A Study of NKTR-214 in Combination With Nivolumab in Patients With Metastatic and/or Locally Advanced Sarcoma

Inclusion Criteria:

- Male or female age ≥ 12 years at the time of informed consent

- Be capable, willing, and able to provide written informed consent/assent. For patients
< 18 years of age, their parents or legal guardians must sign a written informed
consent. Assent, when appropriate, will be obtained according to institutional
guidelines.

- Be willing to comply with clinical trial instructions and requirements.

- Patients ≥ 18 years must be willing to comply with the mandatory biopsies.

- Patients must have a histologically confirmed metastatic and/or locally advanced
sarcoma by the enrolling institution.

- For histological specific cohorts, patients must have confirmed metastatic and/or
locally advanced osteosarcoma, chondrosarcoma, undifferentiated pleomorphic
sarcoma/malignant fibrous histiocytoma high grade myxofibrosarcoma, vascular sarcoma,
alveolar soft part sarcoma (ASPS), dedifferentiated/pleomorphic liposarcoma, Small
Blue Round CellSynovial, or leiomyosarcoma (LMS) by the enrolling institution.

- Adequate performance status:

- Participants ≥16 years ECOG 0 or 1/KPS 100-70%

- Participants <12-15 years Lanksky 100-70%

- Patients must have at least one prior line of systemic therapy (e.g.chemotherapy,
immunotherapy, targeted or biological therapy) for their sarcoma if standard treatment
is appropriate. Treatment naïve patients may be enrolled if they have refused standard
systemic treatment. Prior adjuvant therapy will not count provided it was completed
more than 6 months previously.

- Presence of measureable disease per RECIST v1.1.Target lesions must not be chosen from
a previously irradiated field unless there has been radiographically and/or
pathologically documented tumor progression in that lesion prior to enrollment.

- On echocardiogram, documented left ventricular ejection fraction >45%. Patients may
instead have a multigated acquisition (MUGA) scan instead of transthoracic
echocardiogram (TTE).

- Adequate organ function

- Women of childbearing potential (WOCBP) † must have a negative urine or serum
pregnancy test at screening and ≤ 72 hours prior to day 1 of study treatment. If the
urine pregnancy test is positive or cannot be confirmed as negative, a serum pregnancy
test will be required.

† A woman of childbearing potential is a sexually mature female who: has not undergone
a hysterectomy or bilateral oophorectomy; or has not been naturally postmenopausal for
at least 24 consecutive months (i.e. has had menses at any time in the preceding 24
consecutive months).

- Male patients with WOCBP partners and female patients of childbearing potential must
be willing to use an adequate method of contraception as outlined in Section 11.9, for
the course of the study through 7 months (male participants) or 5 months (female
participants) after the last dose of study medication.

Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception
for the patient.

- Hematological

- Absolute neutrophil count (ANC) ≥1,500 /mcL

- Platelets ≥100,000 / mcL

- Hemoglobin ≥9 g/dL or ≥5.6 mmol/L

- Renal

- Serum creatinine OR Measured or calculateda creatinine clearance ≤1.5 X upper
limit of normal (ULN) OR ≥60 mL/min for patient with creatinine levels > 1.5 X
institutional ULN (GFR can also be used in place of creatinine or CrCl) Hepatic

- Serum total bilirubin ≤ 1.5 X ULN OR Direct bilirubin ≤ ULN for patients with
total bilirubin levels > 1.5 ULN

- AST (SGOT) and ALT (SGPT) ≤ 2.5 X ULN OR ≤ 5 X ULN for patients with liver
metastases

- Albumin ≥ 2.5 mg/dL Coagulation

- International Normalized Ratio [34] or Prothrombin Time [35]≤1.5 X ULN unless
patient is receiving anticoagulant therapy as long as PT or PTT is within
therapeutic range of intended use of anticoagulants

- Activated Partial Thromboplastin Time (aPTT) ≤1.5 X ULN unless patient is
receiving anticoagulant therapy as long as PT or PTT is within therapeutic range
of intended use of anticoagulants aCreatinine clearance should be calculated per
institutional standard.

