GS-5829 in Combination With Fulvestrant or Exemestane in Women With Advanced Estrogen Receptor Positive, HER2 Negative-Breast Cancer

Key Inclusion Criteria:

   - Histologically or cytologically confirmed breast cancer with evidence of metastatic or
   locally advanced disease not amenable to resection or radiation therapy with curative
   intent and who have progressed during treatment with at least one prior hormonal
   therapy

      - Phase 1b Dose Escalation - Individuals may have had unlimited prior hormonal
      therapy and a total of 2 prior chemotherapy regimens (adjuvant chemotherapy is
      considered 1 regimen). Individuals may have progressed on fulvestrant or
      exemestane.

      - Randomized Phase 2 Dose Expansion - Individuals may have disease progression
      during treatment or within 12 months of completion of endocrine therapy
      (tamoxifen, and/or AI) in the adjuvant setting, or disease progression during
      treatment with endocrine therapy (tamoxifen, AI or CDK4/6 inhibitor plus AI) for
      advanced/metastatic disease. Individuals may have had unlimited prior hormonal
      therapy, but must be naive to fulvestrant in the metastatic setting. A total of 2
      prior chemotherapies are allowed, however, only one for metastatic disease is
      permitted.

   - Documentation of ER positive (≥ 1% positive stained cells by local standards) based on
   the most recent tumor biopsy, unless bone-only disease

   - Documented HER2-negative tumor based on local testing on most recent tumor biopsy
   (immunohistochemistry score 0/1+ or negative by in situ hybridization HER2/CP17 ratio
   < 2 or for single probe assessment HER2 copy number < 4)

   - Post-, pre- or peri-menopausal women considered to be in the post-menopausal state as
   defined by one of the following:

      - Age ≥ 60 years

      - Age < 60 years and cessation of regular menses for at least 12 consecutive months
      in the absence of chemotherapy, tamoxifen, toremifene, or ovarian suppression and
      serum estradiol and follicle-stimulating hormone (FSH) level within the
      post-menopausal range

      - Prior bilateral oophorectomy

      - Pre-/peri-menopausal women can be enrolled if amenable to be treated with the
      luteinizing-hormone releasing hormone (LHRH) agonist, goserelin. Individuals must
      have commenced treatment with goserelin or an alternative LHRH agonist at least 4
      weeks prior to Cycle 1 Day 1 (C1D1). If individuals have received an alternative
      LHRH agonist prior to study entry, they must switch to goserelin on or before
      Cycle 1 Day 1 (C1D1) for the duration of the study

   - Measurable disease defined per RECIST v. 1.1, or bone-only disease must have a lytic
   or mixed lytic blastic lesion that can be accurately assessed by computed tomography
   (CT) or magnetic resonance imaging (MRI). Individuals with bone-only disease and
   blastic-only metastases are not eligible

   - All acute toxic effects of any prior antitumor therapy resolved to Grade ≤ 1 before
   the start of study drug dosing (with the exception of alopecia [Grade 1 or 2
   permitted] and neurotoxicity [Grade 1 or 2 permitted])

   - Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤ 1

   - Life expectancy of ≥ 3 months, in the opinion of the investigator

   - Adequate organ function defined as follows:

      - Hematologic: Platelets ≥ 100 x 10^9/L; Hemoglobin ≥ 9.0 g/dL; absolute neutrophil
      count (ANC) ≥ 1.5 x 10^9/L (without platelet transfusion or any granulocytic
      growth factors within previous 7 days of the hematologic laboratory values
      obtained at screening visit)

      - Hepatic: aspartate transaminase (AST) / alanine transaminase (ALT) ≤ 2.5 x upper
      limit of normal (ULN) (if liver metastases are present, ≤ 5 x ULN); total or
      conjugated bilirubin ≤ 1.5 x ULN

      - Renal: Serum Creatinine ≤ 1.5 x ULN or creatinine clearance (CrCl) ≥ 60 mL/min as
      calculated by the Cockroft-Gault method

