A Study of PRT2527 in Participants With Advanced Solid Tumors

This is a multicenter, open-label, dose-escalation and confirmation Phase 1 study of PRT2527, a CDK9 inhibitor, evaluating participants with selected advanced/metastatic sarcomas displaying a documented gene fusion, castrate resistant prostate cancer, hormone receptor positive HER2-negative breast cancer, advanced/metastatic non-small cell lung cancer, and solid tumors displaying MYC amplification. The study plan expects to evaluate approximately six dose levels of approximately 1-6 participants per dose level; however additional and/or intermediate dose levels may be explored. Taking into account pharmacokinetic and pharmacodynamic data from the preceding dose levels, the dose may be escalated until a dose limiting toxicity is identified. The total sample size will be approximately 30 patients for MTD and RP2D determination.

Inclusion criteria

• Tumor types under study

• Selected sarcomas with a documented gene fusion
• Castrate resistant prostate cancer (CRPC)
• Hormone receptor positive (HR+), HER2 negative (HER2-) breast cancer
• Non-small cell lung cancer (NSCLC)
• MYC amplified solid tumors
• Must have measurable disease per RECIST 1.1; participants with CRPC or sarcoma may have nonmeasurable but evaluable disease
• Eastern Cooperative Oncology Group (ECOG) Performance Score of 0 or 1
• Adequate organ function
• Must provide tumor tissue sample to the central laboratory for biomarker analysis
• Participants must have recovered from the effects of prior cancer-related therapy, radiotherapy, or surgery to ≤ Grade 1

Exclusion criteria

• Primary malignancies of the CNS, or uncontrolled CNS metastases, including impending spinal cord compression
• have a corrected QT interval >480 msec from prior or baseline
• have impaired cardiac function or clinically significant cardiac disease
• Treatment with strong inhibitors or inducers of CYP3A4
• Prior exposure to a CDK9 inhibitor
• History of another malignancy except for:

• Curatively treated malignancy with no known active disease
• Curatively treated non-melanoma skin cancer without evidence of disease
• Curatively treated carcinoma in situ without evidence of disease
• have undergone major surgery within 2 weeks prior to Week 1 Day 1
• have had chemotherapy, biologic therapy, targeted therapy, immunotherapy, extended-field radiotherapy, or investigational agents within 5 half-lives or 28 days (whichever is shorter) prior to administration of the first dose of study drug on Week 1 Day 1.