Evaluation of Ocoxin®-Viusid® in Advanced Stomach Cancer and Gastric Esophagogastric Junction

PHASE2CompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

October 25, 2018

Primary Completion Date

June 15, 2022

Study Completion Date

February 15, 2023

Conditions
Stomach NeoplasmGastrointestinal NeoplasmsDigestive System NeoplasmEsophageal NeoplasmsHead and Neck NeoplasmsGastrointestinal DiseaseDigestive System DiseaseEsophageal DiseasesStomach DiseasesEsophagogastric Junction Disorder
Interventions
DIETARY_SUPPLEMENT

Ocoxin-Viusid®

Ocoxin-Viusid group (Experimental). Oral solution of Ocoxin-Viusid (vials of 30 ml), at a rate of 60 ml daily (1 vial every 12 hours), administrado preferably administered after breakfast and dinner. The product will dilute in water, milk or juice. The treatment will have a period of 19 weeks, starting 2 weeks before the onco-specific treatment with FOLFOX chemotherapy and will end 3 weeks after the end of the sixth cycle of chemotherapy. QT FOLFOX will be prescribed intravenously every 14 days for 6 cycles as follows: Oxaliplatin (85 mg x m2) on day 1 Folinic acid (200 mg x m2) on day 1 and 2 5 Fluoracil (400 mg x m2, bolus) on day 1 and 2 5 Fluoracil (600 mg x m2, continuous infusion) on day 1 and 2

Trial Locations (1)

10400

National Institute of Oncology and Radiobiology (INOR), Havana

All Listed Sponsors
lead

Catalysis SL

INDUSTRY

NCT03549494 - Evaluation of Ocoxin®-Viusid® in Advanced Stomach Cancer and Gastric Esophagogastric Junction | Biotech Hunter | Biotech Hunter