Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)

The myeloproliferative neoplasms (MPN), most notably polycythemia vera (PV), essential
thrombocythemia (ET), and primary myelofibrosis (PMF) are a diverse but inter-related suite
of clonal disorders of pluripotent hematopoietic stem cells (Tefferi et al., 2008). The MPN
share a range of biological, pathological, and clinical features including the relative
overproduction of one or more cells of myeloid origin, growth factor independent colony
formation in vitro, marrow hypercellularity, extramedullary hematopoiesis, splenomegaly and
hepatomegaly, and thrombotic and/or hemorrhagic diatheses (Tefferi et al., 2005).

This is an open-label, non-randomized, dose-escalation study, to be conducted in two phases:
a single-centre dose-escalation phase with supernumerary patient addition (Part 1), to
determine the safety and tolerability of CYT387, and to identify a therapeutic dose for the
confirmation portion of the study; and a multiple-centre dose-confirmation phase (Part 2),
which will be a cohort expansion at or below the maximum tolerated dose (MTD) of CYT387.

In Part 1 of the study, patients will be assigned to dose levels in successive cohorts
starting with a dose in the first cohort of 100 mg/day, administered orally as a single daily
dose (ie QD: at least 20 and no more than 28 hours apart, preferably in a fasted state at
least one hour before and two hours after a meal). Dose-escalation will proceed initially
with a 1.5-fold increment however, based on toxicity and efficacy information at a specific
dose level, the dose escalation increment may be reduced to a 1.25-fold escalation at the
discretion of the investigator. At any dose level, if one patient experiences a Grade 2
toxicity or higher, the dose-escalation may only proceed with 1.25-fold increments.

The MTD is defined as the highest dose level at which > 2 of 6 subjects develop first cycle
DLT. New dose levels may begin accrual only if all subjects at the current dose level have
been observed for a minimum of 28 days from the first day of treatment. The recommended Phase
II dose will be the MTD unless significant clinical activity (efficacy) is seen below the
MTD. With the exception of the first cohort, dose levels may be decreased from the intended
dose levels for the next cohort, if Grade 2 or greater toxicities are observed.

Twenty (20) patients will be assigned to receive CYT387 at 150 mg twice daily (BID) with
doses approximately 10-12 hours apart to determine the comparative safety, tolerability and
preliminary activity of CYT387 administered twice-daily. Initially, a maximum of 6 (six)
patients will be enrolled for safety assessment. If none of the six patients experiences a
first-cycle DLT, then the remaining 14 patients may be enrolled following approval by the
Data Safety Monitoring Board (DSMB).

In the multi-centre portion of the study (Part 2), sixty (60) additional patients will be
dosed at either 150 mg or 300 mg once daily (QD). Subjects will be evaluated weekly for the
first cycle, every 2 weeks for cycle 2, and at the end of each subsequent cycle for up to 9
cycles of CYT387 treatment. If, after 6 months of therapy an individual patient has not
experienced a drug-related serious adverse event (SAE), the investigator may, with the
written concurrence of the independent safety monitor, elect to have that patient's monthly
safety assessment performed by a registered medical practitioner remote to the
investigational centre. Subjects will return for a follow-up visit 30 days after completion
of the last dose of study drug. Subjects who achieve at least stable disease or better and
tolerate the drug well may be allowed to continue to receive CYT387 beyond the planned 9
cycles under the extension protocol CCL09101E.

Inclusion Criteria:

- Diagnosis of PMF or post-polycythemia Vera (PV) or post-essential Thrombocythemia (ET)
MF as per revised World Health Organization (WHO) criteria.

- High-risk or Intermediate-2 risk MF (as defined by the International Prognostic
Scoring System [IPSS]; Appendix 13.6); or intermediate-I risk MF (IPSS) associated
with symptomatic splenomegaly/hepatomegaly and/or unresponsive to available therapy.

- Must be at least 18 years of age with life expectancy of ≥ 12 weeks.

- Must be able to provide informed consent and be willing to sign an informed consent
form.

- Must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or
2.

- Must have evidence of acceptable organ function within 7 days of initiating study drug
as evidenced by the following:

- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≤ 2.5 x upper
limit of normal (ULN) (or ≤ 5 x ULN if in the investigator's opinion the
elevation is due to extramedullary hematopoiesis)

- Bilirubin ≤ 2.0 x ULN or direct bilirubin < 1.0

- Serum creatinine ≤ 2.5 x ULN

- Absolute neutrophil count ≥ 500/µL

- Platelet count ≥ 50,000/µL

- Females of childbearing potential must have a negative pregnancy test within 4 days of
initiating study drug.

Exclusion Criteria:

- Any chemotherapy (eg, hydroxyurea), immunomodulatory drug therapy (eg, thalidomide),
immunosuppressive therapy, corticosteroids > 10 mg/day prednisone or equivalent, or
growth factor treatment (eg, erythropoietin) within 14 days prior to initiation of
study drug.

- Incomplete recovery from major surgery within four weeks of study entry.

- Radiation therapy within four weeks of study entry.

- Women of childbearing potential, unless surgically sterile for at least 3 months (ie,
hysterectomy), OR postmenopausal for at least 12 months (FSH > 30 U/mL), OR unless
they agree to take appropriate precautions to avoid pregnancy (with at least 99%
certainty) from screening through end of study. Permitted methods for preventing
pregnancy must be communicated to study subjects and their understanding confirmed.

- Men who partner with a woman of childbearing potential, unless they agree to take
appropriate precautions to avoid pregnancy (with at least 99% certainty) from
screening through to the end of study. Permitted methods for preventing pregnancy must
be communicated to study subjects and their understanding confirmed.

- Females who are pregnant or are currently breastfeeding.

- Known positive status for HIV.

- Clinically active hepatitis B or C.

- Diagnosis of another malignancy unless free of disease for at least three years
following therapy with curative intent. Patients with early-stage basal cell or
squamous cell skin cancer, cervical intraepithelial neoplasia, cervical carcinoma in
situ or superficial bladder cancer may be eligible to participate at the
Investigator's discretion.

- Any acute active infection.

- Cardiac dysrhythmias requiring treatment, or prolongation of the QTc (Fridericia)
interval to > 450 msec for males or > 470 msec for females at prestudy screening,
unless attributable to pre-existing bundle branch block.

- Presence of ≥ Grade 2 peripheral neuropathy.

- Uncontrolled congestive heart failure (New York Heart Association Classification 3 or
4), uncontrolled or unstable angina, myocardial infarction, cerebrovascular accident,
or pulmonary embolism within 3 months prior to initiation of study drug.

- Uncontrolled inter current illness or any concurrent condition that, in the
Investigator's opinion, would jeopardize the safety of the patient or compliance with
the protocol.