Skip to main content
OpenTrials
Completed

NCT Number: NCT01121406

BI 6727 (Volasertib) Randomised Trial in Ovarian Cancer

This is an international, randomized phase II trial. The aim is to assess the efficacy and the safety of BI 6727 Versus investigator's best choice single agent cytotoxic in recurrent third and fourth lines platinum resistant/refractory ovarian cancer.

100 patients will be randomised at the study entry to receive either BI 6727 (Arm A: 50 patients) or non-platinum single agent cytotoxic (Arm B: 50 patients) Treatment will be continued until disease progression or unacceptable toxicity. Primary endpoint: disease control rate at week 24 according to Response Evaluation Criteria In Solid Tumours version 1.1.

Secondary endpoints: efficacy (progression free survival, overall survival, biological tumour response, biological progression free survival assessed by serum CA 125 according to Gynecologic Cancer Intergroup criteria, safety according to the NCI CTCAE v.3, disease symptoms control assessed by the EORTC QLQ-C30, QLQ-OV28 and individual symptoms questionnaires, pharmacokinetics of BI 6727.

Others endpoints: biomarkers and pharmacogenetics analysis (optional)

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Ovarian Neoplasms Adnexal Diseases Endocrine Gland Neoplasms Endocrine System Diseases Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Genital Diseases Genital Diseases, Female Genital Neoplasms, Female Gonadal Disorders Neoplasms Neoplasms by Site Ovarian Diseases Urogenital Diseases Urogenital Neoplasms

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

1230.18.32003 Boehringer Ingelheim Investigational Site, Brussels, Belgium

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed recurrent epithelial ovarian carcinoma, peritoneal carcinoma or fallopian tube carcinoma.
  • Platinum resistant or platinum refractory disease.
  • Eastern Collaborative Oncology Group performance status < = 2.
  • Life expectancy > = 3 months.
  • At least one measurable lesion (Response Evaluation Criteria In Solid Tumours version 1.1).
  • Adequate hepatic, renal and bone marrow functions.
  • signed written informed consent prior to admission to the study.

Exclusion criteria

  • Contre-indications for cytotoxic treatment according to the Summary of Product Characteristics (Arm B).
  • Clinical evidence of active brain metastasis or leptomeningeal involvement.
  • Other malignancy currently requiring active therapy.
  • QTc prolongation according to Fridericia formula deemed clinically relevant by the investigator (e.g., congenital long QT syndrome, QTc according to Fridericia formula > 470 ms).
  • Hypersensitivity to one of the trial drugs or the excipients.
  • Serious illness or concomitant non- oncological disease.
  • Systemic anticancer therapy within 4 weeks before the start of the study.
  • Evidence of ileus sor sub ileus.

Treatment and study plan

paclitaxel

Drug

Patients receive paclitaxel in a 4 week schedule

Gemcitabine

Drug

Patients receive gemcitabine in a 3 week schedule

Topotecan

Drug

Patients receive topotecan in 3 or 4 week schedule

Pegylated Liposomal Doxorubicin (PLD)

Drug

Patients receive PLD in a 4 week schedule

BI 6727

Drug

Patients receive BI 6727 infusion every 3 weeks

Primary outcomes

  1. Disease Control Rate (DCR) at Week 24 According to Response Evaluation Criteria In Solid Tumours (RECIST) Version 1.1

    Time frame: Week 24

    DCR was defined as the proportion of patients who had an overall response of complete response (CR), partial response (PR), or stable disease (SD).

Secondary outcomes

  1. Progression Free Survival (PFS)

    Time frame: From randomization until disease progression, death or study discontinuation; Up to 213 weeks

    Progression-free survival of a patient was based on the investigator's assessment; it was defined as the number of days from the date of randomisation until the date of either disease progression or death from any cause, whichever occurred first.

    Definition of disease progression according to RECIST version 1.1; Patients with measurable tumour lesions at baseline, Target-lesions: at least a 20% increase in the sum of diameters of target lesions, the sum of diameters must also demonstrate an absolute increase of at least 5 mm,taking as reference the smallest sum on study, or appearance of 1 or more new lesions.

    Non-target lesions: unequivocal progression of existing non-target lesions or appearance of 1 or more new lesions Patients with non-measurable tumour lesions at baseline, Non-target lesions: requires unequivocal progression of existing non-target lesions or appearance of 1 or more new lesions

  2. Overall Survival (OS)

    Time frame: From randomization until death or study discontinuation; Up to 213 weeks

    OS is defined as time from randomisation to death irrespective of the cause of the death.

