A Clinical Study to Compare Efficacy and Safety of Two Formulations ofPaclitaxel in Patients with Recurrent Epithelial Ovarian Cancer, PrimaryPeritoneal Cancer or Fallopian Tube Cancer.

• Conditions: Therapeutic area: Diseases [C] - Cancer [C04]; Histological or cytological confirmed epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer.; MedDRA version: 15.0Level: LLTClassification code 10052171Term: Peritoneal carcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); MedDRA version: 15.0Level: PTClassification code 10016180Term: Fallopian tube cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); MedDRA version: 15.0Level: PTClassification code 10066697Term: Ovarian cancer recurrentSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)

• Registration Number: EUCTR2008-002668-32-LT
• Lead Sponsor: Oasmia Pharmaceutical AB

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-03-17
• Last Update Posted: 3 February 2014

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: Female
• Target Recruitment: 850

Inclusion Criteria

1.Histological or cytological confirmed epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer.
2.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.
3.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.
4.Age > 18 years
5.Eastern Cooperative Oncology Group (ECOG) performance score 0-2
6.Life expectancy >12 weeks

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 10
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 15

Exclusion Criteria

1.Patient has peripheral neuropathy of grade = 2 per NCI- CTCAE version 3.0
2.Surgical procedure due to progressive disease within 4 weeks of any of the CA- 125 measurements
3.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).
4.Bowel obstruction at screening

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified