Evaluation of TRC105 in the Treatment of Recurrent Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma

NCT ID: NCT01381861

Last Updated: 2019-03-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-07-31
• Study Completion Date: 2013-12-31

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of TRC105 in patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal carcinoma.

Detailed Description

Angiogenesis plays a central role in the progression of epithelial ovarian cancer. In mouse models, VEGF-inhibitors diminish ovarian tumor growth, metastasis and malignant ascites formation. Independent Phase 2 trials have demonstrated single-agent activity for bevacizumab in recurrent ovarian cancer, and randomized controlled Phase 3 trials are ongoing in the first-line setting (GOG 0218 and ICON-7) and for recurrent disease (GOG 0213, OCEANS).

TRC105 is an antibody to CD105, an important non-VEGF angiogenic target on vascular endothelial cells. TRC105 inhibits angiogenesis, tumor growth and metastases in preclinical models. In a Phase 1 study of advanced solid tumors, TRC105 therapy caused a global reduction in angiogenic biomarkers and reduced tumor burden at doses that were well-tolerated. We hypothesize that TRC105 will have single-agent activity in recurrent ovarian cancer. By targeting a non-VEGF pathway, TRC105 has the potential to complement VEGF inhibitors which could represent a major advance in ovarian cancer therapy.

Conditions

Recurrent Ovarian Cancer; Fallopian Tube Carcinoma; Primary Peritoneal Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Carotuximab (TRC105) alone

Single arm, open label Carotuximab (TRC105) alone therapy dosed at 10 mg/kg administered intravenously over 1 to 4 hours on days 1, 8, 15 and 22 of each 28 day cycle

Group Type: EXPERIMENTAL

Carotuximab (TRC105)

Intervention Type: BIOLOGICAL

Carotuximab (TRC105) 10 mg/kg weekly by intravenous administration on Days 1, 8, 15 and 22 of each 28-day cycle

Interventions

Carotuximab (TRC105)

Carotuximab (TRC105) 10 mg/kg weekly by intravenous administration on Days 1, 8, 15 and 22 of each 28-day cycle

Intervention Type: BIOLOGICAL

Other Intervention Names

TRC105; NSC#754227

Eligibility Criteria

Inclusion Criteria

• Recurrent epithelial ovarian, fallopian tube, or primary peritoneal carcinoma
• Measurable disease per RECIST 1.1
• At least one "target lesion" per RECIST 1.1
• Patients must have GOG Performance Status of 0 or 1
• Patients must have a life expectancy of ≥ 3 months
• Resolution of all acute toxic effects of prior therapy
• Free of active infection requiring antibiotics
• Must have had one prior platinum-based chemotherapeutic regimen for management of primary disease
• Patients could have received one additional cytotoxic regimen for management of recurrent disease
• Prior therapy directed at the malignant tumor, including hormonal and immunologic agents, must be discontinued at least three weeks prior to registration. Continuation of hormone replacement therapy is permitted.
• Adequate bone marrow function, renal function, hepatic function, neurologic function, blood coagulation parameters
• Negative serum pregnancy test and effective form of contraception for patients of childbearing potential

Exclusion Criteria

• Previous treatment with TRC105
• Current treatment on another therapeutic clinical trial
• Receipt of an investigational agent within 28 days of starting study treatment
• Serious, non-healing wounds, ulcers, or bone fractures.
• Active bleeding or pathologic conditions that carry a high risk of bleeding
• Patients with tumor involving major vessels or transmural bowel wall involvement by tumor
• Use of thrombolytic or anticoagulant agents (except heparin to maintain i.v. catheters) within 10 days prior to the first dose of TRC105
• History of deep venous thrombosis (DVT)(except patients who have received adequate anticoagulation are eligible, and may continue on anticoagulation if appropriate)
• History of peptic ulcer disease or erosive gastritis within the past 6 months
• Known active viral or nonviral hepatitis
• History or evidence of CNS disease
• Clinically significant cardiovascular disease
• Known hypersensitivity to Chinese hamster ovary cell products or other recombinant human, chimeric, or humanized antibodies
• Pregnant or nursing
• Under the age of 18
• Patients with or with anticipation of invasive procedures including major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to treatment with TRC105
• History of other invasive malignancies, except non-melanoma skin cancer and other cancers that have been treated with no evidence of disease within the last 3 years
• History of primary endometrial cancer diagnosed within the last 5 years, unless all of the following conditions are met: Stage not greater than I-B; no more than superficial myometrial invasion, without vascular or lymphatic invasion; no poorly differentiated subtypes, including papillary serous, clear cell or other FIGO Grade 3 lesions
• Patients who have received prior chemotherapy for any abdominal or pelvic tumor OTHER THAN for the treatment of ovarian, fallopian tube, or primary peritoneal cancer within the last five years are excluded. Patients may have received prior adjuvant chemotherapy for localized breast cancer, provided that it was completed > 3 years prior to registration, and patient remains free of recurrent or metastatic disease
• Prior radiotherapy to any portion of the abdominal cavity or pelvis
• Patients with clinical symptoms or signs of gastrointestinal obstruction and who require parenteral hydration and/or nutrition

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tracon Pharmaceuticals Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Charles P Theuer, MD

Role: STUDY_DIRECTOR

TRACON Pharmaceuticals

Locations

University of Alabama at Birmingham

Birmingham, Alabama, United States

University of California, San Diego

La Jolla, California, United States

University of Southern California

Los Angeles, California, United States

Palm Beach Cancer Institute

West Palm Beach, Florida, United States

Indiana University-Bren and Melvin Simon Cancer Center

Indianapolis, Indiana, United States

Memorial Sloan-Kettering Cancer Center

New York, New York, United States

MD Anderson Cancer Center

Houston, Texas, United States

Countries

United States

Other Identifiers

105OC201

Identifier Type: -

Identifier Source: org_study_id