Clin2
NCT04954599Possibly a fitRecruiting

CP-506 for hard-to-treat cancers with DNA repair defects

Unspecified Adult Solid Tumor, Protocol Specific

Treatments studied

Part of Cancer, Digestive system, Hormones & metabolism, Kidney & urinary, Skin, Women’s health & pregnancy clinical trials.

This Phase 1/2 study tests CP-506 in people with advanced solid tumors that have specific DNA repair problems (homologous recombination or Fanconi anemia-related defects). It may be used alone or combined with carboplatin or an immune therapy, aiming to shrink tumors or improve control when standard options are limited.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
126 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be age 18 or older and able to sign consent in writing
  • You must be expected to live at least 3 months and be well enough for treatment (ECOG 0–2)
  • You must be able to have at least one tumor biopsy for testing
  • Your blood counts and organ/liver/kidney function must be within safe limits (based on lab values)
  • Your cancer must have been proven by biopsy and be measurable on CT scan
  • Your tumor must have specific DNA repair defects (HR or Fanconi anemia-related), unless you match a qualifying exception for combination parts

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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