Last reviewed · How we verify

NCT01747642

Study to Evaluate Safety and Therapeutic Efficacy of a Combination Therapy of 'Oncoxin', a Nutritional Supplement and Surafenib, a Multikinase Inhibitor in Patients With Hepatocellular Carcinoma

Status unknown Phase 2/Phase 3 Last updated 11 December 2012
What this trial tests

Phase 2/Phase 3 trial testing Oncoxin in Quality of Life in 60 participants. Status unknown.

Timeline
1 December 2012
Primary endpoint
1 December 2013
1 June 2014

Quick facts

Lead sponsorClinical Research Organization, Dhaka, Bangladesh
PhasePhase 2/Phase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 December 2012
Primary completion1 December 2013
Estimated completion1 June 2014
Sites1 location across Bangladesh

Drugs / interventions tested

Conditions studied

Sponsor

Clinical Research Organization, Dhaka, Bangladesh

Who can join

Adults 18 to 70, any sex, with Quality of Life. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Oncoxin in combination with Surafenib is safe and results in improved survival in patients with hepatocellular carcinoma (HCC)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Quality of Life

Currently open trials in the same condition.

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/NCT01747642.

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