Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Doxorubicin)

AbbVie (prior sponsor, Abbott)138 enrolled

Overview

This is an open-label study of liposomal doxorubicin with or without volociximab for the treatment of subjects with advanced epithelial ovarian cancer or primary peritoneal cancer relapsed after prior therapy with Plat/Taxane-based chemo. Volociximab is an anti-angiogenic integrin inhibitor being developed for the treatment of solid tumors. Preclinical data with a surrogate volociximab antibody administered as monotherapy indicate encouraging efficacy in terms of tumor reduction and anti-angiogenic effects in mouse ovarian cancer xenograft models. In clinical studies, volociximab has been evaluated in several solid tumor types, including pancreatic, renal, and melanoma, with many subjects who entered the studies with progressive disease remaining progression-free for several months. In all studies in solid tumors, volociximab has shown a favorable safety profile when administered at 10 mg/kg q2wks and more recently at 15 mg/kg qwk. A study of volociximab in combination with liposomal doxorubicin in subjects with ovarian cancer or primary peritoneal cancer who have relapsed after prior platin/taxane therapies is warranted to further evaluate the drug's efficacy and safety. The investigators have thus far activated stage 2 of this study at 11/25 sites. Worldwide, the study aims to enroll 150 subjects.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Interventions

M200 (Volociximab)DRUG

7.5 mg/kg, IV infusion every week until disease progression

Liposomal DoxorubicinDRUG

40 mg/m2, IV infustions every 4 weeks until disease progression, the maxium number of doses a subject can receive is 12.

M200 (Volociximab)DRUG

15 mg/kg, IV infusions every week until disease progression

M200 (Volociximab)DRUG

15 mg/kg, IV infustions every other week until disease progression

Eligibility

Sex: FEMALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Females aged \>= 18 years old at the time of informed consent. * Advanced (Stage III or IV) histologically documented epithelial ovarian cancer or primary peritoneal cancer (excluding small, round-cell histologies). * Recurrent or persistent disease. * Received no more than 2 prior cancer treatment regimens, at least one of which must have included a platinum/taxane based therapy. If the same regimen is given more than once, it will count as one regimen. If components of a regimen are given more than once using the same schedule, it will count as one regimen. * At least 1 target lesion to assess response by RECIST criteria. (Tumors within a previously irradiated field are designated as non-target) * Other protocol-defined inclusion criteria apply. Exclusion Criteria: * Subjects taking immunomodulatory agents including, but not limited to, interferons, interleukins, systemic steroids, cyclosporine, tacrolimus, calcineurin inhibitors, chronic low dose methotrexate, or azathioprine. (Use of inhaled or intranasal steroids or oral steroids 10 mg/day prednisone or its equivalent are permitted.) * Subjects who require treatment with an anti coagulant with the exception of low dose Aspirin® (81 mg/day), warfarin (1 mg/day), or heparin for IV catheter patency * Evidence of bleeding diathesis or coagulopathy. (Prior history of DVT will not exclude subjects from participating in this study.) * History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day 1. * Non-healing wound, ulcer, or bone fracture. * Evidence of autoimmune disease including, but not limited to, ulcerative colitis, Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus, scleroderma, and other disease in which immune function or immune competence is known to be impaired. * Active infection requiring systemic antibiotics, antivirals, or antifungals including HIV/AIDS, hepatitis B, or hepatitis C infection. * Other protocol-defined exclusion criteria apply

Locations (39)

Site Reference ID/Investigator# 75281

Anaheim, California, United States

Site Reference ID/Investigator# 75275

Redondo Beach, California, United States

Site Reference ID/Investigator# 75296

Sunrise, Florida, United States

Site Reference ID/Investigator# 75299

Atlanta, Georgia, United States

Site Reference ID/Investigator# 75300

Savannah, Georgia, United States

Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Doxorubicin)

Overview

Conditions

Interventions

Eligibility

Locations (39)

Outcomes

Primary Outcomes