Clinical trial · Interventional
Safety and Tolerability Study of the Monoclonal Antibody CT-011 in Patients With Hepatocellular Carcinoma
Phase I/II Safety and Tolerability Study of the Monoclonal Antibody CT-011 in Patients With Hepatocellular Carcinoma
NCT00966251CI-TRIAL-00008313terminatedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The study was stopped because of slow accrual
Summary
Brief summary (as posted)
The objective of this pilot study is to evaluate the safety, tolerability and activity of the monoclonal antibody CT-011 administered intravenously to patients with Primary Hepatocellular Carcinoma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Primary Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CT-011 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CT-011
- interventionNames
- Drug: CT-011
Primary outcomes (1)
- measure
- To assess the safety and tolerability of CT-011 in patients with Primary Hepatocellular Carcinoma
- timeFrame
- 12 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Subjects aged 18 years and above, both genders. 2. Histologically or cytologically confirmed Primary Hepatocellular Carcinoma (HCC) 3. No fibrolamellar subtype HCC 4. Not eligible for any other systemic anti-neoplastic treatment approved for HCC 5. Not eligible for Transarterial chemoembolization (TACE ). 6. No more than 1 prior systemic therapy. Previous TACE or Radiofrequency ablation (RFA) that were used for HCC, are permitted. 7. Not a candidate for curative surgical resection or liver transplantation 8. Measurable disease defined by the identification at least 1 measurable lesion by MRI using RECIST criteria. Tumor in area of TACE or RFA must be enlarging post-procedure to be considered measurable disease. 9. Alpha-fetoprotein (AFP) greater than the upper limit of normal (ULN) 10. Child's Pugh classification A 11. ECOG performance status 0-1 Exclusion Criteria: 1. Patients progressing to liver failure. 2. No core biopsy within the past 7 days 3. Patients who are eligible for Transarterial Chemoembolization (TACE) 4. Patients on concurrent anti-neoplastic therapy (including interferon) 5. Patients who have received any systemic anti-neoplastic therapy not approved for the treatment of HCC. 6. Patients on concurrent steroids, other than those allowed for routine antiemetics, or inhaled steroids 7. Presence of metastasis.
References
Publications (0)
Data not yet available
No reference posted for this study.