Choroidal Melanoma, Diffuse Clinical Trial
Official title:
Development and Validation of a Circulating Tumor DNA Detection Technique in Patients With Metastatic Choroidal Melanoma
| NCT number | NCT01334008 |
| Other study ID # | IC 2010-02 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | April 2011 |
| Est. completion date | May 2012 |
| Verified date | January 2024 |
| Source | Institut Curie |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Circulating tumor DNA detection and quantification in patients with metastatic choroidal melanoma.
| Status | Completed |
| Enrollment | 40 |
| Est. completion date | May 2012 |
| Est. primary completion date | February 2012 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Age > or = 18 years. - Patient with a metastatic choroidal melanoma. - Patient with tumor or metastasis available for GNAQ (Guanine nucleotide blinding protein) status characterization. - Patient able to stand a blood collection. - Signed written informed consent approved by competent authority and ethic committee. Exclusion Criteria: - Patient without social protection/insurance. - Current pregnancy and lactation. - All social, medical, psychological, situations making the study impossible. - Person deprived of liberty. |
| Country | Name | City | State |
|---|---|---|---|
| France | Institut Curie | Paris |
| Lead Sponsor | Collaborator |
|---|---|
| Institut Curie |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Assessment and development of circulating tumor DNA detection techniques | Quantification of circulating tumor DNA in blood samples. Results expressed in number of samples where circulating DNA is present. | 2 years | |
| Secondary | Detection technique comparison (PAP (pyrophosphorolysis activated polymerisation), BEAMing, NGS(next sequencing generation)) in terms of feasibility, robustness, sensitivity and cost. | The methods of detection which will be used such as the BEAMing, the PAP (Pyrophosphorolysis-activated polymerization) and NGS (next sequencing generation)is techniques of a big specificity capable of detecting a mutant copy among 1.104 wild copies for the BEAMing, 2.109 for the PAP and 1.105 for the NGS. The sensibility of these techniques is limited by the quantity of genomic DNA which we can extract from the sample of blood. | 2 years |