Clinical trial · Interventional
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
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
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 Neoplasms | Ovarian Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Peritoneal Neoplasms | Peritoneal Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pressurized intraperitoneal aerosol chemotherapy (PIPAC) using paclitaxel | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- PIPAC-OVPAC group
- interventionNames
- Drug: Pressurized intraperitoneal aerosol chemotherapy (PIPAC) using paclitaxel
Primary outcomes (4)
- measure
- Dose limiting toxicities
- timeFrame
- Till 6 weeks after the first PIPAC in phase 1 study
- description
- Dose limiting toxicities
- measure
- Maximum tolerated dose
- timeFrame
- During phase 1 study (up to 6 weeks)
- description
- We consider dose escalation if 3 consecutive DLTs do not occur, or less than 1 in 6 DLTs occur, per standard 3+3 design. If DLT occurs in 2 or more of 6, the lower dose is considered the MTD if 1 or fewer DLTs are identified. In addition, the highest dose (140 mg/m2) is considered the MTD when 3 to 0 DLTs or 6 to 1 DLTs are identified at the highest dose. On the other hand, if the initial dose (20 mg/m2) is reduced to 10 mg/m2 to account for DLT, it is considered the MTD if no more than 1 in 6 develop DLT at that reduced dose.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 19 Years
- Maximum age
- 85 Years
Show eligibility criteria text
Inclusion Criteria:
1. Age: Women aged 19-85 years.
2. Diagnosis: Histologically confirmed ovarian, fallopian tube, or peritoneal cancer.
3. Platinum Status:
* Refractory: Disease progression during platinum-based chemotherapy.
* Resistant: Progression within 6 months (24 weeks) post-platinum therapy.
4. Prior Therapies: ≥2 prior intravenous chemotherapies (may include paclitaxel).
5. Treatment Options: Unresponsive to/ineligible for standard therapies (e.g., intolerance, hypersensitivity) and ineligible for surgical resection.
6. Measurable Disease: ≥1 measurable/evaluable peritoneal lesion per RECIST 1.1.
7. Metastasis: ≤1 asymptomatic distant metastasis (excluding retroperitoneal lymph nodes, pleural effusion, localized skin metastases).
8. Imaging Confirmation: Peritoneal carcinomatosis confirmed by PET-CT/CT.
9. Performance Status: ECOG 0-2.
10. Pregnancy/Contraception:
* Non-pregnant/non-lactating.
* Contraception: Effective methods (IUD, sterilization) for 6 months post-PIPAC (childbearing potential only).
11. 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.
12. Consent: Signed informed consent.
Exclusion Criteria:
1. ≥2 distant metastases (excluding retroperitoneal lymph nodes, pleural effusion, and localized skin metastases).
2. Contraindications to paclitaxel per approved domestic labeling.
3. Hypersensitivity history to paclitaxel or PIPAC devices.
4. 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.
5. IV chemotherapy within 4 weeks prior to Cycle 1 PIPAC.
6. Life expectancy \<3 months.
7. Prior PIPAC therapy.
8. Medically unfit for general anesthesia or laparoscopic surgery.
9. Refusal of contraception:
\- Medically acceptable methods:
* Intrauterine device (failure rate \<1%)
* Surgical sterilization (tubal ligation, hysterectomy, vasectomy; failure rate \<0.5%).
10. Participation in another clinical trial within 1 month of screening.
11. Other exclusionary factors per investigator discretion.References
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