Clinical trial · Interventional
PTX-200 and Carboplatin in Ovarian Cancer
A Phase IA/IB Trial of PTX-200 and Carboplatin in Patients With Platinum-Resistant Recurrent Ovarian Cancer
NCT01690468CI-TRIAL-00047308terminatedPhase 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): Enrollment stopped prior to Phase 1b, change in strategic focus
Summary
Brief summary (as posted)
The main purpose of this study is to determine if Triciribine (TCN) and carboplatin are safe and tolerable when given together, and to determine if this combination of drugs can help people with recurrent ovarian cancer.
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 |
|---|---|---|---|
| Ovarian Cancer | Malignant Ovarian Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Carboplatin | Drug | Carboplatin | ALIAS |
| Triciribine | Drug | Triciribine | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Triciribine & Carboplatin
- description
- Phase I/II: 25mg/m\^2 Triciribine and Carboplatin AUC 4. Triciribine escalated to 30, 35, 45mg/m\^2 if toxicities are not encountered. Phase II: Recommended phase II dose of triciribine and carboplatin.
- interventionNames
- Drug: Triciribine
- Drug: Carboplatin
Primary outcomes (1)
- measure
- Maximum Tolerated Dose (MTD)
- timeFrame
- 6 months
- description
- To determine the maximum tolerated dose of TCN-PM when combined with carboplatin in a Phase I clinical trial of biomarker-selected women with platinum-resistant, recurrent or persistent epithelial ovarian, fallopian tube and primary peritoneal cancer (OVCA).
Secondary outcomes (3)
- measure
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * At least 18 years of age * Histologically confirmed, measurable or non-measurable, recurrent or persistent, platinum-resistant epithelial ovarian, fallopian tube or primary peritoneal carcinoma. By standard Gynecologic Oncology Group (GOG) criteria, platinum-resistant disease is defined by a disease-free interval of less than 6 months following treatment with a platinum-based regimen, or the progression of disease during platinum-based therapy. * At least one prior regimen of chemotherapy, with no maximum number of chemotherapy cycles * A serum creatinine ≤ 1.5 mg% obtained ≤ 2 weeks prior to entry * Adequate hematologic reserve obtained ≤ 2 weeks prior to entry: leukocytes ≥ 3,000 mm\^3; absolute neutrophil count ≥ 1500 mm\^3; platelets ≥ 100,000 mm\^3 * Adequate hepatocellular function: aspartate aminotransferase (AST) and alanine transaminase (ALT) ≤ 3x upper limit of normal within institutional limits; bilirubin ≤ 1.5 mg/dl * Gynecologic Oncology Group (GOG) Performance Status of 0, 1, or 2 * Life expectancy of at least 90 days * The patient should be off chemotherapy, biologic therapy and radiation for 28 days. * Neuropathy (sensory and motor) less than or equal to grade 1 per Common Toxicity Criteria (CTC) version 4 Exclusion Criteria: * Prior TCN-PM therapy * History of allergic reactions attributed to compounds of similar chemical or biologic composition to TCN-PM * Patients must be disease-free of prior invasive malignancies for \>2 years with the exception of basal cell or squamous cell carcinoma of the skin. * Inability to give informed consent * Pregnancy * Corrected QT interval (QTc) prolongation \> 450 milliseconds (msec)
References
Publications (0)
Data not yet available
No reference posted for this study.