A Study of SY 5609, a Selective CDK7 Inhibitor, in Advanced Solid Tumors

Inclusion Criteria:

Age ≥ 18 years
Advanced Solid Tumors for which standard curative or palliative measures do not exist or are no longer effective (Group 1 only).
Postmenopausal women with HR-positive, HER2-negative advanced or metastatic breast cancer. Participants must have failed prior treatment with a cyclin-dependent kinase (CDK) 4/6 inhibitor in combination with hormonal therapy in a previous line of therapy (Group 2 only).
Participants with histologically or cytologically confirmed PDAC with measurable metastatic lesion(s) (Groups 3 and 4 only).
Participants must have at least 1 measurable lesion by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
All toxicities (except alopecia) from prior cancer treatments must have resolved to ≤ Grade 1 before enrollment.
For women of childbearing potential (WCBP): negative serum β human chorionic gonadotropin pregnancy test within 1 week before the first dose of SY 5609
Adequate organ and marrow function
Participants must be willing and able to comply with all aspects of the protocol
Participants must provide written informed consent before any study-specific screening procedures.
Albumin ≥ 3.0 grams/deciliters (g/dL) (Groups 3 and 4 only).

Exclusion Criteria:

Chemotherapy or limited field radiotherapy within 2 weeks, wide field radiotherapy within 4 weeks, or nitrosoureas or mitomycin C within 6 weeks before entering the study
Major surgery within 2 weeks before starting the study treatment, or not recovered to baseline status from the effects of surgery received > 2 weeks prior
Received any other investigational agents within 4 weeks before enrollment, or < 5 half-lives since completion of previous investigational therapy, whichever is shorter
Received previous noncytotoxic, US Food and Drug Administration-approved anticancer agent within previous 2 weeks, or < 5 half-lives since completion of previous therapy, whichever is shorter
Known brain metastases or carcinomatous meningitis
Immunocompromised participants with increased risk of opportunistic infections
Participants with known active or chronic hepatitis B or active hepatitis C infection. Participants with a history of hepatitis C virus (HCV) infection who have completed curative therapy for HCV at least 12 weeks before Screening and have a documented undetectable viral load at Screening are eligible for enrollment.

Baseline QT interval corrected (QTc) with Fridericia's method > 480 milliseconds

• NOTE: criterion does not apply to participants with a right or left bundle branch block (QTc interval)

Female participants who are pregnant or breastfeeding
History of clinically significant cardiac disease or clinically relevant uncontrolled cardiac risk factors
Uncontrolled intercurrent illness.
Poorly controlled ascites requiring paracentesis within 1 month prior to entering the study. (Groups 3 and 4 only)