A Study of LCL161 in Combination With Weekly Paclitaxel in Adult Patients With Advanced Solid Tumors

Completed · Phase 1

Conditions studied: Solid Tumors

In brief

This is a dose escalation study that will assess the safety and efficacy of LCL161 in combination with weekly paclitaxel in adult patients with advanced solid tumors.

Key facts

Study ID

NCT01240655

Run by

Novartis Pharmaceuticals

People needed

76

Starts

2011-04-01

Expected to finish

2015-01-01

Last updated by the study team

2020-12-19

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with breast cancer must have a histologically or cytologically confirmed diagnosis of disease that has metastasized or is resistant to therapy.
• Patients with ovarian cancer must have histological evidence of recurrent epithelial ovarian, fallopian tube or peritoneal cancer.
• Patients must have recovered or stabilized from all toxicities related to their previous treatment except for alopecia Male or female patients 18 years or older ECOG performance status 0-1 Life expectancy greater than 12 weeks Measurable disease as determined by RECIST v1.0 Patients must give written informed consent and comply with the protocol

You may not qualify if…

• For patients with breast cancer:
• Concurrent Her2-directed or anti-estrogen therapy
• For patients with ovarian cancer:
• Primary refractory disease, defined as progression during initial treatment with a platinum- and taxane-containing regimen.
• Prior treatment with weekly paclitaxel. More than two chemotherapy regimens given in the relapse setting. Evidence of a documented bowel obstruction within six months of study entry Patients with unresolved peripheral neuropathy, nausea, vomiting, or diarrhea ≥ CTCAE Grade 2 Any concurrent severe and/or uncontrolled medical conditions that could increase the patient's risk for toxicity while in the study or that could confound discrimination between disease- and study treatment-related toxicities.
• Patients with impairment of GI function or GI disease that may significantly alter the absorption of LCL161 Patients who have undergone major surgery ≤ 3 weeks prior to starting study drug or who have not recovered from side effects of procedure.
• Pregnant or breast feeding (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive β-HCG laboratory test (> 5 mIU/mL).
• Known diagnosis of human immunodeficiency virus (HIV) infection or chronic active hepatitis B or C (HIV and hepatitis testing are not mandatory).
• Other protocol-defined inclusion/exclusion criteria may apply

Where it is running

• Dana Farber Cancer Institute SC — Boston, Massachusetts, United States
• University of North Carolina Lineberger Comp Cancer Ctr — Chapel Hill, North Carolina, United States
• Sarah Cannon Research Institute DeptofSarahCannonRes.Inst. (2) — Nashville, Tennessee, United States
• Novartis Investigative Site — Vancouver, British Columbia, Canada
• Novartis Investigative Site — Modena, MO, Italy
• Novartis Investigative Site — Barcelona, Catalonia, Spain
• Novartis Investigative Site — Barcelona, Catalonia, Spain

Full record on ClinicalTrials.gov

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