  3. Best Overall Response

    Time frame: time from the date of randomisation until study completion/discontinuation; Up to 213 weeks

    Best overall response (BOR) is defined as the best response recorded at any time from the date of randomisation until the end of treatment.

    Missing categories signify that no tumour imaging has been performed post baseline, and therefore the response status could not be assessed.

  4. Biological Tumour Response Based on Serum Cancer Antigen 125 (CA-125) According to the Gynaecologic Cancer Intergroup (GCIG) Criteria

    Time frame: At screening and every 6 weeks thereafter (Up to 213 weeks)

    Patients were to have a pre-treatment CA-125 of at least twice the upper limit of normal to be considered for CA-125 response. Patients were not evaluable by CA-125 if they had received mouse antibodies or if they had undergone medical and/or surgical interference with their peritoneum or pleura during the previous 28 days. In eligible patients, a CA-125 response was defined as the moment the CA- 25 was reduced by 50%, with this being confirmed with a consecutive CA-125 assessment not earlier than 28 days after the previous one.

    Biological response rate based on serum CA-125 levels was assessed according to the guidelines by the Gynaecologic Cancer Intergroup. Monitoring of blood levels of the tumour marker CA-125 was performed at screening and every 6 weeks thereafter.

  5. Biological Progression-free Survival Based on Serum Cancer Antigen 125 (CA-125) According to the Gynaecologic Cancer Intergroup (GCIG) Criteria

    Time frame: At screening and every 6 weeks thereafter (Up to 213 weeks )

    Biological PFS including assessment of CA-125 levels was defined as the time from randomisation until the first occurrence of progressive disease according to CA-125, progressive disease according to radiological evidence, or death.

    Also according to the below criterias,

    • In patients with radiological measurable disease, disease progression during study treatment could not be declared on the basis of CA-125 alone.
    • Patients with elevated CA-125 pre-treatment and normalization of CA-125 had to show evidence of CA-125 ≥ to two times the upper normal limit on two occasions at least one week apart or
    • Patients with elevated CA-125 pre-treatment, which never normalized, had to show evidence of CA-125 ≥ to two times the nadir value on two occasions at least one week apart or
    • Patients with CA-125 in the normal range pre-treatment had to show evidence of CA-125 ≥ to two times the upper normal limit on two occasions at least one week apart.

  6. Time to Deterioration in Global Health Status/Quality of Life (QOL)

    Time frame: Every 6 weeks (Up to 213 weeks )

    Time to deterioration in global health status/Quality of life (QOL) and symptom control assessed by the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, QLQ-OV28, and individual symptom questionnaires.

    The time to deterioration was defined as the time from randomisation to a score increased (i.e. worsened) by at least 10 points from baseline (0-100 point scale). If score is missing, and patient died within 28 days after scheduled time for completion, the patient was considered deteriorated. In this case, time to deterioration is time to death.

  7. Time to Deterioration in Fatigue/Quality of Life (QOL)

    Time frame: Every 6 weeks (Up to 213 weeks )

    Time to deterioration in fatigue/Quality of life (QOL) and symptom control assessed by the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, QLQ-OV28, and individual symptom questionnaires.

    The time to deterioration was defined as the time from randomisation to a score increased (i.e. worsened) by at least 10 points from baseline (0-100 point scale). If score is missing, and patient died within 28 days after scheduled time for completion, the patient was considered deteriorated. In this case, time to deterioration is time to death.

  8. Time to Deterioration in Pain/ Quality of Life (QOL)

    Time frame: Every 6 weeks (Up to 213 weeks )

    Time to deterioration in pain/ Quality of life (QOL) and symptom control assessed by the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, QLQ-OV28, and individual symptom questionnaires.

    The time to deterioration was defined as the time from randomisation to a score increased (i.e. worsened) by at least 10 points from baseline (0-100 point scale). If score is missing, and patient died within 28 days after scheduled time for completion, the patient was considered deteriorated. In this case, time to deterioration is time to death.

  9. Time to Deterioration in Abdominal Bloating/ Quality of Life (QOL)

    Time frame: Every 6 weeks (Up to 213 weeks )

    Time to deterioration in abdominal bloating/ Quality of life (QOL) and symptom control assessed by the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, QLQ-OV28, and individual symptom questionnaires.

    The time to deterioration was defined as the time from randomisation to a score increased (i.e. worsened) by at least 10 points from baseline (0-100 point scale). If score is missing, and patient died within 28 days after scheduled time for completion, the patient was considered deteriorated. In this case, time to deterioration is time to death.

