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NCT00659178

Combination Study Of SB-485232 (Interleukin 18) And Doxil For Advanced Stage Epithelial Ovarian Cancer

Completed Phase 1 Last updated 21 July 2017
What this trial tests

Phase 1 trial testing SB-485232 (interleukin 18), pegylated liposomal doxorubicin in Neoplasms, Ovarian in 15 participants. Completed in 18 February 2011.

Timeline
18 June 2008
Primary endpoint
18 February 2011
18 February 2011

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date18 June 2008
Primary completion18 February 2011
Estimated completion18 February 2011
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

18 and older, female only, with Neoplasms, Ovarian. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to identify a dose of SB-485232 which is safe, tolerable and biologically active when used in combination with pegylated liposomal doxorubicin (Doxil) in patients with epithelial ovarian cancer. This study will use a standard treatment regimen of pegylated liposomal doxorubicin (Doxil) in combination with rising doses of SB-485232. The dose selected from this study will be used in a future studies to evaluate the efficacy of this combination.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. IL-18 attenuates experimental choroidal neovascularization as a potential therapy for wet age-related macular degeneration.
    Doyle SL, Ozaki E, Brennan K, Humphries MM, et al · · 2014 · cited 79× · PMID 24695684 · DOI 10.1126/scitranslmed.3007616
  2. Trial Watch: Immunostimulatory cytokines.
    Vacchelli E, Galluzzi L, Eggermont A, Galon J, et al · · 2012 · cited 70× · PMID 22754768 · DOI 10.4161/onci.20459
  3. Involvement of inflammasomes in tumor microenvironment and tumor therapies.
    Zhang Z, Li X, Wang Y, Wei Y, et al · · 2023 · cited 55× · PMID 36932407 · DOI 10.1186/s13045-023-01407-7
  4. Inflammation in cancer: therapeutic opportunities from new insights.
    Xie Y, Liu F, Wu Y, Zhu Y, et al · · 2025 · cited 53× · PMID 39994787 · DOI 10.1186/s12943-025-02243-8
  5. Immunotherapy in ovarian cancer.
    Mantia-Smaldone GM, Corr B, Chu CS. · · 2012 · cited 44× · PMID 22906947 · DOI 10.4161/hv.20738
  6. Advances in Lipid-Based Nanoparticles for Cancer Chemoimmunotherapy.
    Wang T, Suita Y, Miriyala S, Dean J, et al · · 2021 · cited 33× · PMID 33918635 · DOI 10.3390/pharmaceutics13040520
  7. Targeted Nanocarrier-Based Drug Delivery Strategies for Improving the Therapeutic Efficacy of PARP Inhibitors against Ovarian Cancer.
    Gralewska P, Gajek A, Marczak A, Rogalska A. · · 2024 · cited 21× · PMID 39125873 · DOI 10.3390/ijms25158304
  8. Modulating the tumor immune microenvironment with nanoparticles: A sword for improving the efficiency of ovarian cancer immunotherapy.
    Xu T, Liu Z, Huang L, Jing J, et al · · 2022 · cited 15× · PMID 36532066 · DOI 10.3389/fimmu.2022.1057850

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