About this trial

The goal of this clinical trial is to learn if an investigational drug CP-383 works to treat advanced cancer. It will also learn about the safety of CP-383. The main questions if aims to answer are:

* Does CP-383 slow or stop the growth of cancer in patients with advanced cancer * What medical problems do participants have when taking CP-383 Researchers will test CP-383 in all kinds of cancers at various dose levels to determine what the best dose is to study further. Researchers will also see if certain cancers that have gene mutations respond better to CP-383

Participants will:

* Take CP-383 every day by mouth until the researcher learns whether CP-383 is helping slow or reduce the cancer growth * Visit the clinic weekly for the first 6 weeks for checkups and tests * Visit the clinic every 3 weeks thereafter for checkups and tests

Eligibility criteria

Qualifiers

Measurable or non measurable cancer that the research can assess for changes

Not eligible or able to take existing standard therapies for cancer

Availability of a part of a tumor for laboratory testing or willing to have a safe biopsy taken from a tumor

Diagnosed with locally advanced, recurrent or metastatic incurable disease

Disqualifiers

Inability to swallow pills

Known history of HIV, HCV, HBV unless cured, controlled with undetectable viral load

Active tumor in the brain

Clinically significant liver disease

Trial design

Treatments tested in this trial

  • CP-383

Treatment groups

150 Participants
are divided into 10 treatment groups

10

Treatment groups

See each treatment group below.

Locations

13
Colorado
Sarah Cannon Research Institute at HealthONE80218, Denver United States
Florida
Florida Cancer Specialists-Lake Nona32827, Orlando United States
Michigan
START Midwest49546, Grand Rapids United States
Missouri
Washington University63110, St Louis United States

Sponsors and collaborators

Tasca Therapeutics

Lead sponsor