Open-Label Study to Evaluate the Safety, Tolerability, PK, and Efficacy of INX-315 in Patients With Advanced Cancer

Incyclix Bio (Incyclix) is developing INX-315 as an oral, small molecule inhibitor of cyclin dependent kinase 2 (CDK2) for the treatment of human cancers. This first-in-human study is designed to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary antitumor activity of INX-315 in patients with recurrent advanced/metastatic cancer, including hormone receptor positive (HR+)/Human Epidermal Growth Factor Receptor 2 Negative (HER2-) breast cancer who progressed on a prior cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) regimen, and CCNE1-amplified solid tumors who progressed o

Trial Details

NCT ID
NCT05735080
Phase
PHASE1 / PHASE2
Sponsor
Incyclix Bio
Status
RECRUITING
Cancer Type
Ovarian Cancer
Interventions
  • INX-315
  • Fulvestrant
  • Abemaciclib
Locations (sample)
  • Orlando, Florida, United States|28.53834,-81.37924
  • Atlanta, Georgia, United States|33.749,-84.38798
  • Augusta, Georgia, United States|33.47097,-81.97484
  • Fort Wayne, Indiana, United States|41.1306,-85.12886
  • Boston, Massachusetts, United States|42.35843,-71.05977

Key Eligibility Criteria

  • Advanced unresectable or metastatic HR+/HER2- BC that has progressed following treatment with a CDK4/6 inhibitor in the adjuvant or advanced/metast…
  • Advanced/ metastatic platinum-resistant or platinum-refractory high grade serous epithelial ovarian cancer, fallopian tube cancer, or primary perit…
  • Advanced or metastatic solid tumor with known amplification of CCNE-1 that has progressed after standard therapy, been intolerant to or is ineligib…
  • At least one measurable lesion as defined by RECIST v1.1 that has not previously been irradiated

For full eligibility, visit ClinicalTrials.gov.

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