NCT07273396Not yet recruitingPhase 1/2
Tolerance, Safety, Efficacy, and Pharmacokinetics of Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) Using Paclitaxel for Platinum-resistant Recurrent Ovarian Cancer
A Phase 1/2a Study to Evaluate the Tolerance, Safety, Efficacy, and Pharmacokinetics of Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) Using Paclitaxel for Platinum-resistant Recurrent Ovarian Cancer With Peritoneal Metastasis (PIPAC-OVPAC 1/2a)
Source: ClinicalTrials.gov · Last updated 9 Dec 2025
Brief summary (registry, in English)
The purpose of this study is to evaluate the tolerance, safety, efficacy, and pharmacokinetics of pressurized intraperitoneal aerosol chemotherapy (PIPAC) with paclitaxel in patients with platinum-resistant recurrent ovarian cancer and peritoneal carcinomatosis.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 1/2
- Study type
- Interventional
- Enrollment
- 53 (estimated)
- First submitted
- 5 May 2025
- Start date
- 1 Jan 2026
- Primary completion date
- 30 Apr 2030
- Lead sponsor
- Seoul National University Hospital
- Diseases
- Ovarian cancer
- NCT number
- NCT07273396
What you commit to
- Study type: Interventional · Phase 1/2
- Planned participants: 53
- From 1 Jan 2026 to the primary completion date, 30 Apr 2030
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- IV chemotherapy within 4 weeks prior to Cycle 1 PIPAC.
- Prior PIPAC therapy.
- Medically unfit for general anesthesia or laparoscopic surgery.
Other illness
- Hypersensitivity history to paclitaxel or PIPAC devices.
- Refusal of contraception:
- \- Medically acceptable methods:
- Intrauterine device (failure rate \<1%)
- Surgical sterilization (tubal ligation, hysterectomy, vasectomy; failure rate \<0.5%).
Lab values
- Uncontrolled comorbidities per investigator judgment:
- NYHA Class ≥II heart failure
- Clinically significant cardiovascular disease (e.g., arrhythmia, myocardial infarction)
- Immunosuppressive conditions (AIDS, autoimmune diseases, immunosuppressive therapy)
- Active HBV/HCV infection
- Uncontrolled hypertension (systolic \>160 mmHg or diastolic \>100 mmHg)
- Uncontrolled diabetes (HbA1c \>8%)
- Radiographic/clinical bowel obstruction.
Other
- ≥2 distant metastases (excluding retroperitoneal lymph nodes, pleural effusion, and localized skin metastases).
- Contraindications to paclitaxel per approved domestic labeling.
- Life expectancy \<3 months.
- Participation in another clinical trial within 1 month of screening.
- Other exclusionary factors per investigator discretion.
Who the study is looking for
- Age: Women aged 19-85 years.
- Diagnosis: Histologically confirmed ovarian, fallopian tube, or peritoneal cancer.
- Platinum Status:
- Refractory: Disease progression during platinum-based chemotherapy.
- Resistant: Progression within 6 months (24 weeks) post-platinum therapy.
- Prior Therapies: ≥2 prior intravenous chemotherapies (may include paclitaxel).
- Treatment Options: Unresponsive to/ineligible for standard therapies (e.g., intolerance, hypersensitivity) and ineligible for surgical resection.
- Measurable Disease: ≥1 measurable/evaluable peritoneal lesion per RECIST 1.1.
- Metastasis: ≤1 asymptomatic distant metastasis (excluding retroperitoneal lymph nodes, pleural effusion, localized skin metastases).
- Imaging Confirmation: Peritoneal carcinomatosis confirmed by PET-CT/CT.
- Performance Status: ECOG 0-2.
- Pregnancy/Contraception:
- Non-pregnant/non-lactating.
- Contraception: Effective methods (IUD, sterilization) for 6 months post-PIPAC (childbearing potential only).
- Organ Function:
- Bone Marrow: ANC \>1,500/mm³, platelets \>100,000/mm³, hemoglobin \>8.0 g/dL.
- Liver: Bilirubin ≤1.5×ULN, AST/ALT ≤1.5×ULN.
- Kidney: Creatinine ≤1.5×ULN, creatinine clearance \>60 mL/min.
- Lungs: FVC/FEV1 ≥70% predicted.
- Coagulation: INR ≤1.5, aPTT ≤1.5×ULN.
- Consent: Signed informed consent.
Age in the registry: 19 years to 85 years · Sex: Female · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.