  10. Time to Deterioration in the Three Most Troublesome Disease Specific Symptoms/ Quality of Life (QOL)

    Time frame: Every 6 weeks (Up to 213 weeks)

    Three most troublesome disease specific symptoms, defined by the patient at baseline.

    Patients that have defined more than 3 most troublesome symptoms have not been taken into account in the analysis.

    Quality of life (QOL) and symptom control assessed by the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, QLQ-OV28, and individual symptom questionnaires.

    The time to deterioration was defined as the time from randomisation to a score increased (i.e. worsened) by at least 10 points from baseline (0-100 point scale). If score is missing, and patient died within 28 days after scheduled time for completion, the patient was considered deteriorated. In this case, time to deterioration is time to death.

  11. Incidence and Intensity of Adverse Events According to the United States National Cancer Institute (US NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0

    Time frame: From first treatment administration to 21 days after the last drug administration (Up to 1403 days)

    Incidence and intensity of adverse events according to the United States National Cancer Institute (US NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0

  12. Clinically Relevant Changes in Laboratory and ECG Data

    Time frame: From first treatment administration to 21 days after the last drug administration (Up to 1403 days)

    Clinically relevant changes in laboratory and ECG data

  13. AUC (0-24); Area Under the Concentration-time Curve in Plasma Over the Time Interval From 0 to 24 Hours for BI 6727 BS

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    AUC (0-24); area under the concentration-time curve in plasma over the time interval from 0 to 24 hours for BI 6727 BS

  14. AUC (0-24); Area Under the Concentration-time Curve in Plasma Over the Time Interval From 0 to 24 Hours for CD 10899 BS

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    AUC (0-24); area under the concentration-time curve in plasma over the time interval from 0 to 24 hours for CD 10899 BS (metabolite of Volasertib BI 6727)

  15. AUC (0-inf); Area Under the Concentration-time Curve in Plasma Over the Time Interval From 0 Extrapolated to Infinity for BI 6727 BS

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    AUC (0-inf); area under the concentration-time curve in plasma over the time interval from 0 extrapolated to infinity for BI 6727 BS

  16. AUC (0-inf); Area Under the Concentration-time Curve in Plasma Over the Time Interval From 0 Extrapolated to Infinity for CD 10899 BS

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    AUC (0-inf); area under the concentration-time curve in plasma over the time interval from 0 extrapolated to infinity for CD 10899 BS (metabolite of Volasertib BI 6727)

  17. Cmax; Maximum Measured Concentration of BI 6727 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    Cmax; maximum measured concentration of BI 6727 BS in plasma

  18. Cmax; Maximum Measured Concentration of CD 10899 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    Cmax; maximum measured concentration of CD 10899 BS (metabolite of Volasertib BI 6727) in plasma

  19. Tmax; Time From Dosing to Maximum Measured Concentration of BI 6727 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    tmax; time from dosing to maximum measured concentration of BI 6727 BS in plasma

  20. Tmax; Time From Dosing to Maximum Measured Concentration of CD 10899 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    tmax; time from dosing to maximum measured concentration of CD 10899 BS (metabolite of Volasertib BI 6727) in plasma

  21. t1/2; Terminal Half-life of BI 6727 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    t1/2; Terminal half-life of BI 6727 BS in plasma

  22. t1/2; Terminal Half-life of CD 10899 BS in Plasma

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    t1/2; Terminal half-life of CD 10899 BS in plasma

  23. MRT; Mean Residence Time of BI 6727 BS in the Body

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    MRT; Mean residence time of BI 6727 BS in the body

  24. CL; Total Clearance of BI 6727 BS in Plasma After Intravenous Administration

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    CL; total clearance of BI 6727 BS in plasma after intravenous administration

  25. Vss;Apparent Volume of Distribution at Steady State Following Intravenous Administration for BI 6727 BS

    Time frame: -0.083 hours (h), 2h, 4h, 6h, 24h, 168h and 336 h after first drug administration

    Vss;apparent volume of distribution at steady state following intravenous administration for BI 6727 BS

  26. Biomarkers and Pharmacogenetics Analysis (Optional)

    Time frame: 6 months

    This endpoint has not been statistically analysed in the study report

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

Phase II Randomized Trial of the Polo-like Kinase 1 Inhibitor BI 6727 Monotherapy Versus Investigator´s Choice Chemotherapy in Ovarian Cancer Patients Resistant or Refractory to Platinum-based Cytotoxic Therapy

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
May 12, 2010
Registry last updated
Aug 13, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.