   - Coagulation: International Normalized Ratio (INR) ≤ 1.2

   - Negative serum pregnancy test

   - Females of childbearing potential who engage in heterosexual intercourse must agree to
   use protocol specified method(s) of contraception as described in the study protocol

   - Females who are nursing must agree to discontinue nursing before the first dose of
   GS-5829

   - Able and willing to provide written informed consent to participate in the study

Key Exclusion Criteria:

   - History or evidence of clinically significant disorder, condition, or disease that, in
   the opinion of the investigator or the Gilead medical monitor would pose a risk to
   individual safety or interfere with the study evaluations, procedures, or completion

   - Known brain metastasis or leptomeningeal disease (Note: if treated and stable at least
   6 months prior to enrollment, individual is eligible).

   - Uncontrolled intercurrent illness including, but not limited to, active uncontrolled
   infection, active or chronic bleeding event within 28 days prior to C1D1, uncontrolled
   cardiac arrhythmia, or psychiatric illness/social situation that would limit
   compliance with study requirements as judged by treating physician

   - Myocardial infarction, symptomatic congestive heart failure (New York Heart
   Association Classification > Class II), unstable angina, or serious uncontrolled
   cardiac arrhythmia within the last 6 months of C1D1

   - Major surgery, defined as any surgical procedure that involves general anesthesia and
   a significant incision (i.e., larger than what is required for placement of central
   venous access, percutaneous feeding tube) within 28 days of C1D1

   - Impairment of gastrointestinal (GI) function or GI disease that may significantly
   alter the absorption of GS-5829, including any unresolved nausea, vomiting, or
   diarrhea that is Common Terminology Criteria for Adverse Events (CTCAE) Grade > 1

   - Minor surgical procedure(s) within 7 days of enrollment or randomization, or not yet
   recovered from prior surgery (placement of central venous access device, fine needle
   aspiration, or endoscopic biliary stent ≥ 1 day before enrollment or randomization is
   acceptable)

   - History of a concurrent or second malignancy, except for: adequately treated local
   basal cell or squamous cell carcinoma of the skin; cervical carcinoma in situ;
   superficial bladder cancer; adequately treated Stage 1 or 2 cancer currently in
   complete remission; any other cancer that has been in complete remission for ≥ 5 years

   - Anti-tumor therapy (chemotherapy, chemoradiation, radiation, antibody therapy,
   molecular targeted therapy) within 21 days or 5 half-lives whichever is longer, of
   C1D1 (6 weeks for nitrosoureas, mitomycin C, or molecular agents with t1/2 > 10 days);
   5 half-lives of any investigational drug; concurrent use of goserelin for
   pre-/peri-menopausal breast cancer and exemestane or fulvestrant per the protocol are
   permitted

   - History of long QT syndrome or whose corrected QT interval (QTc) measured (Fridericia
   method) at screening is prolonged (> 470 ms). Individuals who screen fail due to this
   criterion are not eligible to be re-screened

   - Prior exposure to any bromodomain (BET) inhibitors

   - Known hypersensitivity to the study drugs (GS 5829, fulvestrant or exemestane), the
   metabolites, or formulation excipients

   - Immunotherapy within 6 months of C1D1

   - Evidence of bleeding diathesis or clinically significant bleeding, within 28 days of
   C1D1 or history of hemoptysis of > 2.5 mL/1 teaspoon within 6 months of C1D1

   - Anticoagulation/antiplatelet therapy within 7 days of C1D1, including acetylsalicylic
   acid, low molecular weight heparin, or warfarin

   - Known human immunodeficiency virus (HIV) infection

   - Hepatitis B surface Antigen (HBsAg) positive

   - Hepatitis C virus (HCV) antibody positive with HCV RNA positive

   - Use of moderate/strong cytochrome P450 (CYP)3A4 inhibitors or moderate/strong CYP3A4
   inducers within 2 weeks prior to C1D1

   - History of high grade esophageal or gastric varices

Note: Other protocol defined Inclusion/Exclusion criteria may apply.