A Phase 2 Study of ZEN003694 in Combination with Talazoparib in Patients with Triple-Negative Breast Cancer

This is a two-part open label, non-randomized, Phase 2, study of ZEN003694 in combination
with Talazoparib in patients with TNBC without germline mutations of BRCA1 or BRCA2. Part 1
is a dose escalation and Part 2 is a Simon 2-Stage design. There are 3 expansion cohorts:
Expansion Cohort A (combination treatment in post-TROP2-ADC patients), Expansion Cohort B
(ZEN003694 monotherapy), and Expansion Cohort C (combination treatment in TROP2-ADC-naive
patients).

Inclusion Criteria:

1. Females or males age ≥ 18 years (at time of signing informed consent)

2. Parts 1 and 2 only: Histologically confirmed metastatic or recurrent or locally
advanced triple-negative breast cancer (estrogen receptor (ER) ≤10%; progesterone
receptor (PR) ≤10%; and HER2 negative by immunohistochemistry (IHC) or fluorescent in
situ hybridization (FISH)

Expansion only: Histologically confirmed metastatic or recurrent, or locally advanced
triple-negative breast cancer as defined by the most recent American Society of
Clinical Oncology/College of American Pathologists (ASCO/CAP) guidelines.

3. Patient is not a candidate for endocrine based therapy, based on Investigator
judgement

4. Have a history of progressive disease despite prior therapy

5. Part 1: Have had at least 1 prior cytotoxic chemotherapy.

Part 2: Have had no more than 2 prior chemotherapy-inclusive regimens for locally
advanced or metastatic disease, unless approved by the Sponsor (no limit on prior
targeted anticancer therapies such as mechanistic target or rapamycin (mTOR) or CDK4/6
inhibitors, immune-oncology agents, tyrosine kinase inhibitors, or monoclonal
antibodies against CTL4 or VEGF.)

Expansion Cohort A (combination treatment in post-TROP2-ADC patients): Have received
TROP2-ADC therapy for unresectable locally advanced or metastatic disease.

Expansion Cohort B (ZEN003694 monotherapy): Have had at least 1 prior systemic therapy
for locally advanced or metastatic disease which may or may not have included a
TROP2-ADC.

Expansion Cohort C (combination treatment in TROP2-ADC-naive patients): Have had at
least 1 prior systemic therapy for locally advanced or metastatic disease and who have
not received prior TROP2-ADC therapy.

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

7. Part 2 and Expansion only: Measurable disease per RECIST version 1.1

Exclusion Criteria:

1. Documented germline mutations of BRCA1 or BRCA2

2. Parts 1 and 2 only: Evidence of disease progression during platinum treatment either
in the neoadjuvant or in the metastatic setting. For patients receiving platinum in
the neoadjuvant setting, at least 6 months must have elapsed between the last dose of
platinum-based treatment and enrollment

3. Part 2 only: Patients with inflammatory breast cancer

4. Current or anticipated use of medications known to be strong inhibitors or inducers of
CYP3A4 or substrates of CYP1A2 with narrow therapeutic windows. Strong inhibitors,
inducers or substrates must be discontinued at least 7 days prior to the first
administration of study drug.

5. Current or anticipated use within 7 days prior to the first administration of study
drug, or during the study, of strong P-gp inhibitors.

6. Use of oral Factor Xa inhibitors (i.e., rivaroxaban, apixaban, betrixaban, edoxaban
otamixaban, letaxaban, eribaxaban) and Factor IIa inhibitors (i.e., dabigatran). Low
molecular weight heparin is allowed

7. Prior anticancer therapy (chemotherapy, radiation, hormone therapy, immunotherapy or
investigational agent) within 3 weeks from the start of study drug (except for
nitrosoureas and mitomycin C within 6 weeks from start of study drug)

8. Parts 1 and 2 only: Radiation to >25% of the bone marrow

9. Treatment with a bone-targeted radionuclide within 6 weeks of first dose of study drug

10. Have previously received an investigational BET inhibitor (including previous
participation in studies with the Sponsor's drug, ZEN003694); except for patients in
Expansion Cohort B who received ZEN003694 monotherapy and are eligible to cross-over
to combination treatment

11. Prior treatment with a PARP inhibitor

12. QTcF interval > 470 msec

13. Insufficient recovery (i.e., has not recovered to at least Grade 1) from prior
treatment-related toxicities except for alopecia, fatigue and Grade 2 neuropathy

14. Non-healing wound, ulcer or bone fracture (not including a pathological bone fracture
caused by a pre-existing pathological bone lesion)

15. Parts 1 and 2 only: Brain metastases not adequately treated and clinically stable (at
the discretion of the Investigator) for at least 3 months prior to the start of study
treatment, unless a shorter interval is approved by the Sponsor's Medical Monitor

Expansion only: Progressive, symptomatic, or untreated brain metastases. CNS
metastases treated definitively with surgery and/or radiation must be radiographically
stable based on imaging at least 3 months after definitive treatment. CNS metastases
requiring steroid doses equivalent to prednisone doses >10 mg daily or an increase in
steroid doses due to CNS disease prior to consent are not eligible

16. Expansion only: Disease initially diagnosed with expression of estrogen receptor (ER)
or progesterone receptor (PR) as ≥5%

17. Expansion only: Patients treated with prior endocrine therapy