Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Utah
With
Eli Lilly and Company
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
At least 1 bone metastases must be present
Urinary N-telopeptide level above 20nM BCE/mM creatinine measured at ARUP
Archived or freshly biopsied primary and/or bone metastatic tumor tissue available in paraffin-embedded blocks or slides that is expected to yield 9 slides
Life expectancy of ≥ 6 months
Toxicity related to prior treatments must either have resolved to grade 1 or less, returned to baseline, or be deemed irreversible
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 (within 28 days prior to enrollment)
Planning to remain on current breast cancer therapy for at least 12 weeks.
At least one prior line of therapy for metastatic breast cancer
Concurrent treatment with bisphosphonates or denosumab is required.
* Any prior history, or current evidence of second- or third-degree heart block
* Heart rate ˂ 40 beats per minute at screening
* ECG second degree heart block (Mobitz's Type 2 or Wenckebach)
* Complete heart block
* Left bundle branch block or bifascicular block (right bundle branch block and left anterior hemiblock together)
* Episodes of ventricular tachycardia
Any known prior malignancy (not including non-melanoma skin cancers), unless treated with curative intent
A serious uncontrolled medical disorder or active infection, which would impair the ability of the subject to receive protocol therapy
Current or recent (within 3 months) gastrointestinal disease that could impact the absorption (i.e., unmanageable diarrhea or malabsorption at the time of screening)
* Total bilirubin ˃ 1.5 x institutional upper limit of normal (IULN) (Unless due to diagnosis of Gilbert's Syndrome)
* Alanine aminotransaminase (ALT) and aspartate aminotransaminase (AST) ˃ 2.5 x IULN
Inadequate renal function defined as: Serum creatinine ˃ 1.5 x ULN
Prothrombin time (PT)/partial thromboplastin time (PTT) ˃ 1.5 times the ULN
Serum sodium, potassium, and calcium levels not within normal limits.
Any atrophic macular condition including intermediate or advanced age-related macular degeneration
Patients receiving medications that are known to be substrates of CYP2C8 (including paclitaxel), CYP2C9, or CYP2C19 or to be oral substrates of CYP3A with narrow therapeutic window (listed on http://medicine.iupui.edu/clinpharm/ddis/main-table). Subjects who have discontinued any of these medications must have a wash-out period of at least 5 days or 5 half-lives of the drug (whichever is longer) prior to the first dose of merestinib
Exposure to any investigational drug or placebo within 4 weeks of enrollment
Any other sound medical, psychiatric, and/or social reasons as determined by the investigator
History of diseases with influence on bone metabolism, such as Paget's disease, osteogenesis imperfecta, active primary or secondary hyperparathyroidism, and primary or secondary hyperthyroidism within 12 months prior to study entry
Patients with known symptomatic brain metastasis. Subjects with controlled brain metastasis (no radiographic progression at least 4 weeks following radiation and/or surgical treatment and no neurological signs or symptoms) will be allowed
History of allergy to merestinib or chemically related compounds
History of osteonecrosis of the jaw
Change in chemotherapy or hormone therapy within 8 weeks of the start of the study.
Active gout or inflammatory arthritis requiring treatment
Use within 28 days of registration of calcitonin, recombinant parathyroid hormone-related peptides, mithramycin, radium, strontium ranelate, or gallium nitrate.
Adult patients who require monitored anesthesia for PET scanning due to claustrophobia.
Clareo Health | Merestinib on Bone Metastases in Subjects With Breast Cancer
