Active, not recruiting • Phases I, II • Stage IV • Medical Oncology • Post-Menopausal • Interventional
The following is imported from ClinicalTrials.gov:
A Phase 1b/2 Study of Rebastinib (DCC-2036) in Combination With Paclitaxel in Patients With Advanced or Metastatic Solid Tumors
This is an open-label Phase 1b/2 multicenter study of rebastinib (DCC-2036) in combination with paclitaxel designed to evaluate the safety, tolerability, and pharmacokinetics (PK) in patients with advanced or metastatic solid tumors.
Actual study start date:
September 19, 2018
Ages eligible for study:
18 - 999
Sexes eligible for study:
Arms and Intervention
Male or female patients ≥18 years of age at the time of informed consent.
Part 1 Histologically confirmed diagnosis of a locally advanced or metastatic solid tumor for which paclitaxel is considered appropriate treatment.
Triple-negative and Stage IV inflammatory breast cancer.
Recurrent ovarian cancer.
Recurrent, metastatic or high-risk endometrial cancer.
Advanced (stage III or IV), or recurrent gynecological carcinosarcoma
Homologous or heterologous type carcinosarcoma (malignant mixed Mullerian tumor [MMMT] allowed
ECOG PS of ≤2.
Able to provide an archival tumor tissue sample
Adequate organ function and bone marrow reserve
If a female of childbearing potential, must have a negative pregnancy test prior to enrollment.
Patient must provide signed consent to participate in the study and is willing to comply with study-specific procedures.
Received prior anticancer or other investigational therapy within 28 days or 5× the half-life prior to the first dose.
Not recovered from prior-treatment toxicities to Grade ≤1.
Peripheral neuropathy of any etiology >Grade 1.
Known active CNS metastases.
Use of systemic corticosteroids.
Known retinal neovascularization, macular edema or macular degeneration.
History or presence of clinically relevant cardiovascular abnormalities.
QTcF >450 ms in males or >470 ms in females.
Left ventricular ejection fraction (LVEF) <50% at screening.
Arterial thrombotic or embolic events.
Venous thrombotic event.
Active infection ≥Grade 3.
HIV or HCV infection only if taking medications excluded per protocol, active HBV, or active HCV infection.
Use of proton pump inhibitors.
If female, the patient is pregnant or lactating.
Major surgery 4 weeks prior to the first dose of study drug
Malabsorption syndrome or other illness which could affect oral absorption.
Known allergy or hypersensitivity to any component of rebastinib or any of its excipients.