Melanoma Clinical Trial
Official title:
Phase II Multicenter Randomized Study to Compare Dacarbazine With Melatonin or Metformin Versus Dacarbazine in the First Line Therapy of Disseminated Melanoma
NCT number | NCT02190838 |
Other study ID # | MMM-1 |
Secondary ID | |
Status | Terminated |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | April 2014 |
Est. completion date | December 31, 2018 |
Verified date | September 2019 |
Source | N.N. Petrov National Medical Research Center of Oncology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Treatment of disseminated melanoma is still a difficult issue. Obvious achievements of recent years proves efficacy of immunologic approachees in this field. The ability of melatonin and metformin to decrease metabolic immunosuppression was shown in many experimental studies. Some literature data confirm the possibility of increasing efficacy of melatonin with dacarbazine (DTIC) and metformin with DTIC combinations. We hypothesized that this combinations could be more effective than DTIC monotherapy in terms of response rate and time to progression.
Status | Terminated |
Enrollment | 57 |
Est. completion date | December 31, 2018 |
Est. primary completion date | December 12, 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age >18. - Obtained Inform Consent - Morphologically confirmed disseminated Stage IV melanoma - Eastern Collaborative Oncology Group Performance Status Scale 0 - 2. - Expected survival >3 month Exclusion Criteria: - Evidence of active brain lesions (brain lesions after stereotaxic ray therapy allowed) - Evidence of liver and bone marrow clinically meaningful disfunction - Severe uncontrolled concomitant conditions and diseases - Pregnancy or lactation - Systemic therapy for disseminated melanoma - Second malignancy - Diabetes mellitus requiring drug therapy - Any condition preventing study participation by investigator opinion |
Country | Name | City | State |
---|---|---|---|
Russian Federation | N.N. Petrov Research Institute of Oncology Ambulatory Chemotherapy Department | St. Petersburg | |
Russian Federation | N.N. Petrov Research Institute of Oncology Chemotherapy and Innovative Technologies Department | St. Petersburg | |
Russian Federation | N.N. Petrov Research Institute of Oncology Clinical Diagnostic Department | St.Petersburg |
Lead Sponsor | Collaborator |
---|---|
N.N. Petrov National Medical Research Center of Oncology |
Russian Federation,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Response Rate | Per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. ORR is defined as the proportion of patients with a best overall response of complete response or partial response | 23 months after FPFV | |
Primary | Progression Free Survival | As per RECIST v1.1. progression-free survival (PFS) is the time from date of randomization/start of treatment to the date of event defined as the first documented progression or death due to any cause. | 23 months after FPFV | |
Secondary | Adverse events (AE) incidence | Incidence of AE classified using NCI Common Terminology Criteria for AE v4 | until 30 days after last patient treatment visit | |
Secondary | Metabolic Changes Incidence | Nutritional status will be assessed using Nutritional Risk Index (NRI), Subjective global assessment (SGA), and Body Mass Index (BMI) tools. | 23 months after FPFV | |
Secondary | Immune system assessment | Following tests will be performed at baseline and each response assessment: Lymphocyte subpopulations detection Immunosuppressive factors measurements |
23 months after FPFV |
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