Determining the Effects of Temozolomide Followed by Nivolumab in Patients With Colorectal Cancer

Inclusion Criteria:

- Subject or legally authorized representative, is willing and able to provide written
informed consent/assent for the trial

- Histologically- or cytologically- confirmed CRC

- Locally advanced or metastatic CRC

- Confirmation of MGMT promoter methylation on archived tissue by PCR analysis (any
time).

- MGMT promoter methylation is determined using the ARUP laboratory assay (or similar).
Total methylation is calculated as an average across listed CpG sites. Total
methylation of 0-9 percent is reported as "Not detected" 10-29 percent as "Low level"
and equal or more than 30 percent as "Detected". Patients will require MGMT promoter
methylation to be "detected" in order to be eligible.

- Undergone testing for MSI/dMMR and determined to be MSS or MMR proficient

- Subjects must be refractory or intolerant to at least 2 lines of standard
chemotherapy, according to NCCN guidelines for patients eligible for intensive
therapy. At a minimum, such therapies should include regimens containing oxaliplatin
or irinotecan in combination with a fluoropyrimidine (e.g., FOLFOX or FOLFIRI or their
variants).

- At least one index lesion which is measurable based on RECIST 1.1

- Be >/= 18 years of age on day of signing informed consent

- Consent for tumor biopsies and blood draws for research purposes

- Have an ECOG performance status of 0 or 1

- Demonstrate adequate organ function as defined in Table 6.1, all screening labs should
be performed within 28 days of treatment initiation.

Adequate Organ Function Laboratory Values

Hematological

- Absolute neutrophil count (ANC) >/= 1,500/mcl

- Platelets >/= 100,000/mcl

- WBC >/= 2000/ul

- Hemoglobin >/= 9.0 g/dL

Renal

- Serum creatinine
- Measured or calculated creatinine clearance (GFR can also be used in place of
creatinine of CrCl) >/= 60 mL/min for subject with creatinine levels > 1.5 x
institutional ULN (Creatinine clearance should be calculated per institutional
standard)

Hepatic

- Serum total bilirubin total bilirubin levels > 1.5 ULN

- AST (SGOT) and ALT (SGPT) metastases

- Female subject of childbearing potential should have a negative serum pregnancy within
2 weeks prior to starting treatment

- Female subjects of childbearing potential should be willing to use 2 methods of birth
control or be surgically sterile, or abstain from heterosexual activity for the course
of the study through 5 months after the last dose of study medication. Subjects of
childbearing potential are those who have not been surgically sterilized or have not
been free from menses for > 1 year

- Male subjects should agree to use an adequate method of contraception starting with
the first dose of study therapy through 7 months after the last dose of study therapy
(defined in section 7.1). In addition, male subjects must be willing to refrain from
sperm donation during this time.

Coagulation

- International Normalized Ratio (INR) or Prothrombin Time (PT) subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic
range of intended use of anticoagulants

- Activated Partial Thromboplastin Time (aPTT) anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use
of anticoagulants

Exclusion Criteria:

- Subject is currently participating in or has participated in a study of an
investigational agent or using an investigational device within 4 weeks of the first
dose of treatment.

- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy (>10
mg/day prednisone, or equivalent) or any other form of immunosuppressive therapy
within 7 days prior to the first dose of trial treatment. inhaled or topical steroids
are permitted in the absence of active autoimmune disease

- Prior chemotherapy, targeted small molecule therapy, or biological therapy, within 2
weeks prior to study Day 1 or who has not recovered (i.e., from adverse events due to a previously administered agent (exc. alopecia)

- If subject received major surgery, they must have recovered adequately prior to
starting therapy

- Has a known additional malignancy that is progressing or requires active treatment.
Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the
skin, or in situ cervical cancer that has undergone potentially curative therapy

- Has known active central nervous system (CNS) metastases and/or carcinomatous
meningitis. Subjects with previously treated brain metastases may participate provided
they are stable (without evidence of progression by imaging for at least four weeks
prior to the first dose of trial treatment any neurologic symptoms have returned to
baseline), have no evidence of new or enlarging brain metastases, and are not using
steroids for at least 7 days prior to trial treatment,

- Has an active, known or suspected autoimmune disease requiring systemic treatment
within the past 3 months or a documented history of clinically severe autoimmune
disease, or a syndrome that requires systemic steroids or immunosuppressive agents.
Subjects with vitiligo or resolved childhood asthma/atopy, type 1 diabetes mellitus
are permitted. Subjects that require intermittent use of bronchodilators or local
steroid injections would not be excluded from the study. Subjects with hypothyroidism
stable on hormone replacement or Sjorgen's syndrome will not be excluded from the
study.

- Has evidence of known interstitial lung disease or active, non-infectious pneumonitis

- Has an active infection requiring systemic therapy

- Has a history or current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the trial, interfere with the subject's
participation for the full duration of the trial, or it is not in the best interest of
the subject to participate, in the opinion of the treating investigator

- Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial

- Is pregnant or breastfeeding, or expecting to conceive or father children within the
projected duration of the trial, starting with the pre-screening or screening visit
through 5 months for females, 7 months for males after the last dose of trial
treatment

- Prior anti-PD-1, anti-PDL-1, anti-PDL-2, anti-Cytotixic T-lymphocyte-associated
antigen-4 (CTLA-4) antibody or any other antibody or drug specifically targeting
T-cell co-stimulation or checkpoint pathways

- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies)

- Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA
[qualitative] is detected)

- Has received a live vaccine within 30 days prior to the first dose of trial treatment

- Subjects is a prisoners or compulsory detained