FPA150 in Patients With Advanced Solid Tumors

This is a Phase 1a/1b open-label, multicenter study to evaluate the dosing, safety,
tolerability, PK, pharmacodynamics, and preliminary efficacy of FPA150 as monotherapy and in
combination with pembrolizumab, an anti-PD1 antibody, in patients with advanced solid tumors.

This study includes a Phase 1a FPA150 Monotherapy Dose Escalation, Phase 1a Monotherapy Dose
Exploration, Phase 1a combination Safety Lead-in (FPA150 + pembrolizumab), a Phase 1b FPA150
Monotherapy Dose Expansion, and a Phase 1b combination Dose Expansion (FPA150 +
pembrolizumab).

The Phase 1a Monotherapy Dose Escalation will include an initial accelerated titration design
followed by a standard 3+3 dose escalation design until the MTD and/or RD for Phase 1b is
determined. The Phase 1a combination Safety Lead-In will start enrolling once the FPA150
monotherapy RD is identified in Phase 1a monotherapy dose escalation and will continue until
the FPA150 MTD/RD in combination is identified. Phase 1a FPA150 monotherapy Dose Exploration
may include cohorts that may enroll beyond 3 patients whose tumors express high levels of
B7-H4 protein and/or have varying levels of B7H4 expression including low (<10% IHC 2+ or 3+
scores) or no expression on their tumor cells (up to 20 additional patients across all dose
levels) to further evaluate safety, PK, pharmacodynamics, and clinical activity at that dose
(to be conditional upon the dose level clearing DLT criteria).

Phase 1b will be the Dose Expansion (monotherapy and combination) portion of the study.

Enrollment into Phase 1b Dose Expansion will begin after identification of the MTD and/or RD
in Phase 1a (monotherapy and Safety Lead-in). Preliminary efficacy will be evaluated in Phase
1b in planned expansion cohorts that include patients with specific tumor types that are
B7-H4+ advanced solid tumors.

Inclusion Criteria (Phase 1a Monotherapy and Combination Therapy):

- Histologically confirmed solid tumors except primary central nervous system (CNS)
tumors.

- Disease that is unresectable, locally advanced, or metastatic.

- Patients must have had progressive disease during or after, or refused, appropriate
standard therapy for their tumor type.

- All patients must have at least one measurable lesion at baseline according to RECIST
v1.1; tumor sites situated in a previously irradiated area, or in an area subjected to
other loco-regional therapy, are not considered measurable unless there has been
demonstrated progression in the lesion.

- Adequate washout for prior anti-cancer therapy (ie, ≥ 5 half-lives or 4 weeks since
the last dose, whichever is shorter).

- Availability of archival tumor tissue and consent to providing archival tumor for
retrospective biomarker analysis, or willingness to undergo a fresh tumor biopsy
during screening (a biopsy is required for patients in the Phase 1a Dose Exploration
portion).

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

- Prior radiotherapy must be completed at least 2 weeks before the first dose of study
drug.

- Prior radiopharmaceuticals (eg strontium, samarium) must be completed at least 8 weeks
before the first dose of study drug.

- Prior surgery requiring general anesthesia must be completed one week before first
study drug administration. Surgery requiring local/epidural must be completed at least
72 hours before first study drug administration.

- Screening laboratory values must meet the following criteria:

- Neutrophils ≥ 1200 cells/ µL

- Platelets ≥ 75 × 103/ µL

- Hemoglobin (Hb) ≥ 9.0 g/dL

- Serum creatinine < 1.5× ULN or creatinine clearance (CrCl) of ≥ 40 mL/ minute

- AST and ALT < 3× ULN (<5ULN in patients with liver metastases)

- Bilirubin < 1.5× ULN (except patients with Gilbert's syndrome, who must have
total bilirubin < 3 mg/dL)

- For Phase 1a Combination Safety Lead-in Patients ONLY:

- B7-H4 positive ovarian cancer

- or cytologically confirmed diagnosis of recurrent epithelial ovarian, primary
peritoneal, or fallopian tube carcinoma that is refractory to existing
therapy(ies) known to provide clinical benefit

- Progressive disease on or after at least two prior regimens of treatment
including at least one platinum-containing regimen, or unable to tolerate
additional chemotherapy

- No prior therapy with an anti-PD1 or PD-L1-directed agent

Inclusion Criteria (Phase 1b monotherapy and combination):

- All Inclusion Criteria for Phase 1a (Exception: Phase 1a Inclusion Criterion #1).

