaine or allergy to the surgical dressings to be used in this study.
- Subjects with any clinically significant abnormality following review of pre study laboratory data and full physical examination.
- Subjects who are taking, or have taken, certain prescribed or investigational drug in the three weeks prior to Day 0 and in particular topical or systemic steroids, and anti-coagulant drugs. Certain drugs are not excluded in this trial. These include OTC analgesics including paracetamol and codeine, vitamin and mineral supplements, inhaled salbutamol, thyroxine replacement therapy, OTC cold remedies.
- Subjects who drink more than 28 units of alcohol per week (1 unit = ½ pint of beer (285mls) or 25ml of spirits or 1 glass of wine).
- Subjects who have current evidence of drug abuse.
- Subjects who are known to have or had serum hepatitis or who are carriers of the hepatitis B surface antigen or hepatitis C antibody. Subjects with previous vaccination against Hepatitis B are not excluded per se.
- Subjects who are known to have or had serum hepatitis or who are carriers of the hepatitis B core antibody and who show less than 10 units per litre of Anti-HBs.
- Subjects who have previously had a positive result to the test for HIV antibodies, or who admit to belonging to a high-risk group.
- In the opinion of the investigator, a subject who is not likely to complete the study for what ever reason.
Contacts and Locations More Information
No publications provided by Renovo
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Mark Cooper, Renovo |
| ClinicalTrials.gov Identifier: | NCT00847925 History of Changes |
| Other Study ID Numbers: | RN1001-309-1002 |
| Study First Received: | February 17, 2009 |
| Last Updated: | February 18, 2009 |
| Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
Additional relevant MeSH terms:
|
Cicatrix Fibrosis Pathologic Processes |
ClinicalTrials.gov processed this record on September 26, 2012
