Clinical trial · Interventional
Study of Paclitaxel in Patients With Ovarian Cancer
An Open, Randomized, Multicenter Study in Patients With Recurrent Epithelian Cancer, Primary Peritoneal Cancer or Fallopian Tube Cancer to Compare the Efficay and Safety of Paclitaxel (Micellar) Nanoparticles and Paclitaxel (Cremophor® EL)
- 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)
RATIONALE: Paclitaxel is one of the most widely used human anticancer agents. Paclitaxel has a low degree of solubility and Cremophor EL is typically used as the solubiliser. Cremophor EL is known to cause hypersensitivity reactions that can be life-threatening. As Paclical® does not contain Cremophor EL, hypersensitivity reactions can be expected to be less. PURPOSE: To study the efficay and safety of two different formulations of paclitaxel, Paclical® and Taxol®.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Epithelial Ovarian Cancer | Ovarian Carcinoma | ALIAS | 0.90 |
| Fallopian Tube Cancer | Malignant Fallopian Tube Neoplasm | ALIAS | 0.90 |
| Primary Peritoneal Cancer | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Paclical® | Drug | — | UNRESOLVED |
| Taxol® | Drug | Taxol | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Paclitaxel, micellar (Paclical®)
- interventionNames
- Drug: Paclical®
- type
- ACTIVE_COMPARATOR
- label
- Paclitaxel, CrEL (Taxol®)
- interventionNames
- Drug: Taxol®
Primary outcomes (3)
- measure
- Progression free survival (PFS).
- measure
- Change in Area under the curve of CA 125
- measure
- Incidence and severity of hypersensitivity reactions
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histological or cytological confirmed epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer. * Patients relapsing \> 6 months after end of first line or second line treatment including platinum based therapy. Prior therapy and duration of response will be documented in the CRF for descriptive analysis. * CA 125 \>2 x upper normal limit (UNL) documented at two occasions, with more than one week interval, according to appendix I, patient groups A and B, measurable/non- measurable disease. * Age \> 18 years * Eastern Cooperative Oncology Group (ECOG) performance score 0-2 * Life expectancy \>12 weeks * Patient has blood counts at baseline of: * Absolute neutrophil count (ANC) \>1,5 x 109 / L. * Platelet count \>100 x 109 / L * Haemoglobin (Hb) ≥9g/dl (can be post transfusion) * Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) \< 2 x UNL * Total bilirubin ≤1.5 x UNL. * Adequate renal function defined as serum creatinine \< 2.0 mg/dl or 177μmol/l. * Alkaline phosphatase (ALP) \< 2.5 x UNL * Signed informed consent obtained Exclusion Criteria: * Patient has peripheral neuropathy of grade ≥ 2 per NCI-CTCAE version 3.0 * Surgical procedure due to progressive disease within 4 weeks of any of the CA-125 measurements * Patient receiving concurrent hormonal, immuno-, or radiotherapy. Treatment must have stopped for at least 4 weeks before start of drug treatment (Day 1, Cycle 1). * Bowel obstruction at screening * Tumours of other origin or histology * Patient of child-bearing potential, not practising adequate contraception, or pregnant or lactating women * Patient has a history of severe allergy or severe hypersensitivity to study drugs * Any uncontrolled medical problem that in the opinion of the investigator would preclude safe administration of the study drugs, e.g. heart, lung or kidney disease, suspicion of brain metastasis or mental disorder to make the patient unable to participate in the study * Participation in an investigational drug study within 4 weeks prior to study treatment (Day 1, Cycle 1)
References
Publications (1)
- DERIVEDVergote I, Bergfeldt K, Franquet A, Lisyanskaya AS, Bjermo H, Heldring N, Buyse M, Brize A. A randomized phase III trial in patients with recurrent platinum sensitive ovarian cancer comparing efficacy and safety of paclitaxel micellar and Cremophor EL-paclitaxel. Gynecol Oncol. 2020 Feb;156(2):293-300. doi: 10.1016/j.ygyno.2019.11.034. Epub 2019 Dec 9. PMID 31826802