Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT01957735 : BP31510 (Ubidecarenone,USP) Nanosuspension for Intravenous Injection to Patients With Solid Tumors
PhasePhase 1
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

- The patient has a histologically confirmed solid tumor that is metastatic or
unresectable for which standard measures do not exist or are no longer effective.
(Patients with primary brain cancer or lymphoma are permitted. Patients with brain
metastases are allowed if whole brain radiation was performed and is documented
stable for ? 6 weeks)

- The patient is at least 18 years old.

- The patient has an Eastern Cooperative Oncology Group (ECOG) performance status ? 2

- The patient has a life expectancy of > 3 months.

- Sexually active patients and their partners agree to use an accepted method of
contraception during the course of the study

- Female patients of childbearing potential must have a negative pregnancy test within
1 week prior to beginning study treatment.

- The patient has adequate organ and marrow function as follows:

- ANC ? 1500 mm3, platelets ? 100,000/mm3, hemoglobin ? 9 g/dL,

- serum creatinine ?1.8 mg/dL or creatinine clearance > 50 mL/min (Appendix I);

- bilirubin ? 1.5 mg/dL; alanine aminotransferase (ALT), aspartate transaminase (AST) ?
2.5 times the upper limit of normal if no liver involvement or ? 5 times the upper
limit of normal with liver involvement.

- The patient has serum electrolytes (including calcium, magnesium, phosphorous, sodium
and potassium) within normal limits (supplementation to maintain normal electrolytes
is allowed).

- The patient has adequate coagulation: prothrombin time (PT), partial thromboplastin
time (PTT), and an International Normalized Ratio within normal limits.

- The patient is capable of understanding and complying with the protocol and has
signed the informed consent document.

Exclusion Criteria:

- The patient has uncontrolled intercurrent illness including, but not limited to
uncontrolled infection, symptomatic congestive heart failure (NYHA class III and IV),
uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would
limit compliance with study requirements

- The patient has active heart disease including myocardial infarction within previous
3 months, symptomatic coronary artery disease, arrhythmias not controlled by
medication, unstable angina pectoris, or uncontrolled congestive heart failure (NYHA
class III and IV)

- The patient has received chemotherapy or radiotherapy within 4 weeks or has received
nitrosoureas or mitomycin C within 6 weeks prior to the first dose of study drug.

- The patient has received radiation to ? 25% of his or her bone marrow within 4 weeks
of the first dose of study drug.

- The patient has received an investigational drug within 30 days of the first dose of
study drug.

- The patient has not recovered to grade ? 1 adverse events (AEs) due to
investigational drugs or other medications, administered more than 2 weeks prior to
the first dose of study drug, with the exception of neurotoxicity attributed to
oxaliplatin or taxanes, which must have recovered to < 2 prior to study initiation.

- The patient is pregnant or lactating.

- The patient is known to be positive for the human immunodeficiency virus (HIV). The
effect of BPM31510 on HIV medications is unknown. Note: HIV testing is not required
for eligibility, but if performed previously and was positive, the patient is
ineligible for the study.

- The patient has an inability or unwillingness to abide by the study protocol or
cooperate fully with the investigator or designee.

- The patient is receiving digoxin, digitoxin, lanatoside C or any type of digitalis
alkaloids.

- The patient is receiving colony stimulating factors (CSFs) that cannot be held during
the monitoring period for dose-limiting toxicities (DLT).

- The patient has uncontrolled or severe coagulopathies or a history of clinically
significant bleeding within the past 6 months, such as hemoptysis, epistaxis,
hematochezia, hematuria, or gastrointestinal bleeding.

- The patient has a known predisposition for bleeding such as von Willebrand's disease
or other such condition.

- The patient requires therapeutic doses of any anticoagulant, including LMWH.
Concomitant use of warfarin, even at prophylactic doses, is prohibited.
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT01957735      |      Link to official Clinicaltrials.gov listing
Locations



Home | Brain Tumor Guide | FAQs | Find A Treatment
Noteworthy Treatments | News | Virtual Trial | Videos | Novocure Optune® | Newsletter
Donations | Brain Tumor Centers | Survivor Stories | Temodar®
Fundraising For Research | Unsubscribe | Contact Us

Copyright (c) 1993 - 2019 by:
The Musella Foundation For Brain Tumor Research & Information, Inc
1100 Peninsula Blvd
Hewlett, NY 11557
888-295-4740