Exclusion Criteria:

- History of unstable or deteriorating cardiac disease within the previous 6 months
prior to screening including but not limited to the following:

- Unstable angina or myocardial infarction.

- Congestive heart failure (New York Heart Association [NYHA] Class III or IV).

- Uncontrolled clinically significant arrhythmias.

- Evidence of clinically significant interstitial lung disease or has known history of,
or any evidence of active, non-infectious pneumonitis. .

- Has known active central nervous system (CNS) metastases and/or carcinomatous
meningitis. Patients with previously treated brain metastases may participate
provided:

- No current brain metastasis lesion greated than 2 cm. Patients with prior
metastasis lesions greater than 2 cm that have been removed by surgical and/or
radiotherapy may be enrolled if the lesion has been stable since surgery or
radiotherapy.

- No new or progressing brain metastatis of any size

- No stereotactic radiation or craniotomy within 4 weeks of Cycle 1 Day 1

- They are stable (without evidence of progression by imaging for at least four
weeks prior to the first dose of trial treatment

- No clinically signifigant symptoms secondary to brain metastases(This exception
does not include carcinomatous meningitis which is excluded regardless of
clinical stability.)

- Evidence of clinically significant immunosuppression such as the following:

- Primary immunodeficiency state such as Severe Combined Immunodeficiency Disease

- Concurrent opportunistic infection

- Receiving systemic immunosuppressive therapy (> 2 weeks) including oral steroid
doses > 10 mg/day of prednisone or equivalent within 2 months prior to
enrollment. (Steroids for pre-medication for imaging studies are allowed.)

- History or evidence of symptomatic autoimmune disease (e.g., pneumonitis,
glomerulonephritis, vasculitis, or other), or history of active autoimmune disease
that has required systemic treatment (i.e., use of corticosteroids, immunosuppressive
drugs or biological agents used for treatment of autoimmune diseases) in past 2 years
prior to enrollment. Replacement therapy (e.g., thyroxine for hypothyroidism, insulin
for diabetes or physiologic corticosteroid replacement therapy for adrenal or
pituitary insufficiency) is not considered a form of systemic treatment for autoimmune
disease.

- Known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies) disease

- Patients known to be positive for active Hepatitis B (HBsAg reactive), or Hepatitis C
(HCV RNA (qualitative) is detected)

- Prolonged QTcF > 450 ms for men and > 470 ms for women at Screening.

- Patients who have received a live vaccine within 30 days of the start date of the
planned study therapy. Note: Seasonal influenza vaccines for injection are generally
inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g.,
Flu-Mist®) are live attenuated vaccines, and are not allowed.

- Has a known history of active TB (Bacillus Tuberculosis)

- Is currently participating and receiving study therapy or has participated in a study
of an investigational agent and received study therapy or used an investigational
device within 4 weeks of the first dose of treatment.

- Has a known history of active TB (Bacillus Tuberculosis)

- Is currently participating and receiving study therapy or using an investigational
device or has participated in a study of an investigational agent and received study
therapy or used an investigational device within 4 weeks of the first dose of
treatment.

- Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events
due to agents administered more than 4 weeks earlier.

- Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy
within 3 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at
baseline) from adverse events due to a previously administered agent.

- Note: Patients with ≤ Grade 2 neuropathy are an exception to this criterion and
may qualify for the study.

- Note: If patient received major surgery, they must have recovered adequately from
the toxicity and/or complications from the intervention prior to starting
therapies.

- Hypersensitivity to nivolumab or any of its excipients.

- Hypersensitivity to NKTR-214 or any of its excipients.

- Need for > 2 antihypertensive medications for management of hypertension (including
diuretics).

- Women who are pregnant or breast feeding