Dose Escalation Study of BIBF 1120 in Combination With Carboplatin and PLD in Relapsed Ovarian Cancer (OC)

• Status: Terminated
• Trial end date: 2012-10-01
• Target enrollment: 0
• Participant gender: Female

Summary

This phase I, open label dose escalation study will investigate the addition of BIBF 1120 to treatment with the combination of carboplatin and Pegylated Liposomal Doxorubicin (PLD) in patients with advanced, platinum sensitive relapsed ovarian cancer, fallopian tube carcinoma or primary peritoneal cancer. Patients will be treated with BIBF 1120 together with carboplatin and PLD in up to 6-9 repeated 28 days treatment courses until disease progression is observed.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Boehringer Ingelheim
• Treatments: Carboplatin; Liposomal doxorubicin; Nintedanib

Criteria

Inclusion criteria:

1. Female patients, age 20 years or older, with relapse of histologically (on initial diagnosis) confirmed epithelial ovarian cancer, fallopian tube carcinoma or primary peritoneal cancer

2. Up to 3 lines of prior chemo therapy, with treatment free interval of >6 months

3. Platinum based chemotherapy in the immediately preceding line.

4. Eastern Cooperative Oncology Group (ECOG) performance score 0 or 1

5. Written informed consent that is consistent with Good Clinical Practice (GCP) guidelines

Exclusion criteria:

1. Prior chemotherapy with PLD, and any contraindication for therapy with carboplatin or PLD.

2. More than 2 lines of prior therapies that contained angiogenesis inhibitor.

3. Patients for whom surgery is planned, e.g. interval debulking surgery.

4. History of a cerebral vascular accident, transient ischemic attack or subarachnoid haemorrhage within the past 6 months.

5. Serious infections in particular if requiring systemic antibiotic (antimicrobial, antifungal) or antiviral therapy.

6. Laboratory values indicating an increased risk for adverse events.

7. Significant cardiovascular diseases.