- Positive for B7-H4 expression in an archival or fresh tumor sample as evaluated by an
accompanying validated central laboratory IHC assay. Archival tissue for patients
enrolled in Cohort 1b1 (Breast Cancer) must be within 24 months prior to
pre-screening.

- History of other malignancy is permitted provided it has been definitively treated
with no evidence of recurrence within the past 2 years (Exception: Definitively
treated non-melanoma skin cancer, lobular cancer in situ, and cervical cancer in situ
within 2 years are permitted). Cohort Specific Phase 1b Criteria (monotherapy and
combination therapy)

Breast Cancer Cohorts:

TNBC:

- Histologically or cytologically confirmed metastatic TNBC

- At least two prior lines of systemic chemotherapy with at least one being administered
in the metastatic setting

HR+ Breast:

- Histologically or cytologically confirmed metastatic HR+ breast carcinoma

- Patients must have received at least two prior lines of hormonal therapy

- Patients must have received at least one prior line of systemic chemotherapy (in the
adjuvant or metastatic setting)

Ovarian Cancer (monotherapy):

- Histologically or cytologically confirmed diagnosis of recurrent epithelial ovarian,
primary peritoneal, or fallopian tube carcinoma that is refractory to existing

- Progressive disease on or after at least two prior regimens of treatment including at
least one platinum-containing regimen, or unable to tolerate additional chemotherapy

Endometrial Cancer:

- Histologically or cytologically confirmed recurrent or persistent endometrial cancer
that is refractory to curative or established treatments

- Progressive disease on or after at least one prior regimen of systemic chemotherapy,
or unable to tolerate systemic chemotherapy

Ovarian Cancer (combination):

Histologically or cytologically confirmed diagnosis of recurrent epithelial ovarian,
primary peritoneal, or fallopian tube carcinoma that is refractory to existing

- Progressive disease on or after at least two prior regimens of treatment including at
least one platinum-containing regimen, or unable to tolerate additional chemotherapy

- No prior therapy with an anti-PD1 or PD-L1-directed agent

Exclusion Criteria:

- Immunosuppressive doses of systemic medications, such as steroids or absorbed topical
steroids (doses > 10 mg/day prednisone or equivalent daily) must be discontinued at
least 2 weeks before the first dose of study drug. Short courses of high dose steroids
or continuous low dose (prednisone < 10 mg/day ) are allowed.

- Decreased cardiac function with New York Heart Association (NYHA) > Class 2 at
screening.

- Uncontrolled or significant heart disorder such as unstable angina.

- QT interval corrected for heart rate (QTc) per institutional guidelines > 450 msec for
males or > 470 msec for females at screening.

- Current unresolved infection or history of chronic, active, clinically significant
infection (viral, bacterial, fungal, or other) which, in the opinion of the
Investigator, would preclude the patient from exposure to a biologic agent or may pose
a risk to patient safety.

- Any uncontrolled medical condition or psychiatric disorder which, in the opinion of
the Investigator, would pose a risk to patient safety or interfere with study
participation or interpretation of individual patient results.

- Active, known, or suspected autoimmune disease. Patients with Type I diabetes
mellitus, hypothyroidism requiring only hormone replacement, skin disorders (such as
vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not
expected to recur in the absence of an external trigger, are permitted to enroll.

- Known history of testing positive for human immunodeficiency virus (HIV) 1 or 2 or
known acquired immunodeficiency syndrome (AIDS).

- Positive test for hepatitis B virus surface antigen (HBsAg) or detectable hepatitis C
virus ribonucleic acid (HCV RNA) indicating acute or chronic infection.

- Ongoing adverse effects from prior treatment > Grade 1 (with the exception of Grade 2
alopecia or peripheral neuropathy) based on National Cancer Institute (NCI) Common
Terminology Criteria for Adverse Events (CTCAE).

- Symptomatic interstitial lung disease or inflammatory pneumonitis.

- Untreated or active CNS or leptomeningeal metastases. Patients are eligible if
metastases have been treated and patients are neurologically returned to baseline or
neurologically stable (except for residual signs or symptoms related to the CNS
treatment) for at least 2 weeks before the first dose of study drug.

- Evidence of coagulopathy or bleeding diathesis. Patients receiving stable therapeutic
doses of anti-coagulants will be permitted.

- Transfusion of blood or platelets completed within 72 hours before the first dose of
study drug.

- Any uncontrolled inflammatory GI disease including Crohn's Disease and ulcerative
colitis

- For Cohort 1b1 only: Patients with HER2 positive disease