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Study details
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Decitabine and Selinexor in Combination to Reverse Drug Resistance With Standard Chemotherapy in Ovarian Cancer

Loyola University
NCT IDNCT05983276ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

40

Study length

about 7.8 years

Ages

18+

Locations

1 site in IL

About this study

This trial is testing a new treatment with four drugs (decitabine, selinexor, carboplatin, and paclitaxel) for ovarian cancer patients whose cancer has returned. The goal is to learn about the side effects and effectiveness of this combination therapy.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Carboplatin
  • 2.Take Decitabine
  • 3.Take Paclitaxel
  • +1 more
PhasePhase 2
DrugCarboplatin
Primary goal40 participants evaluated for safety with treatment-related adverse events and grading using CTCAE 4.3

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

carboplatin, decitabine, paclitaxel (Taxane chemotherapy; stabilizes microtubules), selinexor

Drug routes

injection, intravenous, oral (Oral Tablet)

Endpoints

Primary: 40 participants evaluated for safety with treatment-related adverse events and grading using CTCAE 4.3.

Secondary: 40 participants evaluated for tolerability with treatment-related adverse events and grading using CTCAE 4.3., 40 participants evaluated to determine the clinical efficacy of this novel regimen in both platinum sensitive and resistant recurrent disease as measured by response rates. Response rates (partial response [PR] and complete response [CR])

Body systems

Oncology