Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SCH-58500 + chemotherapy is a **combination therapy** consisting of **SCH-58500**, a recombinant, replication-deficient adenoviral vector expressing the human wild-type p53 tumor suppressor gene, administered together with standard **chemotherapy agents** (notably platinum-based agents such as carboplatin and paclitaxel)[3][5]. SCH-58500 functions as a gene therapy: by introducing wild-type p53 into cancer cells harboring mutant or absent p53, it aims to restore tumor suppressor function, induce cell-cycle arrest, and promote apoptosis. This regimen has been in clinical trials for solid tumors, especially recurrent ovarian, primary peritoneal, and fallopian tube cancers with mutant/aberrant p53[2][3]. Combination use is based on hypothesized synergy, as chemotherapy can induce p53-independent apoptosis, potentially enhancing tumor cell death when combined with p53 restoration[3][5].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on SCH-58500 + chemotherapy.