Ruxolitinib in Estrogen Receptor Positive Breast Cancer

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
Abramson Cancer Center at Penn Medicine
Study ID
NCT01594216
Phase
PHASE2
Status
Completed

Conditions

  • Estrogen-receptor Positive Invasive Metastatic Breast Cancer

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

This is a Phase II investigator-Initiated trial of the Investigational Drug, Ruxolitinib, in combination with Exemestane in patients with estrogen-receptor positive advanced breast cancer. The objective of this study is to determine the preliminary safety and efficacy of the combination of exemestane and Ruxolitinib (INCB018424).

Key Dates

Start date
Apr 30, 2012
Status verified
May 2024
Primary completion
Apr 30, 2016
Completion
Apr 9, 2016

Study Design

Enrollment
25 participants (actual)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: First Stage
    Ruxolitinib at 25 mg orally, twice daily and Exemestane, 25 mg orally once daily
  • Experimental: Second Stage
    Ruxolitinib at 15 mg orally, twice daily and Exemestane, 25 mg orally once daily

Primary Outcome Measure

Number of Participants With Adverse Events [ Time Frame: 3 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
Abramson Cancer Center of the University of PennsylvaniaPhiladelphiaPennsylvania10104-

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