Phase 1 Safety Study of ACT-PFK-158, 2HCl in Patients With Advanced Solid Malignancies

Inclusion Criteria:

1. Histological or cytological evidence of solid malignancy.

2. Patients must have:

- a. Have advanced solid tumors that are refractory to established therapies known
to provide clinical benefit for the malignancy in question, OR

- b. Be intolerant of established therapies known to provide clinical benefit for
the malignancy in question

3. Patients enrolled in the dose-expansion part of the trial must have at least one
lesion that may qualify as a target lesion based on the RECIST 1.1 criteria.

4. Patient is ambulatory with an ECOG performance status of 0, 1 or 2 and an estimated
life expectancy of > 3 months.

5. Patient is 18 years and older.

6. Patients or their legal representatives must have the ability to read, understand and
provide written informed consent for the initiation of any study related procedures.

7. Patients must have adequate bone marrow reserve as evidenced by:

- a. WBC > 3,000/µL

- b. Absolute neutrophil count (ANC) ≥ 1,500/µL

- c. Platelet count ≥ 100,000/µL

- d. Hemoglobin ≥ 9 gm/dL.

8. Patients must have adequate renal function as evidenced by a serum creatinine ≤ 1.5 X
ULN for the reference laboratory OR a calculated creatinine clearance of ≥ 60 mL/min
by the Cockroft-Gault equation.

9. Patients must have adequate hepatic function as evidenced by AST and ALT values ≤ 3 X
ULN (≤ 5 X ULN if the liver is known to be involved by metastatic disease) and serum
total bilirubin values of ≤ 1.5 X ULN for the reference laboratory.

10. Patients must have INR and PTT values ≤ 1.5X ULN for the reference laboratory.

11. Patients must be recovered from the effects of any prior chemotherapy, radiotherapy
or surgery (i.e., toxicity no worse than Grade 1); for patients who have been on
monoclonal antibody therapy, at least one half-life or 4 weeks (whichever is shorter)
should have elapsed prior to the first scheduled day of dosing with PFK-158.

12. Patients on prior investigational agents must wait at least 5 half-lives before
enrollment into the trial, or 4 weeks if the half-life of the investigational agent
is not known.

13. Female patients of childbearing potential must have a negative pregnancy test within
7 days of the start of treatment.

14. Women of childbearing potential and men with female sexual partners of childbearing
potential must agree to use an effective method of contraception (e.g., oral
contraceptives, double-barrier methods such as a condom and a diaphragm, intrauterine
device) during the study and for 90 days following the last dose of study medication
or to abstain from sexual intercourse for this time; a woman not of childbearing
potential is one who has undergone bilateral oophorectomies or who is
post-menopausal, defined as no menstrual periods for 12 consecutive months.

Exclusion Criteria:

1. Patients with an active infection or with a fever ≥ 38.5°C within 3 days of the first
scheduled day of dosing.

2. Patients with primary CNS tumors as well as patients with CNS metastases are
excluded.

3. Patients with known hypersensitivity to any of the components of PFK-158.

4. Patients who are receiving investigational therapies or who have been treated with
investigational therapies or investigational devices within 5 half-lives of the
investigational therapy or 4 weeks of first scheduled day of dosing with PFK-158 if
the half-live of the investigational agent is not known.

5. Uncontrolled hypertension as defined by SBP > 160 mm/Hg or DBP > 100 mm/Hg despite
medical therapy.

6. Subjects with diabetes.

7. Patients who require pharmacologic doses of corticosteroids; replacement, topical,
ophthalmologic and inhalational steroids are permitted.

8. Patients who require coumadin administration.

9. Patients with mean QTcF values of > 470 msec (in females) or > 450 msec (in males)
following 3 ECGs conducted 5 minutes apart from each other; patients who are known to
have congenital prolonged QT syndromes; or patients who are on medications known to
cause prolonged QT intervals on ECG.

10. Patients with clinically significant cardiovascular co-morbidities including:
congestive heart failure (New York Heart Association class III-IV heart disease),
unstable angina pectoris, cardiac arrhythmias requiring medication or a pacemaker;
myocardial infarction within the past six months; stroke within the past 6 months; or
hypertension requiring more than 2 medications for blood pressure control.

11. Patients with any other concurrent uncontrolled illness, including mental illness or
substance abuse, which may interfere with the ability of the patient to cooperate and
participate in the trial; other examples of such conditions would include COPD or
diabetes mellitus that has required 2 or more hospitalizations in the last year;
severe peripheral vascular disease; poorly controlled auto-immune conditions; recent
serious trauma.

12. Grade 2 or higher peripheral neuropathy.

13. Patients currently known to be positive for, HIV, hepatitis B or C.

14. Patients who are pregnant or lactating.

15. Concurrent or recent (within 1 month) use of thrombolytic agents, or full-dose
anticoagulants (except to maintain patency of preexisting, permanent indwelling IV
catheters). Of note, therapy with low-molecular weight heparin is acceptable as long
as the INR < 2.0.

16. Significant traumatic injury within the past 4 weeks.

17. Patients who are in-patients.