BP31510 (Ubidecarenone,USP) Nanosuspension for Intravenous Injection to Patients With Solid Tumors

This is a Phase 1a/b multicenter, open-label, non-randomized, dose-escalation study to
examine the dose limiting toxicities (DLT) of BPM31510 administered as a 144-hour continuous
intravenous (IV) infusion as monotherapy(treatment Arm 1)and in combination with chemotherapy
(treatment Arm 2) in patients with solid tumors.In the Phase 1a portion of the trial,
patients who meet eligibility parameters will receive 2 consecutive 72-hour infusions of
BPM31510 twice weekly on Tuesday and Friday (i.e., Days 1, 4, 8, 11, 18, 22 and 25),
essentially receiving BPM31510 treatment for 144 hours per week of each 28-day cycle. At each
dose level of Arm 1 and Arm 2, patients will be treated for either 8 hours at minimum of
outpatient monitoring or inpatient monitoring for the first 24-hrs of the first infusion of
Cycle 1.All other treatments will be administered in an outpatient setting.Dose limiting
toxicities will be assessed during Cycle 1.

The study is a standard 3 + 3 dose escalation design with the dose escalated in successive
cohorts of 3 to 6 patients each.Toxicity at each dose level will be graded according to
National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE v4.02).
Safety oversight will be provided by the Cohort Review Committee (CRC).The CRC will review
and confirm all DLTs and will continue to monitor safety throughout the study (including Arm
2).

Assessments of the antitumor activity of BPM31510 will be performed at the end of Cycle 2 and
every 2 cycles thereafter using standard techniques such as computerized tomography (CT) or
magnetic resonance imaging (MRI) for patients with measurable disease.Response will be
evaluated using Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 .Patients who
experience no unacceptable toxicity or disease progression, may receive additional 28-day
cycles for up to 1 year on Arm 1 or 2. Patients on Arm 1 who progress may elect to continue
BPM31510 treatment in combination with gemcitabine, 5-FU, or docetaxel at the treating
physician's discretion. Once a dose level of BPM31510 monotherapy is evaluated and the CRC
determines it safe to escalate to the next dose level, Cohort 1 of Treatment Arm 2 of
BPM31510 in combination with chemotherapy will open to accrual. Cohort 1 of Arm 2 patients
will be enrolled onto one of 3 chemotherapies, gemcitabine, 5-FU, or docetaxel. Cycle 1 of
combination therapy (Arm 2) is 6 weeks in duration for patients with BPM31510 administered
twice weekly on Tuesday and Friday for 6 weeks and chemotherapy administered on Mondays, Days
21, 28 and 35. Cycles 2-12 are 4 weeks in duration with BPM31510 administered twice weekly on
Tuesday and Friday for 4 weeks and chemotherapy administered on Mondays, Days 7, 14 and 21.
Dose limiting toxicities will be assessed during Cycle 1. Response will be assessed after
Cycle 2 (10 weeks) and responders who continue onto Cycles 2-12 will be assessed every 2
cycles (8 weeks). Patients who progress and crossover to Arm 2 will be reconsented and must
meet eligibility before restarting BPM31510. Crossover patients are not evaluated for DLTs on
Arm 2 and all cycles of combination therapy are 4 weeks in duration (Cycles 1-12). BPM31510
is administered twice weekly on Tuesdays and Fridays for 4 weeks and chemotherapy
administered on Mondays, Days 7, 14 and 21 for all crossover patients on Arm 2. Patients will
continue BPM31510 in combination with chemotherapy for a maximum of 12 cycles in the absence
of intolerable toxicity and progression. Patients on Arm 2 who progress on one type of
chemotherapy may not switch to one of the other chemotherapy agents in combination with
BPM31510.However, if the chemotherapy component (ie, 5-FU, gemcitabine, or docetaxel) of
combination therapy is discontinued due to chemotherapy-related toxicity, patients may
continue to receive BPM31510 as monotherapy.

Once the maximum tolerated dose (MTD) of BPM31510 as monotherapy and in combination with
chemotherapy are established, an expansion cohort will be enrolled (a total of 12-15 patients
for monotherapy and a total of 10 patients for each combination therapy).

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.