Phase I Study of MLN 9708 in Addition to Chemotherapy for the Treatment of Acute Lymphoblatic Leukemia in Older Adults

This research study is evaluating a combination of drugs considered standard treatment
for children and young adults with acute lymphoblastic leukemia (ALL), in combination
with a new drug called MLN 9708. Additionally, the study is also evaluating if bone
marrow or stem cell transplantation, which will be given to some participants, helps to
prevent ALL from returning.

Inclusion Criteria:

- Acute lymphoblastic leukemia, excluding known mature B-cell ALL by the presence of
any of the following: surface immunoglobulin, L3 morphology, t(8;14)(q24;q32),
t(8;22), or t(2;8).

- Patients with mature B-cell ALL will be removed from the protocol as soon as that
diagnosis is made and should be treated on a B-cell leukemia (Burkitt's) protocol.
NOTE: Patients with T-cell surface markers and a t(8;14)(q24;q11) remain eligible.

- Patients with lymphoblastic lymphoma are also eligible

- No prior anti-leukemic therapy except the following are allowed: <1 week of
corticosteroids, or hydroxyurea or emergent leukopheresis. Longer steroid use for
diseases other than leukemia is permitted.

- Age 51- 75 years

- Voluntary written consent must be given before performance of any study-related
procedures not part of standard medical care, with the understanding that consent
may be withdrawn by the patient at any time without prejudice to future medical
care.

- If patient is known to be HIV positive, they will not be eligible for the protocol.
HIV testing is not mandatory prior to protocol enrollment.

- Patients whose comorbid medical condition, in the investigator's opinion, would make
participation in this trial and adherence to the protocol guidelines difficult
should be excluded.

- Patients with an active psychiatric or mental illness making informed consent or
careful clinical follow-up unlikely are excluded.

- Ejection fraction ≥ 45%

- Creatinine<2.0 times upper limit of normal

- Total bilirubin < 1.5 times upper limit of normal except for known conjugation
diseases such as Gilbert's, ALT and AST <3.0 times upper limit of normal. Direct
bilirubin is not an inclusion criteria.

- ECOG performance status of 0, 1, 2

- Non pregnant and non lactating Female patients who:

- Are postmenopausal for at least 1 year before the screening visit, OR

- Are surgically sterile, OR

- If they are of childbearing potential, agree to practice 2 effective methods of
contraception, at the same time, from the time of signing the informed consent
form through 90 days after the last dose of study drug, AND

- Must also adhere to the guidelines of any treatment-specific pregnancy
prevention program, if applicable, OR

- Agree to practice true abstinence when this is in line with the preferred and
usual lifestyle of the subject. (Periodic abstinence [eg, calendar, ovulation,
symptothermal, post-ovulation methods] and withdrawal are not acceptable
methods of contraception.)

- Male patients, even if surgically sterilized (i.e., status post-vasectomy), must
agree to one of the following:

- Agree to practice effective barrier contraception during the entire study
treatment period and through 90 days after the last dose of study drug, OR

- Must also adhere to the guidelines of any treatment-specific pregnancy
prevention program, if applicable, OR

- Agree to practice true abstinence when this is in line with the preferred and
usual lifestyle of the subject. (Periodic abstinence (eg, calendar, ovulation,
symptothermal, post-ovulation methods] and withdrawal are not acceptable
methods of contraception.)

Exclusion Criteria:

- Patients meeting any of the following exclusion criteria are not to be enrolled in
the study.

- Female patients who are lactating or have a positive serum pregnancy test during the
screening period.

- Major surgery within 14 days before enrollment. Biopsies and line placement
procedures are not exclusion criteria.

- Radiotherapy within 14 days before enrollment. Radiotherapy is excluded during
induction and consolidation 1 while receiving MLN 9708.

- Evidence of current uncontrolled cardiovascular conditions, including uncontrolled
hypertension, uncontrolled cardiac arrhythmias, symptomatic congestive heart
failure, unstable angina, or myocardial infarction within the past 6 months.

- Active hepatitis B or C virus infection, or known human immunodeficiency virus (HIV)
positive. Hepatitis and HIV testing are not required prior to the start of
treatment.

- Any serious medical or psychiatric illness that could, in the investigator's
opinion, potentially interfere with the completion of treatment according to this
protocol.

- Known allergy to any of the study medications, their analogues, or excipients in the
various formulations of any agent.

- Patient has ≥ Grade 3 peripheral neuropathy, or Grade 2 with pain on clinical
examination during the screening period.

- Known GI disease or GI procedure that could interfere with the oral absorption or
tolerance of MLN9708 including difficulty swallowing.

- Diagnosed or treated for another malignancy within 2 years before study enrollment
or previously diagnosed with another malignancy and have any evidence of residual
disease. Patients with nonmelanoma skin cancer or carcinoma in situ of any type are
not excluded if they have undergone complete resection.

- Participation in other clinical trials, including those with other investigational
agents not included in this trial, within 21days of the start of this trial and
throughout induction and consolidation 1 portions of this trial (while on MLN 9708).
Patients may enroll in transplant and post transplant studies after consolidation 1
treatment (See Section 6.5).

- Systemic treatment, within 14 days before the first dose of MLN9708, with strong
inhibitors of CYP1A2 (fluvoxamine, enoxacin), strong inhibitors of CYP3A
(clarithromycin, telithromycin, itraconazole, voriconazole, ketoconazole,
nefazodone, posaconazole) or strong CYP3A inducers (rifampin, rifapentine,
rifabutin, carbamazepine, phenytoin, phenobarbital), or use of Ginkgo biloba or St.
John's wort. Ciprofloxocin should not be administered for at least 2 days before MLN
9708 administration. Extended release ciprofloxocin should not be administered for
at least 3 days prior to MLN 9708 administration.