Ovarian Carcinoma, Recurrent

2

Review clinical trials related to Ovarian Carcinoma, Recurrent. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Intraperitoneal Cytokine-Induced Memory Like (CIML) Natural Killer (NK) Cells in Recurrent Ovarian Cancer

The goal of this research study is to evaluate the safety and effectiveness of the use of cytokine-induced memory-like (CIML) natural killer (NK) cell therapy in recurrent, high grade ovarian cancer (HGOC). Names of the study therapies involved in this study are: CIML NK (cellular therapy) Interleukin-2 (IL-2)

Participants needed: 18
Trial details
Phase: Phase 1Age: 18-85Biological sex: AllType: InterventionalSponsor: Dana-Farber Cancer InstituteUpdated: Jun 16, 2026Locations: 2
Eligibility criteria

Participants must have histologically or cytologically confirmed recurrent epith... [+17]

Participants who have had anti-tumor chemotherapy or other investigational agent... [+15]

Status: Recruiting

Trastzumab Deruxtecan Versus SOC in Recurrent Ovarian That Progressed on Prior PARP Inhibitor Therapy

Ovarian, fallopian tube, and peritoneal cancers are often diagnosed at an advanced stage, requiring chemotherapy. Recently, the standard treatment, platinum-based chemotherapy plus PARP inhibitors, has extended disease-free survival (PFS). However, most patients eventually develop resistance to PARP inhibitors and become unresponsive to conventional treatments. Therefore, an effective standard treatment for patients who relapse after PARP inhibitor resistance has not yet been established. Meanwhile, HER2 protein expression has been identified in some patients, drawing attention as a new therapeutic target. Trastuzumab deruxtecan (T-DXd), an antibody-drug conjugate (ADC) targeting HER2, has already demonstrated efficacy and safety in other HER2-positive cancers. This study aimed to explore the potential of T-DXd as a new treatment option by evaluating the efficacy and safety of T-DXd in patients with ovarian, fallopian tube, and peritoneal cancer who relapsed after PARP inhibitor treatment and who express HER2. Participants will: * Arm A: T-DXd +/- Bevacizumab, IV, every 3weeks * Arm B: Platinum-based chemotherapy +/- Bevacizumab, IV

Participants needed: 116
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Yonsei UniversityUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

1. Adults ≥18 years of age on the day of signing the Informed Consent Form. Foll... [+8]

Participants with HIV infection are eligible if followings are met: a. CD4+ T-ce... [+11]