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NCT03541148

Evaluation of Oncoxin-Viusid® in Cutaneous Melanoma

Completed Phase 2 Last updated 30 May 2018
What this trial tests

Phase 2 trial testing Oncoxin-Viusid in Cutaneous Melanoma, Stage II in 20 participants. Completed in 13 April 2018.

Timeline
16 September 2014
Primary endpoint
13 April 2016
13 April 2018

Quick facts

Lead sponsorCatalysis SL
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment20
Start date16 September 2014
Primary completion13 April 2016
Estimated completion13 April 2018
Sites1 location across Cuba

Drugs / interventions tested

Conditions studied

Sponsor

Catalysis SL — full company profile →

Who can join

18 and older, any sex, with Cutaneous Melanoma, Stage II or Malignant Cutaneous Melanoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Malignant melanoma, responsible for 75% of deaths from skin cancer. Current therapeutic options have poor response, many adverse events and high costs. For this reason, a study with nutritional supplement Oncoxin-Viusid was carried out. According to previous studies, it has an antitumor, immunomodulatory effect and to potentiate the antiproliferative effect of standard chemotherapeutic agents in different locations and stages of cancer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Oncoxin-Viusid

Trials testing the same drug.

Other recruiting trials for Cutaneous Melanoma, Stage II

Currently open trials in the same condition.

Other Catalysis SL trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03541148.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing