PhI/II PARP1 Selective Inhibitor IMP1734 in Pts w/AdvSolid Tumors

Cancer
Arash Rezazadeh Kalebasty
A First-in-human, Phase I/II, Open-label, Multi-center, Dose-Escalation, Dose-optimization, and Dose-expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Anti-tumor Activity of PARP1 Selective Inhibitor, IMP1734, as Monotherapy and in Combination in Participants with Advanced Solid Tumors
Corpus Uteri
Kidney
Other Male Genital
Other Urinary
Prostate

Study Description

This study will evaluate the preliminary efficacy of IMP1734 in patients with recurrent advanced/metastatic breast cancer, ovarian cancer and metastatic castrate resistant prostate cancer (mCRPC) with deleterious/suspected deleterious mutations of select homologous recombination repair (HRR) genes.

Eligibility

  • Adequate organ function
  • Life expectancy >= 12 weeks
  • Female subjects of childbearing potential and male subjects must agree to use an effective method of contraception from study entry up to 6 months after the last dose of IMP1734
  • Any investigational or approved anti-cancer therapies administered within 28 days/ before the first dose of IMP1734
  • Active or untreated central nervous system (CNS) metastases and/or carcinomatous meningitis.
  • An active hepatitis B/C infection
  • Unable to swallow oral medications OR have malabsorption syndrome or any other uncontrolled gastrointestinal condition that might impair the bioavailability
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