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| ID | Type | Description | Link |
|---|---|---|---|
| Eudract # :2008-001603-30 |
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The aim of this study is to determine possible molecular changes on large scale gene expression profiling after treatment with Metvix photodynamic therapy (PDT) of actinic keratoses (AK) and cancerised field in renal transplant recipients.
In this study, the whole target area defined by the investigator will be treated by Metvix PDT: this means that both lesions and sub-clinical lesions will be exposed to Metvix PDT. Biopsies will be performed in both regions: lesional and peri-lesional ones. This will allow us to compare pre and post treatment molecular changes that occurred in these regions and so to evaluate if Metvix PDT acts on the sub-clinical lesions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Metvix PDT | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Metvix PDT | Procedure | Methyl aminolevulinate cream will be applied for 3 hours on the whole target field. The target field will then be exposed to red light using Aktilite 128 lamp. |
| Measure | Description | Time Frame |
|---|---|---|
| Percent Change From Baseline in Lesion Count at Week 18 | Percent Change in Lesion Counts at Week 18: Week 18 count minus Baseline count divided by Baseline count multiplied by 100. | Baseline and Week 18. |
| Measure | Description | Time Frame |
|---|---|---|
| Global Percent Change From Baseline in AK Lesion Count in the Target Field (Including New and Recurrent Lesions) at Month15 | Baseline and Month15 |
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Inclusion Criteria:
Exclusion Criteria:
At risk in terms of precautions, warnings, and contra-indication referred in the package insert of Metvix®,
AK lesions clinically atypical or suspicious for malignancy on the target field,
Any of the following topical treatments within the specified washout period at Screening:
Systemic retinoids within the last month prior to Screening visit.
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| Name | Affiliation | Role |
|---|---|---|
| John T. Lear, MB,Ch.B,M.D | Manchester Royal Infirmary | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Dermatology of Manchester Royal Infirmary | Manchester | M13 9WL | United Kingdom |
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9 subjects have been enrolled in one site at United Kingdom. First subject included on: March 11th 2010; Last subject out: October 7th 2011
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| ID | Title | Description |
|---|---|---|
| FG000 | Metvix® Photodynamic Therapy (PDT) |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
Only 9 subjects out of 10 planned ones by the protocol have been included
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| ID | Title | Description |
|---|---|---|
| BG000 | Metvix PDT |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Percent Change From Baseline in Lesion Count at Week 18 | Percent Change in Lesion Counts at Week 18: Week 18 count minus Baseline count divided by Baseline count multiplied by 100. | This trial was of exploratory nature, no statistical rationale for sample size exists. Analysis was performed on Intent to treat (ITT) population that consisted of the entire population enrolled and randomized (i.e., assigned a treatment number). Here, "Overall Number of Participants Analyzed" = participants with available data at specified time point. | Posted | Mean | Standard Deviation | percent change | Baseline and Week 18. |
|
|
From Screening visit up to Month 15/early termination visit
Questioning of subjects at each follow up visit
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Metvix® Photodynamic Therapy (PDT) |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Urinary Track Infection | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Anaemia | Blood and lymphatic system disorders | MedDRA (12.0) | Non-systematic Assessment |
No limitation or caveat on this study
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Farzaneh SIDOU Clinical Project Manager | Galderma | 00 33 4 93 95 70 70 | farzaneh.sidou@galderma.com |
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| ID | Term |
|---|---|
| D055623 | Keratosis, Actinic |
| ID | Term |
|---|---|
| D011230 | Precancerous Conditions |
| D009369 | Neoplasms |
| D007642 | Keratosis |
| D012871 | Skin Diseases |
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| Participants |
|
| Age, Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Participants |
|
|
| Secondary | Global Percent Change From Baseline in AK Lesion Count in the Target Field (Including New and Recurrent Lesions) at Month15 | This trial is of exploratory nature, no statistical rationale for sample size exists. This population consists of the entire population enrolled and randomized (i.e., assigned a treatment number). | Posted | Mean | Standard Deviation | Percent change from baseline | Baseline and Month15 |
|
|
|
| 1 |
| 9 |
| 9 |
| 9 |
| Hyperparathyroidism | Endocrine disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Cataract | Eye disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Vomiting | Gastrointestinal disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Application site pain | General disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Influenza Like illiness | General disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Cellulitis | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
|
| Gastroenteritis viral | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
|
| Lower respiratory tract infection viral | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
|
| Upper respiratory tract infection | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
|
| Urinary tract infection | Infections and infestations | MedDRA (12.0) | Non-systematic Assessment |
|
| Gout | Metabolism and nutrition disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Hyperlipidaemia | Metabolism and nutrition disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Basal cell carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (12.0) | Non-systematic Assessment |
|
| Skin papilloma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (12.0) | Non-systematic Assessment |
|
| Migraine | Nervous system disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Erectile dysfuntion | Reproductive system and breast disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Actinic keratosis | Skin and subcutaneous tissue disorders | MedDRA (12.0) | Non-systematic Assessment |
|
| Telangiectasia | Skin and subcutaneous tissue disorders | MedDRA (12.0) | Non-systematic Assessment |
|
Any intent of the investigator to publish or disclose in any way the information requires the sponsor's prior written approval. The investigator shall provide his draft of such publication to sponsor to review and approve at least 2 months prior to the date of intended publication. Sponsor shall have the absolute right to determine whether information may be published by the investigator.
| D017437 |
| Skin and Connective Tissue Diseases |