Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone to Treat Metastatic Breast Cancer

This study has been completed.
Sponsor:
Collaborator:
Genentech, Inc.
Information provided by (Responsible Party):
AbbVie ( AbbVie (prior sponsor, Abbott) )
ClinicalTrials.gov Identifier:
NCT00645177
First received: March 24, 2008
Last updated: January 23, 2013
Last verified: January 2013

March 24, 2008
January 23, 2013
July 2008
December 2009   (final data collection date for primary outcome measure)
Progression-free survival [ Time Frame: Radiographic evaluation every 3 months, clincial evaluation monthly ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00645177 on ClinicalTrials.gov Archive Site
Overall survival [ Time Frame: Subject death ] [ Designated as safety issue: No ]
  • Overall survival [ Time Frame: Subject death ] [ Designated as safety issue: No ]
  • Safety [ Time Frame: every cycle (28 days) ] [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone to Treat Metastatic Breast Cancer
A Phase 2 Randomized, Placebo-Controlled, Double-Blind Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone as First-line Treatment in Subjects With Locally Recurrent or Metastatic Breast Cancer

The purpose of this study is to determine the effect of ABT-869 plus paclitaxel compared to paclitaxel alone on disease progression in metastatic breast cancer.

Only the open-label lead-in portion of the study was enrolled (n=10). The randomized portion was not initiated. N = approximately 102 (90 randomized in a 1:1 ratio in Phase 2, approximately 6-12 enrolled in open-label lead-in to assess the tolerability of the combination) Phase 2, randomized, placebo-controlled, double-blind, multi-center study of the efficacy and tolerability of the ABT-869 + paclitaxel versus placebo for ABT-869 + paclitaxel in subjects with documented metastatic breast cancer in the first line metastatic therapy setting. An initial open-label, lead-in cohort of six subjects will be monitored for 2 cycles (8 weeks) to assess the PK interactions and the safety of the combination of 0.20 mg/kg QD ABT-869 and paclitaxel (90 mg/m2). Enrollment into the randomized portion will begin after a cohort has completed two cycles (8 weeks) of therapy and no toxicities prohibit the cohort from continuing on to Cycle 3. Alternative doses may be explored based on the tolerability of the combination.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Metastatic Breast Cancer
  • Drug: ABT-869
    0.20 mg/kg (or dose from Lead-in) QD, tablets taken orally days 1-28 of every 28-day cycle
  • Drug: paclitaxel
    90 mg/m2 IV infusion over 1 hour, weekly every 3 out of 4 weeks
  • Drug: Placebo for ABT-869
    0.20 mg/kg (or dose from Lead-in) QD, tablets taken orally days 1-28 of every 28-day cycle
  • Active Comparator: A

    In study, this arm is a randomized (blinded) to ABT-869 arm plus paclitaxel.

    Note: Prior to randomization, approximately 6-12 subjects will be enrolled in open-label lead-in to assess the tolerability of the combination. The initial open-label, lead-in cohort of six subjects will be monitored for 2 cycles (8 weeks) to assess the PK interactions and the safety of the combination of 0.20 mg/kg QD ABT-869 and paclitaxel (90 mg/m2). Enrollment into the randomized portion will begin after a cohort has completed two cycles (8 weeks) of therapy and no toxicities prohibit the cohort from continuing on to Cycle 3.

    Alternative doses may be explored based on the tolerability of the combination

    Interventions:
    • Drug: ABT-869
    • Drug: paclitaxel
  • Placebo Comparator: B

    In study, this arm is a randomized (blinded) to placebo for ABT-869 plus paclitaxel arm.

    Note: Prior to randomization, approximately 6-12 subjects will be enrolled in open-label lead-in to assess the tolerability of the combination. The initial open-label, lead-in cohort of six subjects will be monitored for 2 cycles (8 weeks) to assess the PK interactions and the safety of the combination of 0.20 mg/kg QD ABT-869 and paclitaxel (90 mg/m2). Enrollment into the randomized portion will begin after a cohort has completed two cycles (8 weeks) of therapy and no toxicities prohibit the cohort from continuing on to Cycle 3.

    Alternative doses may be explored based on the tolerability of the combination

    Interventions:
    • Drug: paclitaxel
    • Drug: Placebo for ABT-869
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
December 2009
December 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Subject must be female and > 18 years of age.
  • Subject must be diagnosed with adenocarcinoma of the breast.
  • Subject must have metastatic disease or locally recurrent disease that is not amenable to surgical resection with curative intent.
  • No prior chemotherapy for locally recurrent or metastatic breast cancer.
  • At least 12 months since prior adjuvant or neoadjuvant chemotherapy (including prior taxane therapy and prior anti-angiogenic therapy [i.e. bevacizumab or a TKI]).
  • No HER-2 -over-expression (3+) breast cancer (unless treated with trastuzumab or lapatinib).
  • Subject has measurable disease by RECIST criteria (randomized portion only).
  • Eastern Cooperative Oncology Group (ECOG) Performance Score of 0-1.
  • Subject must have adequate bone marrow, renal and hepatic function.
  • Subject must have PTT < 1.5 x ULN and INR < 1.5.

Exclusion Criteria:

  • Subject has received anti-cancer therapy (other than chemotherapy) including investigational agents, or biologic therapy within 21 days or within a period defined by 5 half lives, whichever is shorter, prior to Study Day 1.
  • Subject has not recovered to less than or equal to grade 1 clinically significant adverse effects/toxicities of the previous therapy.
  • Subject has received radiation therapy within 14 days of Study Day 1.
  • Subject has received anti-cancer hormonal therapy within 14 days of Study Day 1.
  • Subject has undergone major surgery within 21 days of Study Day 1.
  • The subject has untreated brain or meningeal metastases.
  • Subject is receiving therapeutic anticoagulation therapy.
  • Subject has a history of or currently exhibits clinically significant cancer related events of bleeding (e.g., hemoptysis).
  • Subject currently exhibits symptomatic or persistent, uncontrolled hypertension.
  • Subject has a history of myocardial infarction, stroke, or transient ischemic attack (TIA) within 6 months of study day 1.
  • Subject has a documented left ventricular (LV) ejection fraction < 50%
  • Subject has known autoimmune disease with renal involvement.
Female
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Mexico,   United States
 
NCT00645177
M10-265, 2007-005905-23
Not Provided
AbbVie ( AbbVie (prior sponsor, Abbott) )
AbbVie (prior sponsor, Abbott)
Genentech, Inc.
Study Director: Justin L. Ricker, MD AbbVie
AbbVie
January 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP